Bachelor-Studium Medical and Pharmaceutical Biotechnology

Wollen Sie helfen, die Lebensqualität von Millionen Patientinnen und Patienten weltweit dramatisch zu verbessern? Mit dem Bachelor-Studium Medical and Pharmaceutical Biotechnology haben Sie die Chance dazu.

Die Biotechnologie ist einer der am schnellsten wachsenden Forschungsbereiche der Welt – qualifizierte Expertinnen und Experten, Managerinnen und Manager und Forscherinnen und Forscher werden daher dringend gesucht. Als Absolventin oder Absolvent haben Sie das Fachwissen, um an bahnbrechenden Innovationen in der Biotechnologie mitzuarbeiten.

Das Studium

Der Studiengang wird in englischer Sprache geführt und umfasst naturwissenschaftliche, biomedizinische und technische Grundlagen in Form von Theorieblöcken und umfangreichen Laborpraktika.

Das Bachelor-Studium Medical and Pharmaceutical Biotechnology gliedert sich in folgende Teilgebiete:

Medizinische Biotechnologie

Vorlesungen und Laborübungen in den Bereichen biochemische Prozesse, Zell- und Molekularbiologie und Gentechnik inklusive der verschiedenen Analysetechniken bilden eine fundierte Wissensgrundlage. Zusätzlich erhalten Sie einen Einblick in die Humanmedizin und in die pharmazeutischen Wissenschaften, um die Arzneimittelwirkung und deren Herstellung zu verstehen.

Pharmazeutische Biotechnologie

Ein wichtiger Teilaspekt des Studiums: Lehrveranstaltungen, die die theoretischen Grundlagen und die praktische Umsetzung von Prozessen in der biopharmazeutischen Industrie behandeln. Das beinhaltet unter anderem die Auslegung von biopharmazeutischen Produktionsprozessen und die Grundlagen der Planung von dazugehörigen Produktionsstätten.

Die Lehrveranstaltungen im Labor stellen einen Musterprozess aus der Industrie repräsentativ dar.

Qualitätsmanagement

Fehler in der medizinischen und pharmazeutischen Industrie können lebensbedrohlich sein. Fundierte Kenntnisse im Bereich des Qualitätsmanagements sind daher unentbehrlich.

Wirtschaftliche Grundlagen

Neben den grundlegenden wirtschaftlichen Kenntnissen wird in Vorbereitung auf ein interdisziplinäres Arbeitsumfeld ein Fokus auf Kommunikation und HR gelegt.

Praktisches Arbeiten in Industrie und Forschung ist ebenfalls Teil der Ausbildung.

Zu den Forschungsprojekten

Geschichten aus dem Studium

Biotechnologie leicht erklärt

Die Biotechnologie ist eine interdisziplinäre Studienrichtung und integriert Wissensgebiete aus Medizin, Chemie, Biologie, Physik und Pharmazie. Erkenntnisse aus dieser multidisziplinären Wissenschaft werden integrativ genutzt: So werden als Beispiel biologische Systeme für die Herstellung von therapeutischen Molekülen oder Antikörpern für Bereiche wie die Krebstherapie eingesetzt.

Neue Ansätze für bestehende Krankheitsbilder

Durch die Bereitstellung innovativer medizinischer Wirkstoffe und Diagnoseverfahren hat sich die Biotechnologie in den letzten Jahren zu einer Schlüsseltechnologie der Zukunft entwickelt.

In der medizinischen Biotechnologie stehen zunehmend Stammzellen oder das Züchten von Geweben im Forschungsfokus. Dadurch lassen sich Krankheiten behandeln, die bisher als unheilbar galten.

Dementsprechend ist auch die medizinische und pharmazeutische Biotechnologie stark fachübergreifend. Sie konzentriert sich aber im Speziellen auf die Naturwissenschaften, auf Biomedizin und Technik.

Studium Medical and Pharmaceutical Biotechnology - Mann mit Pipette

Studium Medical and Pharmaceutical Biotechnology - Mann und Frau mit Notizbuch

Studium Medical and Pharmaceutical Biotechnology - Frau zeigt auf Landkarte

" Medizinisch-pharmazeutische Theorie kombiniert mit umfangreichen Laborpraktika: Unsere Studierenden bekommen eine Basis für ihren Einstieg in die Disziplin der Biotechnologie. Sie werden an der Lösung von Problemen mitarbeiten, auf die die Medizin heute keine befriedigenden Antworten hat. Sie bekommen die Chance, die Lebensqualität von Menschen weltweit zu verbessern. "
Studiengangsleiter Harald Hundsberger

Erfolgskonzept: Theorie + Praxis

Das Studium umfasst 3 Säulen:

1
1. Die Grundlagen
In den Semestern 1-4
Im Zuge Ihres Studiums setzen Sie sich mit allen Themen der medizinischen und pharmazeutischen Biotechnologie auseinander. Am Beginn des Studiums lernen Sie die Grundlagen der Naturwissenschaften, Biomedizin, Technik und Analytik kennen, um sich danach vertiefend mit der Materie auseinanderzusetzen. Darüber hinaus beschäftigen Sie sich auch mit Qualitätsmanagement, wirtschaftlichen Grundlagen, Kommunikation und Social Skills.
Außerdem verbringen Sie von Anfang an viel Zeit im Labor. In kleinen Gruppen machen Sie sich mit den wissenschaftlichen Abläufen vertraut und setzen das Gelernte gleich praktisch um.
2
2. Das Praktikumssemester
Im 5. Semester
Im 5. Semester absolvieren Sie ein 20-wöchiges Pflichtpraktikum. Mehr als 50 % der Medical and Pharmaceutical Biotechnology Studierenden absolvieren ihr Praktikum im Ausland bei internationalen Unternehmen, Forschungseinrichtungen oder Universitäten.
Vor und während des Praktikums werden Sie von uns betreut: Das Einzelcoaching mit unserer Praktikumskoordination ist darauf ausgerichtet, Ihre Stärken und Entwicklungspotenziale zu erkennen und darauf aufbauend gemeinsam den geeigneten Praktikumsplatz in einem nationalen oder internationalen Unternehmen zu finden.
Mehr Auslandserfahrung gefällig? Ab 2020 können Sie sich im 3. oder 4. Semester für ein Exchange-Semester an einer namhaften Universität wie dem Dublin Institute of Technology (Irland) oder der Linköping University (Schweden) entscheiden.
3
3. Die Spezialisierung
Im 6. Semester
Gegen Ende Ihres Studiums entscheiden Sie sich für eines der 2 Wahlfächer: Production of Therapeutic Proteins im Bereich der medizinischen Biotechnologie oder Drug Development Management im Bereich der pharmazeutischen Biotechnologie.
Das Ziel der medizinischen Biotechnologie ist es, beschädigte Zellen oder Organe nicht durch Transplantationen oder Dialyse zu behandeln, sondern durch natürliche Körperzellen. Die pharmazeutische Biotechnologie setzt sich mit der Produktherstellung und Handhabung auseinander. Antibiotika, die mithilfe von Mikroorganismen in großen Bioreaktoren hergestellt werden, sind Beispiele für traditionelle biotechnologische Produkte, die in der Pharmazie verwendet werden.

Studienplan

Was wird Sie im Studium genau erwarten? Der Studienplan gibt Ihnen eine Übersicht.
Klicken Sie auf die einzelnen Lehrveranstaltungen um nähere Informationen zu erhalten.

Course	SWS	ECTS
Introduction to Laboratory
Introduction to Laboratory Techniques	1	1
Introduction to Laboratory Techniques Module: Introduction to Laboratory Root module: Introduction to Laboratory Semester: 1 Course code: ILT1LB Contact hours per week: 1 ECTS: 1 Course Content: Basic techniques for laboratory-based scientific work Safety training and working with safety data sheets Introduction to laboratory equipment (glassware, etc.) Using laboratory equipment (e.g. scales, pH meters and spectrophotometers) Basic laboratory techniques Handling acids, bases and organic solvents Working with indicators Producing solutions and serial dilutions; calculating concentrations and estimating errors Course outcome: Upon completion of this course students are able to: perform the basic practical skills associated with day-to-day laboratory work, produce simple buffers and solutions, apply fundamental measurement techniques such as pH measurement, describe important safety regulations for laboratory work.
Basics of Physics
Applied Physics - Theory	2	3
Applied Physics - Theory Module: Basics of Physics Root module: Basics of Physics Semester: 1 Course code: APT1VO Contact hours per week: 2 ECTS: 3 Course Content: Fundamental physical values Equations of motion Equations of motion on a single plane Force and momentum Movements along an orbit Fields and energy Work and power Material physics Thermodynamics Geometric optics and waves Course outcome: Upon completion of this course students are able to: explain basic physical/scientific principles (f.e Thermodynamics,..), identify physical values that have a significant effect on biotechnological processes.
Applied Physics - Laboratory	3	4
Applied Physics - Laboratory Module: Basics of Physics Root module: Basics of Physics Semester: 1 Course code: APL1LB Contact hours per week: 3 ECTS: 4 Course Content: Working with devices Evaluating measurements and estimating errors Determining the molar mass of an unknown substance Laws of gases Heat transfer Conductivity Viscosity Spectrometers/goniometers Determining heat levels required for melting and evaporation Surface tension Molecular physics Absorption spectra Determining elementary charge Determining the Faraday constant Thermodynamics Course outcome: Upon completion of this course students are able to: perform and interpret simple, yet fundamental physical experiments, record and evaluate results of measurements, estimate errors in the results generated and write reports, explain fundamental physical processes on the basis of experiments.
Basics of Chemistry
Analytical Chemistry Laboratory	2	3
Analytical Chemistry Laboratory Module: Basics of Chemistry Root module: Basics of Chemistry Semester: 1 Course code: ACL1LB Contact hours per week: 2 ECTS: 3 Course Content: Basic day-to-day laboratory methods illustrated using analytical chemistry experiments Qualitative analysis methods: alkali, alkaline-earth and heavy metals, halogens, sulphates and carbonate detection Quantitative analysis methods: gravimetry, various forms of titration (acid-base, redox and complex titration) Equilibrium reactions, reaction kinetics Course outcome: Upon completion of this course students are able to: illustrate key chemistry concepts underpinning biotechnology, and demonstrate and apply this knowledge in examples (e.g. calculations for concentrations, reactions, pH values, etc.), carry out basic qualitative and quantitative analysis methods in the laboratory, apply basic day-to-day laboratory methods illustrated using analytical chemistry experiments.
Chemical Calculations	1	2
Chemical Calculations Module: Basics of Chemistry Root module: Basics of Chemistry Semester: 1 Course code: CC1VO Contact hours per week: 1 ECTS: 2 Course Content: Application-based calculations in a laboratory environment; determining and working with physical units Information on concentrations: calculating molarity, moles, percentages, normality and density Determining the stoichiometry of chemical reactions Classification of inorganic compounds Determining oxidation state; calculating pH values Course outcome: Upon completion of this course students are able to: apply basical calculations underpinning biotechnology in examples (e.g. calculations for concentrations, reactions, pH values, etc.), explain the fundamental scientific principles and laws of chemistry.
General and Inorganic Chemistry	3	4
General and Inorganic Chemistry Module: Basics of Chemistry Root module: Basics of Chemistry Semester: 1 Course code: GIC1VO Contact hours per week: 3 ECTS: 4 Course Content: Introduction to chemistry Importance of mass and units in the natural sciences Atoms and atomic models The periodic table Chemical bonds Chemical equilibrium Fundamentals of thermodynamics Reaction kinetics Properties of the elements and their inorganic compounds Acids and bases Redox reactions Solubility of salts Course outcome: Upon completion of this course students are able to: explain the fundamental scientific principles and laws of chemistry, illustrate key chemistry concepts underpinning biotechnology, and demonstrate and apply this knowledge in examples (e.g. calculations for concentrations, reactions, pH values, etc.).
Fundamentals in Mathematics
Applied Mathematics
Applied Mathematics - Theory	2	3
Applied Mathematics - Theory Module: Applied Mathematics Root module: Fundamentals in Mathematics Semester: 1 Course code: AMTI1VO Contact hours per week: 2 ECTS: 3 Course Content: Performing calculations with indices and logarithms (common and natural logarithms) Solving and applying quadratic equations and functions (linear, quadratic, polynomial, exponential and trigonometric [sin, cos and tan]) Differentiation (first and second derivatives) Integration (standard integrals) Basic principles of statistics: statistical analysis of measurements – samples and population, averages and their graphical representation empirical dispersion (range, linear distribution and empirical standard deviation) Course outcome: Upon completion of this course students are able to: use applied mathematics assumptions and carry out calculations, apply calculations and interpret examples out of biotechnology. practice
Applied Mathematics - Exercise	1	1
Applied Mathematics - Exercise Module: Applied Mathematics Root module: Fundamentals in Mathematics Semester: 1 Course code: AMEI1UE Contact hours per week: 1 ECTS: 1 Course Content: Practical exercises on lecture topics Course outcome: Upon completion of this course students are able to: use applied mathematics assumptions and carry out calculations, calculate and interpret examples out of biotechnology practice.
Introduction to Data Science I	1	1
Introduction to Data Science I Module: Fundamentals in Mathematics Root module: Fundamentals in Mathematics Semester: 1 Course code: IDSI1UE Contact hours per week: 1 ECTS: 1 Course Content: Fundamentals of IT Efficient usage of Microsoft Office applications, in particular Excel (table structures and calculations, graphical analysis of data) Software: commercial applications and open source (databases, statistics programs) Network architecture (company network, process control systems) Course outcome: Upon completion of this course students are able to: explain the basics of computer architecture, and data processing, use Microsoft applications (e.g. Excel) for data processing, anasylis and graphical presentation, explain the basics of data processing using different software applications.
Human Medicine I
Anatomy and Physiology	2	2
Anatomy and Physiology Module: Human Medicine I Root module: Human Medicine I Semester: 1 Course code: AP1VO Contact hours per week: 2 ECTS: 2 Course Content: Cells and their functions Basics of cell communication Tissue structure Anatomy and physiology of organs and blood Homeostasis in the human organism Course outcome: Upon completion of this course students are able to: explain the most important physiological processes in the human body, explain contributions of organs and systems to the maintenance of homeostasis.
Human Genetics	1	2
Human Genetics Module: Human Medicine I Root module: Human Medicine I Semester: 1 Course code: HG1VO Contact hours per week: 1 ECTS: 2 Course Content: Introduction to human genetics Mendelian inheritance Exceptions to Mendel’s laws Sexuality and heredity Multi-factor hereditary characteristics DNA and chromosomes Genetic polymorphism Replication, transcription and translation Mutation and hereditary diseases Population genetics Human evolution Course outcome: Upon completion of this course students are able to: illustrate the complexity and diversity of genetic processes, illustrate the connection between genetic information and cellular structure.
Microbiology
Applied Microbiology	1	2
Applied Microbiology Module: Microbiology Root module: Microbiology Semester: 1 Course code: AM1VO Contact hours per week: 1 ECTS: 2 Course Content: Introduction to microbiology Structure of bacterial cells Bacterial growth, kinetics, media and conditions for growth Growth monitoring and sterilisation Basics of bacterial metabolism Introduction to systematics, and archaea Course outcome: Upon completion of this course students are able to: explain bacterial cells and their growth, explain and evaluate growth monitoring methods and tools, explain and evaluate sterilization methods, illustrate principles of bacterial metabolism and principles of bacterial systematics, compare the differences between bacteria and archea.
Microbiological Working Techniques Laboratory	2	2
Microbiological Working Techniques Laboratory Module: Microbiology Root module: Microbiology Semester: 1 Course code: MWT1LB Contact hours per week: 2 ECTS: 2 Course Content: Students learn about basic techniques in microbiology: Producing media and plates Working under sterile conditions Cultivating and quantifying microorganisms and growth curves Staining methodes Microscopy Growth monitoring and sterilisation Course outcome: Upon completion of the course, students are able to: explain and apply the concept of sterility and recognize sources of contamination, perform basic microbiological methods like growing microorganisms, staining them, using the microscope etc., plan simple experiments, document the experiments properly, analyse critically method and outcome of experiments and sum it up in a written report, Sum up the critical analysis in a presentation and present the results.

Course	SWS	ECTS
Organic Chemistry
Organic Chemistry - Theory	2	3
Organic Chemistry - Theory Module: Organic Chemistry Root module: Organic Chemistry Semester: 2 Course code: OCT2VO Contact hours per week: 2 ECTS: 3 Course Content: Basic concepts of organic chemistry Chemistry of carbon Types of covalent bond Simple hydrocarbon compounds (alkanes, alkenes, alkynes and cycloalkanes) Functional groups in organic chemistry Aromatic and heterocyclic compounds 3D structures and classification of organic compounds (isomers, chirality and conformations) Reaction mechanisms: nucleophiles and electrophiles Substitution reactions Elimination reactions Polymerisation reactions Chemistry of amino acids Alkaloids and carbohydrates Presentation and discussion of basic scientific principles Course outcome: Upon completion of this course students are able to: explain the theoretical principles of organic chemistry, with a focus on component categories and reaction mechanisms, apply practical organic separation and detection skills and synthesise simple organic compounds, explain documentations on synthesis reactions and estimate the related risks.
Organic Chemistry - Laboratory	2	3
Organic Chemistry - Laboratory Module: Organic Chemistry Root module: Organic Chemistry Semester: 2 Course code: OCL2LB Contact hours per week: 2 ECTS: 3 Course Content: Basic organic chemistry techniques and basic synthesis Distillation and detection of alcohol Aspirin synthesis and analysis (thin-layer chromatography, analysing melting points, recrystallisation and UV detection) Producing soap and detergents Carbohydrate analysis Reaction kinetics Vitamin C detection Course outcome: Upon completion of this course students are able to: apply practical organic separation and detection skills and synthesise simple organic compounds, apply documentation on synthesis reactions and estimate the related risks, perform moderate complex laboratory experiments.
Biostatistics and Data Analysis in Biotechnology
Biostatistics	2	4
Biostatistics Module: Biostatistics and Data Analysis in Biotechnology Root module: Biostatistics and Data Analysis in Biotechnology Semester: 2 Course code: BST2VO Contact hours per week: 2 ECTS: 4 Course Content: Descriptive statistics: Averages (arithmetic, geometric and harmonic mean, and median) Dispersion (variance, standard deviation and coefficient of variation) Histograms and frequency distributions Box plots Simple linear regression Inferential statistics: Parametric tests (comparing independent and paired means, analysis of varianceNon-parametric tests (comparing independent and paired means, and analysis of variance) Tests on categorial data Course outcome: Upon completion of this course students are able to: explain the conceptual basis of statistical tests used in the field of biotechnology and life sciences, select suitable statistical tests for biotechnology questions, carry out such tests using relevant software, interpret and analyze the results obtained from biostatistical testing.
Introduction Data Science II	1	2
Introduction Data Science II Module: Biostatistics and Data Analysis in Biotechnology Root module: Biostatistics and Data Analysis in Biotechnology Semester: 2 Course code: IDSII2VO Contact hours per week: 1 ECTS: 2 Course Content: Employ tools for data integration and analysis (e.g. KNIME) for generating workflows aiming at reading in large amounts of data processing data visualizing data analyzing data Course outcome: Upon completion of this course students are able to: implement customized workflows for data analysis and integration, analyze real-life data relevant for life sciences.
Biophysics
Applied Biophysics	2	3
Applied Biophysics Module: Biophysics Root module: Biophysics Semester: 2 Course code: ABP2VO Contact hours per week: 2 ECTS: 3 Course Content: Introduction to electricity (Ohm’s law, Kirchhoff's circuit laws) electromagnetic waves physical principles and characteristics of synthetic and biological membranes, characterisation of biomembrane properties (Langmuir scales, photobleaching, electrons and atomic force microscopy) cell biophysics: cell characterisation methods (determining viscosity, patch clamp, cell electrophoresis, light microscopy, scanning electron microscopy, confocal fluorescence microscopy, cell impedance) radiophysics and its applications in nuclear medicine: principles of nuclear physics, dosimetry, nuclear medical procedures (gamma camera, PET, kinetic examinations, immunoscintigraphy) environmental biophysics. Certain topics will be examined in greater detail using sample calculations and demonstrations. Course outcome: Upon completion of this course students are able to: explain the physical principles and modern analytical methods that underlie biomedicine, explain the principles of nuclear physics, dosimetry, nuclear medical procedures (gamma camera, PET, kinetic examinations, immunoscintigraphy).
Biophysics Laboratory	2	3
Biophysics Laboratory Module: Biophysics Root module: Biophysics Semester: 2 Course code: BPL2LB Contact hours per week: 2 ECTS: 3 Course Content: Experiments will be performed on electricity, magnetism and the following basic biophysical phenomena: sound and sound propagation, phase transitions in polar fluids, characterisation of electrolytes, optical instruments and the characterisation of various sources of visible radiation, partial pressure in gaseous mixtures, radioactivity and adsorption. Course outcome: Upon completion of this course students are able to: apply/use analytical instruments and spectrum interpretation, use operating instructions and other common forms of documentation for the use and maintenance of instruments.
Human Medicine II
Human Diseases	1	1
Human Diseases Module: Human Medicine II Root module: Human Medicine II Semester: 2 Course code: HD2VO Contact hours per week: 1 ECTS: 1 Course Content: Basic physiological principles of regulation, adaptation and homeostasis Central pathophysiological processes in the human organism Key human illnesses, like - Cancer - Immune disorders - Hormonal disorders Course outcome: explain and analyze pathophysiological links, explain and classify common human illnesses, explain biotechnological treatment options.
Immunology and Medical Microbiology	2	2
Immunology and Medical Microbiology Module: Human Medicine II Root module: Human Medicine II Semester: 2 Course code: IMM2VO Contact hours per week: 2 ECTS: 2 Course Content: Structure and function of the immune system Humoral immune responses Cell-mediated immune responses Infectious diseases Human microbiome Viruses Bacterial pathogens Prions, viroids and parasites Options for prevention and therapy Course outcome: illustrate the most important components of the immune system and explain their interplay and communication, classify the different groups of pathogens and explain their interaction with the immune system, Explain preventive methods and therapies, analyze selected topics from immunology and medical microbiology and present them.
Microbiology and Pharmaceutical Production Environment
Microbiological Monitoring Laboratory	2	2
Microbiological Monitoring Laboratory Module: Microbiology and Pharmaceutical Production Environment Root module: Microbiology and Pharmaceutical Production Environment Semester: 2 Course code: MML2LB Contact hours per week: 2 ECTS: 2 Course Content: Basic microbial techniques Surface, air and water monitoring Isolating and identifying bacteria Disinfection and sterilisation Work in accordance with SOPs Preparing SOPs Course outcome: Upon completion of this course students are able to: illustrate the statutory regulations applicable to pharmaceutical production, explain the conditions required for microbial monitoring, exlain and apply surface, air and water monitoring methods in connection with microbes, explain and apply techniques for isolating and identifying microbes, prepare/write and apply standard operating procedures (SOPs), keep records of results, measurements, results of analytical tests and samples, independently plan simple experiments, analyse and present results of the experiments.
Introduction to Contamination Control and Clean Room Training	1	1
Introduction to Contamination Control and Clean Room Training Module: Microbiology and Pharmaceutical Production Environment Root module: Microbiology and Pharmaceutical Production Environment Semester: 2 Course code: CCCT2UE Contact hours per week: 1 ECTS: 1 Course Content: Introduction to statutory regulations applicable to pharmaceutical manufacturing Requirements for clean rooms Description of classes of clean room Principles and flow conditions in clean rooms Demonstration: putting on clean room clothing Familiarisation with and understanding special requirements for working in clean rooms Behaviour in clean rooms Microbiological and particle monitoring methods Minimising contamination in clean rooms Planning clean rooms Course outcome: Upon completion of this course students are able to: summarize the requirements for clean rooms and apply the knowledge for cleanroom concepts, compare/summarize the various classes of clean rooms, apply putting on clean room clothing correctly, compare/summarize and apply the specific requirements for working in clean rooms.
Molecular Biology of the Cell
Cell Biology	2	3
Cell Biology Module: Molecular Biology of the Cell Root module: Molecular Biology of the Cell Semester: 2 Course code: CB2VO Contact hours per week: 2 ECTS: 3 Course Content: Prokaryotic and eukaryotic cells (plant/animal cells) Cell organells: nucleus (chromosomes), endoplasmic reticulum, Golgi apparatus, mitochondria, peroxisomes, endosomes, and lysosomes Biological membrane systems and molecule transport (carrier etc.) Sorting of proteins (from the ER to the cell exterior/)lysosomes/PM Cytoskeleton, intermediate filaments, microtubules and actin Motorproteins Exocytosis and endocytosis Cell migration Mitosis (Cell Division) Course outcome: Upon completion of this course students are able to: compare prokaryotic and eukaryotic cells and between plant and animal cells, explain the function of the various cell compartments and cell organelles, the detailed mechanism of cell division, cell movement and cell clusters, and communication between cells.
Molecular Biology and Genetic Engineering - Theory	2	3
Molecular Biology and Genetic Engineering - Theory Module: Molecular Biology of the Cell Root module: Molecular Biology of the Cell Semester: 2 Course code: MBGE2VO Contact hours per week: 2 ECTS: 3 Course Content: Amino acids and proteins Structure and function of DNA Replication Transcription and checking transcripts Translation Recombination DNA sequencing and PCR Isolating nucleic acids Cloning strategies Vector systems and expressions of recombinant proteins Course outcome: Upon completion of this course students are able to: explain genetic processes such as replication, transcription, translation and recombination, illustrate the theoretical principles for working with nucleic acids, cloning genes and expressing recombinant proteins.

Course	SWS	ECTS
Laboratory Skills for Biotechnology
Instrumental Analytics - Theory	1	2
Instrumental Analytics - Theory Module: Laboratory Skills for Biotechnology Root module: Laboratory Skills for Biotechnology Semester: 3 Course code: IAT3VO Contact hours per week: 1 ECTS: 2 Course Content: • Centrifugation • UV-vis spectroscopy • Fluorescence spectroscopy • Electrophoresis • Chromatography • Mass spectrometry Course outcome: • explain the physical principles and modern analytical methods that underlie biomedicine, • compare main analytical technologies in the area of Biotechnology, Biochemistry and Molecular Biology (f.e. genetic engineering).
Instrumental Analytics - Laboratory	2	3
Instrumental Analytics - Laboratory Module: Laboratory Skills for Biotechnology Root module: Laboratory Skills for Biotechnology Semester: 3 Course code: IAL3LB Contact hours per week: 2 ECTS: 3 Course Content: • Determining cytotoxicity using luminescence spectrometry • PCR and qPCR • Fluorescence spectroscopy • DNA/protein quantification, UV/vis spectroscopy • Chromatography • Performance qualification for analytical instruments Course outcome: • apply main analytical technologies in the area of Biotechnology, Biochemistry and Molecular Biology (f.e. genetic engineering), • work with nucleic acids, • apply calibration and maintain measuring devices, • carry out practical experiments in a quality-controlled environment.
Genetic Engineering Laboratory	2	3
Genetic Engineering Laboratory Module: Laboratory Skills for Biotechnology Root module: Laboratory Skills for Biotechnology Semester: 3 Course code: GEL3LB Contact hours per week: 2 ECTS: 3 Course Content: • Working with E. coli • Transforming E. coli • Plasmid preparation • Restriction digestion • DNA gel electrophoresis • Calibrating pipettes • Spectrophotometrically measurements Course outcome: • apply calibration and maintain measuring devices (f.e.microlitre volume), • perform basic experiments of molecular biology.
Theoretical and Practical Biochemistry
Biochemistry - Theory	3	4
Biochemistry - Theory Module: Theoretical and Practical Biochemistry Root module: Theoretical and Practical Biochemistry Semester: 3 Course code: BCHT3VO Contact hours per week: 3 ECTS: 4 Course Content: The properties of water and aqueous solutions Fundamentals of biological thermodynamics Nucleotides and nucleic acids Amino acids proteins Carbohydrates Lipids and biological membranes Enzymes Introduction to metabolsim Glycolysis, gluconeogenesis and glycogen metabolism Citric acid cycle Oxidative phosphorylation and photosynthesis Fat metabolism Amino acid metabolism Nucleotide metabolism Regulation of metabolic pathways in complex organisms Metabolic disorders, the molecular principles behind them, and therapies Course outcome: Upon completion of this course students are able to: explain the basic physical chemistry principles behind living systems, distinguish between the structural principles of biomolecules in terms of their chemical basis, delineate and asses the metabolic pathways used to produce energy and synthesize biomolecules within organism, explain regulation and the interplay between the most important metabolic pathways.
Biochemistry - Laboratory	2	3
Biochemistry - Laboratory Module: Theoretical and Practical Biochemistry Root module: Theoretical and Practical Biochemistry Semester: 3 Course code: BCHL3LB Contact hours per week: 2 ECTS: 3 Course Content: Producing buffers Biochemistry techniques: dialysis, gel filtration and methods for determining protein content SDS-PAGE, western blotting for serums and quantitative ELISA Enzyme kinetics Risk analysis and evaluation of corresponding experiments Course outcome: Upon completion of this course students are able to: apply state-of-the-art methods for isolating and analyzing biomolecules, use methods learned in the Biostatistics course to analyze the data obtained, analyze and interpret the experimental data generated.
Applied Bioinformatics
Bioinformatics	2	3
Bioinformatics Module: Applied Bioinformatics Root module: Applied Bioinformatics Semester: 3 Course code: BIN3VO Contact hours per week: 2 ECTS: 3 Course Content: Key biological databases and online tools: NCBI, EBI and ExPASy Tools for visualising biomolecules Sequence comparison and alignment of biomolecules Bioinformatics tools used in functional genome analysis Bioinformatics tools used in proteomics Bioinformatics tools in the laboratory: primer design, in silico cloning and calculating biomolecular properties Course outcome: Upon completion of this course students are able to: explain, analyse and interpret sequential and structural differences of biomolecules, use internet tools to analyze the evolutionary relatedness of proteins and nucleic acids, use internet tools and software to analyze the structure, function and properties of biomolecules, explain and use tools for daily laboratory work such as primer design and in silico cloning.
Medical Biology
Cell Physiology and Medical Molecular Biology	2	3
Cell Physiology and Medical Molecular Biology Module: Medical Biology Root module: Medical Biology Semester: 3 Course code: CPMB3VO Contact hours per week: 2 ECTS: 3 Course Content: Cell communication and signal transduction Regulating the cell cycle (G1, DNA synthesis and mitosis) Regulating apoptosis Ion channels and transporters Physiology of nerve cells Structure and physiology of epithelia Stem cells, proliferation and cell differentiation Course outcome: Upon completion of this course students are able to: explain general physiological processes in eukaryotic cells, classify and carry out mechanistic evaluation of individual cell communication and signal transduction pathways.
Cell Culture Techniques	1	1
Cell Culture Techniques Module: Medical Biology Root module: Medical Biology Semester: 3 Course code: CCT3VO Contact hours per week: 1 ECTS: 1 Course Content: Cell culture laboratory equipment: clean benches, incubators, centrifuges and light microscopes Biological safety and hazardous substances Growth media and components Transfection, transduction and transformation Primary cells and cell lines Flow cytometer Confocal microscopy RNAi techniques and the CRISPR/Cas system Assay formats in applied cell biology research Cell disruption and analysis Cell-based testing systems for screening of active ingredients Course outcome: Upon completion of this course students are able to: explain the theoretical principles as well as the advantages and disadvantages of the most important (and most often used) techniques and technologies in modern cell biology.
Cell Culture Laboratory I	2	3
Cell Culture Laboratory I Module: Medical Biology Root module: Medical Biology Semester: 3 Course code: CCL3LB Contact hours per week: 2 ECTS: 3 Course Content: Working under sterile conditions Waste disposal and autoclaving Determining cell counts Thawing and freezing eukaryotic cells Growth curves of eukaryotic cells Passaging suspension cultures and adherent cells Genetic manipulation of cell lines Light and fluorescence microscopy Course outcome: Upon completion of this course students are able to: use equipment and devices used in cell biology research in order to address scientific questions, independently apply fundamental experimental techniques used in cell biology research.
Fundamentals of Engineering
Bioprocess Technology Theory I	1	1
Bioprocess Technology Theory I Module: Fundamentals of Engineering Root module: Fundamentals of Engineering Semester: 3 Course code: BTT3VO Contact hours per week: 1 ECTS: 1 Course Content: Introduction to bioprocess technology Hydrostatics Hydrodynamics Pumping fluids and characteristic curves of pumps Piping Net Positive Suction Head and Total Dynamic Head Course outcome: Upon completion of this course students are able to: explain Hydrostatics and solve corresponding examples, understand Hydrodynamics and solve corresponding examples, apply the Bernoulli-equation to ideal and realistic calculations and solve corresponding tasks, apply/use calculations of Total Dynamic Head and Net Positive Suction Head for instalments.
Measurement and Control Systems I	1	1
Measurement and Control Systems I Module: Fundamentals of Engineering Root module: Fundamentals of Engineering Semester: 3 Course code: MCSI3VO Contact hours per week: 1 ECTS: 1 Course Content: Basics of sensor technology and sensor/control engineering, and their application in biotechnology Fundamentals of electrotechnology Measuring systems (conversion and classification) Sensor design (interfaces, signal processing) Sensor systems (pressure, flow and temperature sensors) Control engineering systems (PI, PD and PID controllers) Course outcome: Upon completion of this course students are able to: explain the fundamental measurement principles of electronics and their application in controllers for bioprocess technology, explain and interpret technical drawings and circuit diagrams, correctly carry out the properties of materials in use.
Quality Management and GLP
Introduction to Quality Management	1	1
Introduction to Quality Management Module: Quality Management and GLP Root module: Quality Management and GLP Semester: 3 Course code: IQM3VO Contact hours per week: 1 ECTS: 1 Course Content: Quality assurance in companies by means of procedural instructions underpinned by specifications and SOPs Quality management in companies (vision, mission, strategy) Quality management cycle Quality controls Indicators Quality assurance Practical exercises in which students draw up and present simple specifications, SOPs or procedural instructions Course outcome: Upon completion of this course students are able to: explain and interpret quality assurance processes for pharmaceuticals, explain and interpret the key statutory regulations applicable to the production of biopharmaceuticals.
GLP/GMP - Theory	1	1
GLP/GMP - Theory Module: Quality Management and GLP Root module: Quality Management and GLP Semester: 3 Course code: GGT3VO Contact hours per week: 1 ECTS: 1 Course Content: Statutory regulations on GLP and the set-up of GLP test laboratories Responsibilities, test set-ups and carrying out studies in accordance with GLP Overview of statutory regulations on GLP and the set-up of production facilities Core aspects of quality management at production facilities in accordance with GLP Quality assurance for biopharmaceuticals produced in accordance with GLP GLP/GMP regulations during biotechnology research and development processes Course outcome: Upon completion of this course students are able to: explain and can apply GLP regulations by planing and generating of study plans, explain and apply Quality Controll at production facilities in accordance with GMP, illustrate and apply GMP regulations by planing and preparing of documents.
Practical Training in Industry
Practical Training Application and Preparation	1	1
Practical Training Application and Preparation Module: Practical Training in Industry Root module: Practical Training in Industry Semester: 3 Course code: PAP3SE Contact hours per week: 1 ECTS: 1 Course Content: Writing CVs and covering letters Career and internship opportunities in industry and research Coaching support with internship applications Course outcome: Upon completion of this course students are able to: generate application documents, choose a suitable place for Practical Training Semester (PTS), illustrate different career paths in biotechnology.

Course	SWS	ECTS
Cell and Tissue Engineering
Cell Culture Laboratory II	3	5
Cell Culture Laboratory II Module: Cell and Tissue Engineering Root module: Cell and Tissue Engineering Semester: 4 Course code: CLLII4LB Contact hours per week: 3 ECTS: 5 Course Content: Theoretical principles: - Cell-based testing of active ingredients - Organotypic 3D cultivation and tissue engineering - Personalised medicine Relationship between genotypes and sensitivity to active ingredients - Tissue engineering methods - Cellular microreactors and their application Practical work: - Engineering blood vessels - Engineering organotypic 3D microtumours - Analysing and quantifying the invasive behaviour of tumour cells and 3D microtumours - Confocal immunofluorescence microscopy: determining the intra-cellular localisation of proteins - Reporter gene assays: quantifying activity in transcription factors Course outcome: Upon completion of this course students are able to: discuss key topical issues in cell biology research, independently plan and carry out complex experimental work, perform qualification and validation of experimental techniques, analyse and interpret data and results.
Scientific Skills	2	3
Scientific Skills Module: Cell and Tissue Engineering Root module: Cell and Tissue Engineering Semester: 4 Course code: SSK4SE Contact hours per week: 2 ECTS: 3 Course Content: Literature databases with a focus on NCBI and PubMed Academic journals and the peer review process Rating, impact factor and academic quality Structure and content of scientific papers Writing academic articles: wording, style and structure (title, introduction, material and methods, results, discussion, references and acknowledgements) Guidelines for the title and introduction Presenting data and results Interpreting and discussing results, taking into account current knowledge Using software to manage references (Endnote, Reference Manager and Mendeley) Original scientific papers, review articles, bachelor, master and doctoral theses Funding scientific work Preparing and submitting research proposals Presenting work packages, milestones and targets Austrian and international funding bodies Fundamentals of scientific communication Communicating with stakeholders Careers in science and research: academia and industry Course outcome: Upon completion of this course students are able to: carry out literature searches in databases, summarise and evaluate the results of experiments in a scientific paper and prepare the paper for publication, explain the peer review process, take part in active scientific discourse.
Pharmaceutical Production Processes
Protein Purification and Bioprocess Technology
Biochemical Analytics, Protein Purification	2	3
Biochemical Analytics, Protein Purification Module: Protein Purification and Bioprocess Technology Root module: Pharmaceutical Production Processes Semester: 4 Course code: BAPP4VO Contact hours per week: 2 ECTS: 3 Course Content: This course outlines the principles behind the following methods: Chromatographic principles (IEX, affinity, HIC, SEC, partition and adsorption) Chromatographic equipment (HPLC, FPLC, GC and SCFC) including detectors Proteomics methods (electrophoresis including CE, and blotting) Spectroscopy methods (UV-Vis, IR, Raman, MS including ionisation, and NMR) Course outcome: Upon completion of this course students are able to: explain analytical methods in chromatography, spectroscopy, electrophoresis, explain and develop analytical processes using principles of chromatography, electrophoresis and spectroscopy.
Equipment and Production Design	2	3
Equipment and Production Design Module: Protein Purification and Bioprocess Technology Root module: Pharmaceutical Production Processes Semester: 4 Course code: EPD4VO Contact hours per week: 2 ECTS: 3 Course Content: Components in biopharmaceutical production facilities (WFI and ultra-pure steam; utilities, description of equipment for the production of cell inoculants, bioreactors) including exercises Downstream equipment Instrumentation in pharmaceutical production facilities QM element: preparing device specifications Course outcome: Upon completion of this course students are able to: illustrate the key components of biotechnology facilities and installations and describe their basic functions, summarize and apply the basic steps involved in commissioning a biotechnology production facility, explain the principles of upstream and downstream processes, apply principles of typical equipment and production design to typical biopharmaceutical tasks.
Bioprocess Technology Theory II	2	4
Bioprocess Technology Theory II Module: Protein Purification and Bioprocess Technology Root module: Pharmaceutical Production Processes Semester: 4 Course code: BPTTII4VO Contact hours per week: 2 ECTS: 4 Course Content: Fundamentals of Reactor Design Fundamentals of Mass Balance Fundamentals of Heat Balance Kinetics in Bioprocess Technology Sterilisiation Techniques Principles of Fermentation Course outcome: Upon completion of this course students are able to: explain and solve problems correlating with mass and heat balances, apply rules of bioprocess kinetics to typcial tasks like fermentation development, explain and apply typical sterilisation procedures, explain and apply principles of balancing, sterilisation and bioprocess kinetics.
Fermentation and Bioseparation Laboratory, Data Analysis	4	6
Fermentation and Bioseparation Laboratory, Data Analysis Module: Pharmaceutical Production Processes Root module: Pharmaceutical Production Processes Semester: 4 Course code: FBL4LB Contact hours per week: 4 ECTS: 6 Course Content: Structure and operation of fermentation in bioreactors Conducting fed-batch fermentation with bacteria Process management and problem-solving In-process and offline analytics Measuring, evaluating and interpreting process parameters during fermentation, and their effect on biological aspects of processes Practical skills required for working with bioreactors under sterile conditions Handling analytical devices (glucose measuring devices, FPLC, etc.) Course outcome: Upon completion of this course students are able to: use scale tasks, pipeline system configurations, pump calculations, power inputs in stirred tanks, and heat and mass balancing at biopharmaceutical plants, use calculations for the configuration and management of biopharmaceutical processes, explain the connections between technology and microbiology, establish quality management principles in pharmaceutical processes.
Applied Quality Management
GLP/GMP - Seminar	2	3
GLP/GMP - Seminar Module: Applied Quality Management Root module: Applied Quality Management Semester: 4 Course code: GGL4SE Contact hours per week: 2 ECTS: 3 Course Content: Core aspects of GMP/GLP in practice / QM Documentation (GDP) Presentation of a GLP laboratory set-up / Theoretical background Detailed describing of experiments and procedures in Study Plan and Study Audit Report (Audit during the laboratory week) Lot Data Sheets Compiling the expected results Writing study reports; SOPs; Course outcome: Upon completion of this course students are able to: identify the basic statutory regulations applicable to biopharmaceutical manufacturing, explain quality assurance processes for pharmaceuticals.
Genetic Engineering Laboratory under GLP	2	3
Genetic Engineering Laboratory under GLP Module: Applied Quality Management Root module: Applied Quality Management Semester: 4 Course code: GELG4LB Contact hours per week: 2 ECTS: 3 Course Content: Advanced molecular biology Independently carrying out a complex experiment planned and prepared by students in GLP/GMP seminar Techniques: DNA isolation, restriction analysis; quantification of DNA; DNA Extraction from agarose gel, agarose electrophoresis, ligation, preparation of competent cells, transformation and colony PCR / GLP documentation of all procedural steps Approaches to GLP-compliant documentation of results generated in experiments and summarising the results in study report Experiments will be carried out in the form of a GLP study Laboratory Audit Course outcome: Upon completion of this course students are able to: independently apply knowledge of regulatory frameworks in practice, and draft SOPs and study plans carry out simple qualification of measuring devices in a quality-controlled environment generate plans for the most common methods and analytical techniques used in molecular biology, apply them under GLP-compliant conditions, and analyse and record the results

Course	SWS	ECTS
Practical Training in Industry
Practical Training Semester	0	25
Practical Training Semester Module: Practical Training in Industry Root module: Practical Training in Industry Semester: 5 Course code: PTS5BOPR Contact hours per week: 0 ECTS: 25 Course Content: The practical training semester is spent in a company or research institution in the field of biotechnology and students learn to know the daily work life in these institutions. Course outcome: Upon completion of this course students are able to: work in the professional field of biotechnology.
Scientific Methods and Tools
Bachelor Paper and Bachelor Exam
Bachelor Seminar I	1	5
Bachelor Seminar I Module: Bachelor Paper and Bachelor Exam Root module: Scientific Methods and Tools Semester: 5 Course code: BAI5BASE Contact hours per week: 1 ECTS: 5 Course Content: Definition of topic for bachelor paper Content and structure of bachelor paper Writing a bachelor paper proposal in accordance with the applicable guidelines Course outcome: Upon completion of this course students are able to: independently write a bachelor paper proposal of the required length which adheres to academic guidelines by a pre-agreed deadline, establish links between their chosen topic and the wider subject area generate and correctly formulate a research question and develop a suitable research methodology, critically reflect on their approach (research questions and methodology).

Course	SWS	ECTS
Pharmaceutical Sciences
Pharmacology	2	4
Pharmacology Module: Pharmaceutical Sciences Root module: Pharmaceutical Sciences Semester: 6 Course code: PHM6VO Contact hours per week: 2 ECTS: 4 Course Content: Pharmacokinetics Pharmacodynamics Pharmacology of the autonomic nervous system Antimicrobial substances Antiviral substances Chemotherapy Allergies and asthma Coagulation Cardiovascular pharmacology Steroid hormones Metabolic syndrome Course outcome: explain the interaction of substances with cells and tissue, explain how medications interfere with signalling pathways in order to produce a therapeutic effect, explain unwanted side effects of medications, explain the administration, spread, excretion, decomposition and toxicity of medications in the human body, differentiate between various categories of substances and mechanisms of action.
Current Issues in Molecular Medicine	2	3
Current Issues in Molecular Medicine Module: Pharmaceutical Sciences Root module: Pharmaceutical Sciences Semester: 6 Course code: CIMM6SE Contact hours per week: 2 ECTS: 3 Course Content: External specialists will be invited to speak about current issues in molecular medicine, giving an insight into their specialist area and working environment. Course outcome: Upon completion of this course students are able to use practical examples from research and industry to evaluate and solve problems associated with substance development.
Project Management
Project Management in Life Sciences	2	3
Project Management in Life Sciences Module: Project Management Root module: Project Management Semester: 6 Course code: PM6VO Contact hours per week: 2 ECTS: 3 Course Content: Projects: targets, focal points, structural plan, definition of work packages, cost budgeting and environmental analysis Corporate organisational structures Project controlling Project reporting and closing Project scorecard Final project report Crises in projects Good Clinical Practice Course outcome: Upon completion of this course students are able to: plan, manage and implement projects in an international environment, plan and execute tasks in the complex, interdisciplinary setting of the pharmaceuticals industry, plan / generate and evaluate a set-up for the implementation of clinical trials, and assess the regulations that underlie them.
Elective Module 1: Production of Therapeutic Proteins
Journal Club for Current Issues
Journal Club for Current Issues	1	2
Journal Club for Current Issues Module: Journal Club for Current Issues Root module: Elective Module 1: Production of Therapeutic Proteins Semester: 6 Course code: S1_JCCI6SE Contact hours per week: 1 ECTS: 2 Course Content: Literature research on the latest trends in the relevant field Reviewing relevant literature Presenting results of the literature review Discussion of contents of the selected literature Course outcome: Upon completion of this course students are able to: structure and analyse scientific articles in their specialist field and use them for their thesis, apply literature research in the relevant field.
Validation and Biomaterials
Introduction to Validation	1	2
Introduction to Validation Module: Validation and Biomaterials Root module: Elective Module 1: Production of Therapeutic Proteins Semester: 6 Course code: S1_IIV6VO Contact hours per week: 1 ECTS: 2 Course Content: Fundamentals of validation: legal principles, validation pyramid, equipment qualification (IQ, OQ, PQ) Basics of test validation (e.g. sensitivity, reproducibility and robustness) Basics of facility validation including an exercise involving the preparation of user requirements specifications and functional specifications Course outcome: Upon completion of this course students are able to: explain and use standard terminology such as qualification and validation in the biotechnology industry, explain and apply fundamentals of validation.
Material Science and Biomaterials	1	2
Material Science and Biomaterials Module: Validation and Biomaterials Root module: Elective Module 1: Production of Therapeutic Proteins Semester: 6 Course code: S1_MSB6VO Contact hours per week: 1 ECTS: 2 Course Content: Classification of chemical substances, general materials science and the properties of materials Material selection for specific facilities and pieces of equipment Biocompatibility of materials Metals and their applications in process technology Plastics and their applications in process technology Course outcome: Upon completion of this course students are able to: explain biopharmaceutical quality documentation and use documentation for new requirements, analyse the properties of materials and select the correct materials for a specific task.
Recombinant Protein Technologies
Measurement and Control Systems II	1	2
Measurement and Control Systems II Module: Recombinant Protein Technologies Root module: Elective Module 1: Production of Therapeutic Proteins Semester: 6 Course code: S1_MSCII6VO Contact hours per week: 1 ECTS: 2 Course Content: Principles of control technology User software applications for control systems: analogue and digital signals, analogue-to-digital and digital-to-analogue converters, microcontrollers, control systems (programmable controllers); incl. independent programming and testing Process control technology theory: the individual components and functions of a biotechnology process control system Course outcome: Upon completion of this course students are able to: analyse control systems and apply them to new situations, create and use control and regulation algorithms.
Pharmaceutical Protein Production Systems	1	2
Pharmaceutical Protein Production Systems Module: Recombinant Protein Technologies Root module: Elective Module 1: Production of Therapeutic Proteins Semester: 6 Course code: S1_PPPS6VO Contact hours per week: 1 ECTS: 2 Course Content: The components of a biotechnology facility, and their installation, commissioning and correct operation Biotechnology production processes illustrated using examples of selected microbial production systems (E. coli, yeasts) and eukaryotic production systems (CHO) Course outcome: Upon completion of this course students are able to: apply and analyse biotechnology processes, explain biotechnology production facilities,
Elective Module 2: Drug Development Management
Journal Club for Current Issues
Journal Club for Current Issues	1	2
Journal Club for Current Issues Module: Journal Club for Current Issues Root module: Elective Module 2: Drug Development Management Semester: 6 Course code: S2_JCCI6SE Contact hours per week: 1 ECTS: 2 Course Content: Literature search on the latest trends in the relevant field Reviewing relevant literature Presenting results of the literature review Discussion of contents of the selected literature Course outcome: Upon completion of this course students are able to: structure and analyse scientific articles in their specialist field and use them for their thesis, apply literature research in the relevant field.
Management and Marketing
Principles of Management and Marketing	2	3
Principles of Management and Marketing Module: Management and Marketing Root module: Elective Module 2: Drug Development Management Semester: 6 Course code: S2_PMM6VO Contact hours per week: 2 ECTS: 3 Course Content: Business objectives and principles Economics (market structures, legal framework) Marketing (market analyses, market strategies) Management and human resource management Management principles Recruitment and training Accounting and management control Financing, procurement, production Operational management Course outcome: Upon completion of this course students are able to: explain and implement marketing strategies in the pharmaceutical industry, apply theoretical marketing knowledge in practice-related situations, anaylse relationships in complex decision-making scenarios and develop effective courses of action as part of a team, illustrate and analyse competition between rival companies, explain and apply the basics of strategic marketing planning.
Biomedical Regulations
Clinical Studies and GCP	1	3
Clinical Studies and GCP Module: Biomedical Regulations Root module: Elective Module 2: Drug Development Management Semester: 6 Course code: S2_CLG6VO Contact hours per week: 1 ECTS: 3 Course Content: Pharmacovigilance, drug safety Informed consent Drug development Documentation Course outcome: Upon completion of this course students are able to: carry out independent critical evaluation of the design and execution of clinical trials, apply the fundamental principles of good clinical practice (GCP) in line with international standards, as well as basic principles of quality and project management.
Drug Regulatory Affairs	1	2
Drug Regulatory Affairs Module: Biomedical Regulations Root module: Elective Module 2: Drug Development Management Semester: 6 Course code: S2_DRA6VO Contact hours per week: 1 ECTS: 2 Course Content: Approval of a new product Efficacy, safety and patient information Labelling of packaging Maintaining approval Required documentation, options for making changes to approvals Course outcome: Upon completion of this course students are able to: explain and apply domestic and international regulatory frameworks for the approval of drugs and medical products, illustrate the content of a marketing approval dossier, explain and apply product information and labelling guidelines.
Scientific Methods and Tools
Bachelor Paper and Bachelor Exam
Bachelor Seminar II and Bachelor Paper	1	8
Bachelor Seminar II and Bachelor Paper Module: Bachelor Paper and Bachelor Exam Root module: Scientific Methods and Tools Semester: 6 Course code: BAII6BASE Contact hours per week: 1 ECTS: 8 Course Content: Composing the bachelor paper based on the research proposal Preparation of bachelor paper including project planning Topic-focused literature research Applying content-related and academic requirements Presentation of selected chapters Course outcome: Upon completion of this course students are able to: independently generate an academic paper in accordance with content-related and formal academic requirements, critically analyse selected chapters of their paper and their significance, discuss the applicability of the results to other cases and questions.
Bachelor Exam	0	2
Bachelor Exam Module: Bachelor Paper and Bachelor Exam Root module: Scientific Methods and Tools Semester: 6 Course code: BEX6AP Contact hours per week: 0 ECTS: 2 Course Content: Presentation of bachelor paper (and project), Oral examination on the bachelor paper (in accordance with section 16 Fachhochschul-Studiengesetz [University of Applied Sciences Studies Act]), and the links to related subjects on the curriculum (in accordance with section 16 University of Applied Sciences Studies Act). Course outcome: Upon completion of this course students are able to: present their bachelor paper and the question they addressed in a manner appropriate to the target audience, and defend the paper before an expert committee, examine the significance of the findings for professional practice and research, and present supporting arguments, answer follow-up questions on degree-programme subjects and the links between them, and justify their answers.

Besonderheiten

Warum sollten Sie sich für das Medical and Pharmaceutical Biotechnology in Krems entscheiden?

Der Bachelor-Studiengang „Medical and Pharmaceutical Biotechnologie“ ist weltweit einer der breitesten Biotechnologiestudiengänge in der roten Biotechnologie und daher mit vielen internationalen Master-Studiengängen im biomedizinischen Bereich kompatibel.

Aufgrund der zahlreichen Forschungsprojekte fließen immer wieder aktuelle Themen der internationalen Forschung in den Lehrplan ein und im Zuge von Forschungsprojekten werden auch Bachelor- und Master-Arbeiten am Institut für Biotechnologie verfasst.

International studieren und arbeiten

Mit Ihrem englischsprachigen und praxisorientierten Bachelor-Studium legen Sie den Grundstein für eine internationale Karriere. Die Hälfte der Vorlesungen und Übungen werden von Lehrenden mit Erfahrungen im Forschungs- oder Wirtschaftsbereich gehalten. Viele davon kommen von bekannten Universitäten, führenden Forschungsinstitutionen und Forschungsunternehmen in Österreich und 22 anderen Ländern.

Unsere Hochschule hat viele Forschungskooperationen, darunter einige der Top-Universitäten auf dem Gebiet der Biotechnologie: Karolinska Institute in Stockholm, Harvard University, Garvan Institute in Sydney und weitere 300 weltweit. Diese guten Beziehungen ermöglichen Ihnen vielfältige Chancen des Austausches und der internationalen Erfahrungen.

Ein weiteres Highlight: Das Institut organisiert jährlich eine wissenschaftliche Konferenz. Internationale Sprecher aus Forschung und Industrie interagieren mit unseren Studierenden und Alumni.

Zur Life Sciences Week

Im Labor: Übung macht den Meister

Das Erlernen von praktischen Fähigkeiten – die Laborpraxis – ist neben der Vermittlung theoretischer Grundlagen eines der wichtigsten Ziele unserer Fachhochschulausbildung. Laborübungen gibt es ab dem 1. Semester. Wichtig: Alle Studierenden haben einen garantierten Laborplatz in den State-of-the-Art Mikrobiologie- und Molekularbiologielabors sowie Chemie- und Physiklabors.

Sowohl das Erlernen der Grundfertigkeiten im Labor als auch das Beherrschen der gängigen Standardmethoden aus Forschung, Analytik und Produktion stehen auf dem Programm. Laborübungen finden in medizinischen Grundlagen und Biologie, Analytik, Biotechnologie, Bioprozesstechnologie und Qualitätsmanagement statt.

Das 22-wöchige Berufspraktikum ermöglicht Ihnen darüber hinaus noch weitere praktische Erfahrungen und Einblicke in den Forschungs- und Arbeitsalltag.

Ausgezeichnete Karriereaussichten

Als Absolventin oder Absolvent haben Sie hervorragende Karrieremöglichkeiten in der Pharmaindustrie, bei Technologieunternehmen und in Forschungsinstituten der Krebs- und Stammzellforschung, in der regenerativen Medizin, Arzneimittelentwicklung und Bioverfahrenstechnik.

Ihre Fähigkeiten umfassen die Qualitätskontrolle und Marketing sowie die Entwicklung, Produktion und Zulassung von Biotechnologien für Diagnostik und Therapie. Die perfekte Vorbereitung für zukunftsorientierte Jobs!

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Kompetenzbereiche

Nach Abschluss dieses Bachelor-Studiums verfügen Sie neben fundierten fachlichen und wissenschaftlichen Fähigkeiten auch über sehr gute praktische Fertigkeiten.

Biotechnologie versetzt Sie in die Lage, Probleme zu lösen, auf die in der Medizin bis heute keine befriedigenden Antworten gefunden wurden. Die Entwicklung von Antikörpern für die Arthritis-Therapie oder die neuen Technologien zur Hauttransplantation und Knorpelzüchtung haben die Lebensqualität von Millionen Patientinnen und Patienten weltweit entscheidend verbessert. Dies sind nur die ersten herausragenden Erfolge einer noch jungen Disziplin.

Im Bachelor-Studium entwickeln Sie Ihre Fachkompetenz auf dem Gebiet der Medical and Pharmaceutical Biotechnology. Sie erlernen die Eigenschaften technischer und biologischer Materialien sowie deren Interaktionen, die Grundlagen der Elektrotechnik, Messtechnik in der Bioprozesstechnologie, Steuer- und Regeltechnik sowie des Anlagenbaus und der Prozessentwicklung in der Industrie. Somit sind Sie gerüstet für das praktische Arbeiten in Industrie und Forschung.

Forschung hat in Medical and Pharmaceutical Biotechnology einen sehr hohen Stellenwert. Deswegen vermitteln wir Ihnen die wissenschaftlichen Kompetenzen, um Forschungsprozesse nachvollziehen und erfolgreich mitgestalten zu können.

Während Ihres Studiums erlangen Sie fundierte Kenntnisse des Qualitätsmanagements, hier beispielswiese die gesetzlichen Bestimmungen in der pharmazeutischen Industrie, die Reinraumschulung für die richtige Arbeitsweise im Reinraum und das Reinraum-Monitoring.

Die medizinische und pharmazeutische Biotechnologie ist grundsätzlich ein sehr disziplinenübergreifender Fachbereich. So werden auch Erkenntnisse aus der Mikrobiologie, Biochemie, Molekularbiologie, Genetik, Bioinformatik, den Ingenieurwissenschaften und der Verfahrenstechnik berücksichtigt.

Interdisziplinäres Zusammenarbeiten und Denken wird Sie also auch in Ihrem Arbeitsalltag begleiten und wird daher bereits im Studium stark gefördert.

Karrierewege nach dem Bachelor-Studium Medical and Pharmaceutical Biotechnology

Nach dem Studium haben Sie hervorragende Jobaussichten durch die Ausbildung in enger Abstimmung mit Industrie und Forschung.

Absolventinnen und Absolventen des Studienganges Medical and Pharmaceutical Biotechnology sind aufgrund ihrer interdisziplinären Ausbildung und des einzigartigen Fähigkeitenprofils gefragte Arbeitskräfte.

Nach dem Studium haben Sie die Wahl: Entweder Sie entscheiden sich für den direkten Berufseinstieg oder für ein aufbauendes Master-Studium. Unser Tipp: unser Master-Studium Medical and Pharmaceutical Biotechnology, das perfekt auf die Inhalte des Bachelor-Studiums aufbaut.

Selbstverständlich steht Ihnen nach Ihrem Abschluss auch jedes andere aufbauende Master-Studium im In- oder Ausland offen.

Mögliche Arbeitsbereiche
Biotechnologische Produktion & biotechnologische Prozessentwicklung
Arbeit im biomedizinischen Routinelabor oder im anwendungsorientierten Forschungslabor
Qualitätssicherung von Verfahren und Produkten
Zulassung, Marketing und Vertrieb von Arzneimitteln
Prüfung & Zulassung von biotechnologischen Produkten in Behörden und Dienstleistungseinrichtungen

10 Gründe

Es gibt viele Gründe, warum wir auf unsere Hochschule stolz sind. Finden Sie heraus, was uns besonders macht.

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Studierenden-Stadt Krems

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Studienberatung

Brauchen Sie Hilfe bei der Entscheidung fürs Studium? Unsere Studienberatung berät Sie gerne in einem persönlichen Gespräch.

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Im Fokus: Medical and Pharmaceutical Biotechnology

Klicken Sie sich durch die Videos des Studiengangs.

Lernen Sie unsere Fachhochschule von einer ganz neuen und persönlichen Seite virtuell kennen.

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Info-Veranstaltungen

Bachelor Info Day 2021
Donnerstag
02.12.2021
14:00 - 17:30
Bachelor Info Day 2021
Ein Nachmittag in ganz persönlicher entspannter Atmosphäre mit unseren Studierenden und Studiengangsleiter*innen.
IMC Campus Krems | Trakt G1IMC Campus Krems | Trakt G1
Open House 2022
Samstag
19.02.2022
09:00 - 15:00
Open House 2022
Erhalten Sie den perfekten Einblick in den Studienalltag an der IMC FH Krems und sprechen Sie mit Studierenden und Studiengangsleitungen
IMC Campus Krems | Trakt G1IMC Campus Krems | Trakt G1
Bachelor Info Day 2022
Donnerstag
10.03.2022
14:00 - 17:30
Bachelor Info Day 2022
Ein Nachmittag in ganz persönlicher entspannter Atmosphäre mit unseren Studierenden und Studiengangsleiter*innen.
IMC Campus Krems | Trakt G1IMC Campus Krems | Trakt G1

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Unser Team

Lernen Sie das Kern-Team des Bachelor-Studiengangs Medical and Pharmaceutical Biotechnology kennen.

Prof.(FH) Priv.-Doz. Mag. Dr. Harald Hundsberger
Institutsleitung Biotechnologie / Studiengangsleitung Medical and Pharmaceutical Biotechnology
Institut Biotechnologie
+43 2732 802 521
[email protected]
IMC Campus KremsIMC Campus Trakt G
Heterologe Experssion von Proteinen, Zellkultursysteme, Zellkulturmodelle, Peptidengineering
Produktentwicklung in der Life Science Branche, Projektleitung und Projektmanagement
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Master of Science in Engineering / Vollzeit
Extrazelluläre Vesikel aus dem Hoffa-Fettkörper - ein neuer Ansatz der Knorpelregeneration?
Department of Life Sciences
Testung von rekombinanten polyklonalen Antikörperfragmenten gegen Gluten-Peptide
Projektleitung, Department of Life Sciences
Die Rolle von NFR2 in der Melanomprogression - Einblicke in die Mechanismen von Metastasen
Projektleitung, Department of Life Sciences
Etablierung der molekularen Toxikologie für rasche, frühzeitige sowie sensitive Toxizitätsbestimmungen und Biokompatibilität
Projektleitung, Department of Life Sciences
Entwicklung einer Design-Pipeline für innovative Protein-Protein-Interaktionshemmer
Department of Life Sciences
MEMESA – Metastasierendes Melanom Spezifische Antikörper
Projektleitung, Department of Life Sciences
AdsorbTech: Entwicklung einer neuen Technologieplattform für Peptid-basierte therapeutische Apheresesysteme
Projektleitung, Department of Life Sciences
Entwicklung neuer immunregulierender Peptide und geschlechtsspezifischer organotypischer Zellmodelle für humane Sepsis
Department of Life Sciences
Entwicklung neuer Methoden zur Verbesserung von immuntherapeutischen Verfahren in der Onkologie
Department of Life Sciences
Funktionale Validierung prädiktiver Biomarker für zielgerichtete Krebstherapien
Department of Life Sciences
Etablierung innovativer, vaskulärer Äquivalente zur Entwicklung von Detektionsmodulen für Hochdurchsatz-Verfahren und zur Entwicklung von anti-entzündlichen Peptiden
Projektleitung, Department of Life Sciences
Etablierung innovativer humaner Tumor-Mimetika für das Screening von bioaktiven Wirkstoffen
Department of Life Sciences
Biopharm - Isolation bioaktiver Stoffe aus Cyanobakterien
Projektleitung, Department of Life Sciences
Zellbasierte Testsysteme für bioaktive Substanzen
Projektleitung, Department of Life Sciences
Hundsberger, H., Stierschneider, A., Sarne, V., Ripper, D., Schimon, J., Weitzenböck, H. P., Schild, D., Jacobi, N., Eger, A., Atzler, J., Klein, C. T., & Wiesner, C. (2021): Concentration-Dependent Pro- and Antitumor Activities of Quercetin in Human Melanoma Spheroids: Comparative Analysis of 2D and 3D Cell Culture Models. Molecules (Basel, Switzerland), 26(3): 717.
Doi: https://doi.org/10.3390/molecules26030717
Kinslechner, K., Schütz, B., Pistek, M., Rapolter, P., Weitzenböck, H. P., Hundsberger, H., Mikulits, W., Grillari, J., Röhrl, C., Hengstschläger, M., Stangl, H., & Mikula, M. (2019): Loss of SR-BI Down-Regulates MITF and Suppresses Extracellular Vesicle Release in Human Melanoma. International journal of molecular sciences, 20(5): 1063.
Doi: https://doi.org/10.3390/ijms20051063
Jacobi, N., Seeboeck, R., Hofmann, E., Schweiger, H., Smolinska, V., Mohr, T., Boyer, A., Sommergruber, W., Lechner, P., Pichler-Huebschmann, C., Önder, K., Hundsberger, H., Wiesner, C., & Eger, A. (2017): Organotypic three-dimensional cancer cell cultures mirror drug responses in vivo: lessons learned from the inhibition of EGFR signaling. Oncotarget, 8(64): 107423–107440.
Doi: https://doi.org/10.18632/oncotarget.22475
Hundsberger, H., Önder, K., Schuller-Götzburg, P., Virok, D. P., Herzog, J., & Rid, R. (2017): Assembly and use of high-density recombinant peptide chips for large-scale ligand screening is a practical alternative to synthetic peptide libraries. BMC genomics, 18(1): 450.
Doi: https://doi.org/10.1186/s12864-017-3814-3
Jacobi, N., Smolinska, V., Seeboeck, R., Stierschneider, A., Klein, C., Hofmann, E., Wiesner, C., Mohr, T., Oender, K., Lechner, P., Kaiser, H., Hundsberger, H., Eger, A. (2017): 3D Anti-Cancer drug discovery models: A promising approach for precision medicine. In IMC Fachhochschule Krems GmbH (Hrsg.), Online-Tagungsband FHK Forschungsforum 2017. Krems: FFH.
Hundsberger, H., Koppensteiner, A., Hofmann, E., Ripper, D., Pflüger, M., Stadlmann, V., Klein, C. T., Kreiseder, B., Katzlinger, M., Eger, A., Forster, F., Missbichler, A., & Wiesner, C. (2017): A Screening Approach for Identifying Gliadin Neutralizing Antibodies on Epithelial Intestinal Caco-2 Cells. SLAS discovery : advancing life sciences R & D, 22(8): 1035–1043.
Doi: https://doi.org/10.1177/2472555217697435
Volk, K., Breunig, S. D., Rid, R., Herzog, J., Bräuer, M., Hundsberger, H., Klein, C., Müller, N., & Önder, K. (2017): Structural analysis and interaction studies of acyl-carrier protein (acpP) of Staphylococcus aureus, an extraordinarily thermally stable protein. Biological chemistry, 398(1): 125-133.
Doi: https://doi.org/10.1515/hsz-2016-0185
Schütz, B., Koppensteiner, A., Schörghofer, D., Kinslechner, K., Timelthaler, G., Eferl, R., Hengstschläger, M., Missbichler, A., Hundsberger, H., & Mikula, M. (2016): Generation of metastatic melanoma specific antibodies by affinity purification. Scientific reports, 6: 37253.
Doi: https://doi.org/10.1038/srep37253
Al-Harthy, T., Zoghaib, W. M., Pflüger, M., Schöpel, M., Önder, K., Reitsammer, M., Hundsberger, H., Stoll, R., & Abdel-Jalil, R. (2016): Design, Synthesis, and Cytotoxicity of 5-Fluoro-2-methyl-6-(4-aryl-piperazin-1-yl) Benzoxazoles. Molecules, 21(10): 1290.
Doi: https://doi.org/10.3390/molecules21101290
Al-Harthy, T., Abdel-Jalil, R., Zoghaib, W., Pflüger, M., Hofmann, E., & Hundsberger, H. (2016): Design and synthesis of benzothiazole schiff bases of potential antitumor activity. Heterocycles, 92(7): 1282-1292.
Doi: https://doi.org/10.3987/COM-16-13471
Hofmann, E., Seeboeck, R., Jacobi, N., Obrist, P., Huter, S., Klein, C., Oender, K., Wiesner, C., Hundsberger, H., & Eger, A. (2016): The combinatorial approach of laser-captured microdissection and reverse transcription quantitative polymerase chain reaction accurately determines HER2 status in breast cancer. Biomarker research, 7(4): 8.
Doi: https://doi.org/10.1186/s40364-016-0062-7
Jacobi, N., Smolinska, V., Stierschneider, A., Klein, C., Oender, K., Lechner, P., Kaiser, H., Hundsberger, H., Eger, A. (2016): Development of organotypic cancer models for the identification of individualized cancer therapies. In FH des BFI Wien (Hrsg.), Online-Tagungsband FHK Forschungsforum 2016. Wien: FFH.
Herzog, J., Rid, R., Wagner, M., Hundsberger, H., Eger, A., Bauer, J., & Önder, K. (2015): Whole-transcriptome gene expression profiling in an epidermolysis bullosa simplex Dowling-Meara model keratinocyte cell line uncovered novel, potential therapeutic targets and affected pathways. BMC research notes, 8: 785.
Doi: https://doi.org/10.1186/s13104-015-1783-7
Kreiseder, B., Holper-Schichl, Y. M., Muellauer, B., Jacobi, N., Pretsch, A., Schmid, J. A., de Martin, R., Hundsberger, H., Eger, A., & Wiesner, C. (2015): Alpha-catulin contributes to drug-resistance of melanoma by activating NF-κB and AP-1. PloS one, 10(3): e0119402.
Doi: https://doi.org/10.1371/journal.pone.0119402
Pretsch, A., Nagl, M., Schwendinger, K., Kreiseder, B., Wiederstein, M., Pretsch, D., Genov, M., Hollaus, R., Zinssmeister, D., Debbab, A., Hundsberger, H., Eger, A., Proksch, P., & Wiesner, C. (2014): Antimicrobial and anti-inflammatory activities of endophytic fungi Talaromyces wortmannii extracts against acne-inducing bacteria. PloS one, 9(6): e97929.
Doi: https://doi.org/10.1371/journal.pone.0097929
Rid, R., Hundsberger, H., & Onder, K. (2014): Compound screening and transcriptional profiling in human primary keratinocytes: a brief guideline. Methods in molecular biology, 1195: 99-109.
Doi: https://doi.org/10.1007/7651_2013_50
Kapuścik, A., Hrouzek, P., Kuzma, M., Bártová, S., Novák, P., Jokela, J., Pflüger, M., Eger, A., Hundsberger, H., Kopecký, J. (2013): Novel Aeruginosin-865 from Nostoc sp. as a potent anti-inflammatory agent. Chembiochem : a European journal of chemical biology, 14(17): 2329-2337.
Doi: https://doi.org/10.1002/cbic.201300246
Rid, R., Herzog, J., Maier, R. H., Hundsberger, H., Eger, A., Hintner, H., Bauer, J. W., Onder, K. (2013): Real-time monitoring of relative peptide-protein interaction strengths in the yeast two-hybrid system. Assay and drug development technologies, 11(4): 269-275.
Doi: https://doi.org/10.1089/adt.2012.496
Rid, R., Wagner, M., Maier, C. J., Hundsberger, H., Hintner, H., Bauer, J. W., & Onder, K. (2013): Deciphering the calcitriol-induced transcriptomic response in keratinocytes: presentation of novel target genes. Journal of molecular endocrinology, 50(2): 131–149.
Doi: https://doi.org/10.1530/JME-11-0191
Kreiseder, B., Orel, L., Bujnow, C., Buschek, S., Pflueger, M., Schuett, W., Hundsberger, H., de Martin, R., Wiesner, C. (2013): α‐Catulin downregulates E‐cadherin and promotes melanoma progression and invasion. International journal of cancer, 132(3): 521-530.
Doi: https://doi.org/10.1002/ijc.27698
Pflüger, M., Kapuscik, A., Lucas, R., Koppensteiner, A., Katzlinger, M., Jokela, J., Eger, A., Jacobi, N., Wiesner, C., Hofmann, E., Onder, K., Kopecky, J., Schütt, W., Hundsberger, H. (2013): A combined impedance and AlphaLISA-based approach to identify anti-inflammatory and barrier-protective compounds in human endothelium. Journal of biomolecular screening, 18(1): 67-74.
Doi: https://doi.org/10.1177/1087057112458316
Khare, V., Lyakhovich, A., Dammann, K., Lang, M., Borgmann, M., Tichy, B., Pospisilova, S., Luciani, G., Campregher, C., Evstatiev, R., Pflueger, M., Hundsberger, H., & Gasche, C. (2013): Mesalamine modulates intercellular adhesion through inhibition of p-21 activated kinase-1. Biochemical Pharmacology, 85(2): 234-244.
Doi: https://doi.org/10.1016/j.bcp.2012.10.026
Maier, C., Maier, R., Rid, R., Trost, A., Hundsberger, H., Eger, A., Hintner, H., Bauer, J., Onder, K. (2012): PIM-1 kinase interacts with the DNA binding domain of the vitamin D receptor: a further kinase implicated in 1,25-(OH)2D3 signaling. BMC molecular biology, 13: 18.
Doi: https://doi.org/10.1186/1471-2199-13-18
Amatschek, S., Lucas, R., Eger, A., Pflueger, M., Hundsberger, H., Knoll, C., Grosse-Kracht, S., Schuett, W., Koszik, F., Maurer, D., Wiesner, C. (2011): CXCL9 induces chemotaxis, chemorepulsion and endothelial barrier disruption through CXCR3-mediated activation of melanoma cells. British journal of cancer, 104(3): 469-479.
Doi: https://doi.org/10.1038/sj.bjc.6606056
Hundsberger, H., Verin, A., Wiesner, C., Pflüger, M., Dulebo, A., Schütt, W., Lasters, I., Männel, D., Wendel, A., Lucas, R. (2008): TNF: a moonlighting protein at the interface between cancer and infection. Frontiers in Bioscience, 13: 5374-86.
Doi: https://doi.org/10.2741/3087
Hundsberger, H., Verin, A., Wiesner, C., Pflüger, M., Dulebo, A., Schütt, W., Lasters, I., Männel, D. N., Wendel, A., & Lucas, R. (2008): TNF: a moonlighting protein at the interface between cancer and infection. Frontiers in bioscience : a journal and virtual library, 13: 5374–5386.
Doi: https://doi.org/10.2741/3087
Wiesner, C., Pflueger, M., Kopecky, J., Stys, D., Entler, B., Lucas, R., Hundsberger, H., Schuett, W. (2008): Implementation of ECIS technology for the characterization of potential therapeutic drugs that promote wound-healing. GMS Krankenhaushygiene interdisziplinar, 3(1).
Wiesner, C., Pflüger, M., Kopecky, J., Stys, D., Entler, B., Lucas, R., Hundsberger, H., Schütt, W. (2008): Implementation of ECIS technology for the characterization of potential therapeutic drugs that promote wound-healing. GMS Krankenhaushygiene Interdisziplinär, 3(1): Doc05.
Wiesner, C., Lucas, R., Pflueger, M., Kleber, C., Kopecky, J., Stys, D., Entler, B., Hundsberger, H., Atzler, J., Hrouzek, P., Lukesova, A., Schuett, W., (2007): Endothelial Cell-Based Methods for the Detection of Cyanobacterial Anti- Inflammatory and Wound-Healing Promoting Metabolites. Drug Metabolism Letters, 1(4): 254-260.
Doi: https://doi.org/10.2174/187231207783221385
Lucas, R., Hundsberger, H., Pflueger, M., Fischer, B., Morel, D., Braun, C., Wendel, A., Chakraborty, T., Schuett, W., Wiesner, C., Hamacher, J. (2007): The Tumor Necrosis Factor-Derived TIP Peptide: A Potential Anti-Edema Drug. Letters in Drug Design & Discovery, 4(5): 336-340.
Doi: https://doi.org/10.2174%2F157018007780867816
Prof.(FH) Priv.-Doz. Mag. Dr. Harald Hundsberger
Institutsleitung Biotechnologie / Studiengangsleitung Medical and Pharmaceutical Biotechnology
Institutsleitung Biotechnologie / Studiengangsleitung Medical and Pharmaceutical Biotechnology
Prof.(FH) Priv.-Doz. Mag. Dr. Harald Hundsberger
Kernkompetenzen
- Heterologe Experssion von Proteinen, Zellkultursysteme, Zellkulturmodelle, Peptidengineering
- Produktentwicklung in der Life Science Branche, Projektleitung und Projektmanagement

Mag. Dr. Peter Allacher
Operative Leitung / Institute Krems Bioanalytics
Institute Krems Bioanalytics
+43 2732 802 281
[email protected]
IMC TFZIMC TFZ Haupthaus
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Lubich, C., Allacher, P., de la Rosa, M., Bauer, A., Prenninger, T., Horling, F. M., Siekmann, J., Oldenburg, J., Scheiflinger, F., & Reipert, B. M. (2016): The Mystery of Antibodies Against Polyethylene Glycol (PEG) - What do we Know?. Pharmaceutical research, 33(9): 2239-49.
Doi: https://doi.org/10.1007/s11095-016-1961-x
Jaki, T., Allacher, P., & Horling, F. (2016): A false sense of security? Can tiered approach be trusted to accurately classify immunogenicity samples?. Journal of pharmaceutical and biomedical analysis, 128: 166-73.
Doi: https://doi.org/10.1016/j.jpba.2016.05.031
Hofbauer, C.J., Whelan,S.F.J., Hirschler, M., Allacher, P., Horling, F.M., Lawo, J.-P., Oldenburg, J., Tiede, A., Male, C., Windyga, J., Greinacher, A., Knöbl, P.N., Schrenk, G., Koehn, J., Scheiflinger, F., Reipert, B.M. (2015): Affinity of FVIII-specific antibodies reveals major differences between neutralizing and nonneutralizing antibodies in humans. Blood, 125(7): 1180-1188.
Doi: https://doi.org/10.1182/blood-2014-09-598268
Jaki, T., Lawo, J.-P., Wolfsegger, M.J., Allacher, P., Horling, F. (2014): A comparison of methods for classifying samples as truly specific with confirmatory immunoassays. Journal of pharmaceutical and biomedical analysis, 88: 27-35.
Doi: https://doi.org/10.1016/j.jpba.2013.08.013
Whelan, S. F., Hofbauer, C. J., Horling, F. M., Allacher, P., Wolfsegger, M. J., Oldenburg, J., Male, C., Windyga, J., Tiede, A., Schwarz, H. P., Scheiflinger, F., & Reipert, B. M. (2013): Distinct characteristics of antibody responses against factor VIII in healthy individuals and in different cohorts of hemophilia A patients. Blood, 121(6): 1039-1048.
Doi: https://doi.org/10.1182/blood-2012-07-444877
Pordes, A. G., Baumgartner, C. K., Allacher, P., Ahmad, R. U., Weiller, M., Schiviz, A. N., Schwarz, H. P., & Reipert, B. M. (2011): T cell-independent restimulation of FVIII-specific murine memory B cells is facilitated by dendritic cells together with toll-like receptor 7 agonist. Blood, 118(11): 3154–3162.
Doi: https://doi.org/10.1182/blood-2011-02-336198
Jaki, T., Lawo, J.-P., Wolfsegger, M.J., Singer, J., Allacher, P., Horling, F. (2011): A formal comparison of different methods for establishing cut points to distinguish positive and negative samples in immunoassays. Journal of pharmaceutical and biomedical analysis, 55(5): 1148-1156.
Doi: https://doi.org/10.1016/j.jpba.2011.04.006
Allacher, P., Baumgartner, C. K., Pordes, A. G., Ahmad, R. U., Schwarz, H. P., & Reipert, B. M. (2011): Stimulation and inhibition of FVIII-specific memory B-cell responses by CpG-B (ODN 1826), a ligand for Toll-like receptor 9. Blood, 117(1): 259-267.
Doi: https://doi.org/10.1182/blood-2010-06-289009
Reipert, B. M., Allacher, P., Hausl, C., Pordes, A. G., Ahmad, R. U., Lang, I., Ilas, J., Windyga, J., Klukowska, A., Muchitsch, E. M., & Schwarz, H. P. (2010): Modulation of factor VIII-specific memory B cells. Haemophilia, 16(102): 25-34.
Doi: https://doi.org/10.1111/j.1365-2516.2008.01962.x
Mag. Dr. Peter Allacher
Operative Leitung / Institute Krems Bioanalytics
Prof.(FH) Priv. Doz. Mag. Dr. Andreas Eger
Institutsleitung Institute Krems Bioanalytics / Professor Department of Life Sciences
Institute Krems Bioanalytics
+43 2732 802 369
[email protected]
IMC Campus KremsIMC Campus Trakt G
Wirkstoffentwicklung
Organotypische Krankheitsmodelle
Bioanalytik und Biomarker
Medical and Pharmaceutical Biotechnology
Master of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Stoffwechsel-Plasma-Analyse bei metabolischem Syndrom und Tumorkachexie
Projektleitung, Department of Life Sciences
DNA Methylierung im Lungenkrebs und ihre geschlechtsspezifische Auswirkung auf die Effizienz epigenetischer Therapien
Department of Life Sciences
Entwicklung von therapeutischen Peptiden für Krebs- und regenerative Medizin
Projektleitung, Department of Life Sciences
Etablierung der molekularen Toxikologie für rasche, frühzeitige sowie sensitive Toxizitätsbestimmungen und Biokompatibilität
Department of Life Sciences
Entwicklung komplexer extrakorporaler Karzinommodelle für die Identifikation personalisierter Krebstherapien
Projektleitung, Department of Life Sciences
AdsorbTech: Entwicklung einer neuen Technologieplattform für Peptid-basierte therapeutische Apheresesysteme
Department of Life Sciences
Entwicklung neuer immunregulierender Peptide und geschlechtsspezifischer organotypischer Zellmodelle für humane Sepsis
Department of Life Sciences
Entwicklung neuer Methoden zur Verbesserung von immuntherapeutischen Verfahren in der Onkologie
Projektleitung, Department of Life Sciences
Funktionale Validierung prädiktiver Biomarker für zielgerichtete Krebstherapien
Projektleitung, Department of Life Sciences
Etablierung innovativer humaner Tumor-Mimetika für das Screening von bioaktiven Wirkstoffen
Projektleitung, Department of Life Sciences
Hundsberger, H., Stierschneider, A., Sarne, V., Ripper, D., Schimon, J., Weitzenböck, H. P., Schild, D., Jacobi, N., Eger, A., Atzler, J., Klein, C. T., & Wiesner, C. (2021): Concentration-Dependent Pro- and Antitumor Activities of Quercetin in Human Melanoma Spheroids: Comparative Analysis of 2D and 3D Cell Culture Models. Molecules (Basel, Switzerland), 26(3): 717.
Doi: https://doi.org/10.3390/molecules26030717
Jacobi, N., Seeboeck, R., Hofmann, E., Schweiger, H., Smolinska, V., Mohr, T., Boyer, A., Sommergruber, W., Lechner, P., Pichler-Huebschmann, C., Önder, K., Hundsberger, H., Wiesner, C., & Eger, A. (2017): Organotypic three-dimensional cancer cell cultures mirror drug responses in vivo: lessons learned from the inhibition of EGFR signaling. Oncotarget, 8(64): 107423–107440.
Doi: https://doi.org/10.18632/oncotarget.22475
Jacobi, N., Smolinska, V., Seeboeck, R., Stierschneider, A., Klein, C., Hofmann, E., Wiesner, C., Mohr, T., Oender, K., Lechner, P., Kaiser, H., Hundsberger, H., Eger, A. (2017): 3D Anti-Cancer drug discovery models: A promising approach for precision medicine. In IMC Fachhochschule Krems GmbH (Hrsg.), Online-Tagungsband FHK Forschungsforum 2017. Krems: FFH.
Jacobi, N., Seeboeck, R., Hofmann, E., & Eger, A. (2017): ErbB Family Signalling: A Paradigm for Oncogene Addiction and Personalized Oncology. Cancers, 9(4): 33.
Doi: https://doi.org/10.3390/cancers9040033
Hundsberger, H., Koppensteiner, A., Hofmann, E., Ripper, D., Pflüger, M., Stadlmann, V., Klein, C. T., Kreiseder, B., Katzlinger, M., Eger, A., Forster, F., Missbichler, A., & Wiesner, C. (2017): A Screening Approach for Identifying Gliadin Neutralizing Antibodies on Epithelial Intestinal Caco-2 Cells. SLAS discovery : advancing life sciences R & D, 22(8): 1035–1043.
Doi: https://doi.org/10.1177/2472555217697435
Hofmann, E., Seeboeck, R., Jacobi, N., Obrist, P., Huter, S., Klein, C., Oender, K., Wiesner, C., Hundsberger, H., & Eger, A. (2016): The combinatorial approach of laser-captured microdissection and reverse transcription quantitative polymerase chain reaction accurately determines HER2 status in breast cancer. Biomarker research, 7(4): 8.
Doi: https://doi.org/10.1186/s40364-016-0062-7
Jacobi, N., Smolinska, V., Stierschneider, A., Klein, C., Oender, K., Lechner, P., Kaiser, H., Hundsberger, H., Eger, A. (2016): Development of organotypic cancer models for the identification of individualized cancer therapies. In FH des BFI Wien (Hrsg.), Online-Tagungsband FHK Forschungsforum 2016. Wien: FFH.
Herzog, J., Rid, R., Wagner, M., Hundsberger, H., Eger, A., Bauer, J., & Önder, K. (2015): Whole-transcriptome gene expression profiling in an epidermolysis bullosa simplex Dowling-Meara model keratinocyte cell line uncovered novel, potential therapeutic targets and affected pathways. BMC research notes, 8: 785.
Doi: https://doi.org/10.1186/s13104-015-1783-7
Kreiseder, B., Holper-Schichl, Y. M., Muellauer, B., Jacobi, N., Pretsch, A., Schmid, J. A., de Martin, R., Hundsberger, H., Eger, A., & Wiesner, C. (2015): Alpha-catulin contributes to drug-resistance of melanoma by activating NF-κB and AP-1. PloS one, 10(3): e0119402.
Doi: https://doi.org/10.1371/journal.pone.0119402
Bakiri, L., Macho-Maschler, S., Custic, I., Niemiec, J., Guío-Carrión, A., Hasenfuss, S. C., Eger, A., Müller, M., Beug, H., & Wagner, E. F. (2015): Fra-1/AP-1 induces EMT in mammary epithelial cells by modulating Zeb1/2 and TGFβ expression. Cell death and differentiation, 22(2): 336–350.
Doi: https://doi.org/10.1038/cdd.2014.157
Spilka, R., Ernst, C., Bergler, H., Rainer, J., Flechsig, S., Vogetseder, A., Lederer, E., Benesch, M., Brunner, A., Geley, S., Eger, A., Bachmann, F., Doppler, W., Obrist, P., & Haybaeck, J. (2014): eIF3a is over-expressed in urinary bladder cancer and influences its phenotype independent of translation initiation. Cellular oncology (Dordrecht), 37(4): 253–267.
Doi: https://doi.org/10.1007/s13402-014-0181-9
Pretsch, A., Nagl, M., Schwendinger, K., Kreiseder, B., Wiederstein, M., Pretsch, D., Genov, M., Hollaus, R., Zinssmeister, D., Debbab, A., Hundsberger, H., Eger, A., Proksch, P., & Wiesner, C. (2014): Antimicrobial and anti-inflammatory activities of endophytic fungi Talaromyces wortmannii extracts against acne-inducing bacteria. PloS one, 9(6): e97929.
Doi: https://doi.org/10.1371/journal.pone.0097929
Kapuścik, A., Hrouzek, P., Kuzma, M., Bártová, S., Novák, P., Jokela, J., Pflüger, M., Eger, A., Hundsberger, H., Kopecký, J. (2013): Novel Aeruginosin-865 from Nostoc sp. as a potent anti-inflammatory agent. Chembiochem : a European journal of chemical biology, 14(17): 2329-2337.
Doi: https://doi.org/10.1002/cbic.201300246
Rid, R., Herzog, J., Maier, R. H., Hundsberger, H., Eger, A., Hintner, H., Bauer, J. W., Onder, K. (2013): Real-time monitoring of relative peptide-protein interaction strengths in the yeast two-hybrid system. Assay and drug development technologies, 11(4): 269-275.
Doi: https://doi.org/10.1089/adt.2012.496
Pflüger, M., Kapuscik, A., Lucas, R., Koppensteiner, A., Katzlinger, M., Jokela, J., Eger, A., Jacobi, N., Wiesner, C., Hofmann, E., Onder, K., Kopecky, J., Schütt, W., Hundsberger, H. (2013): A combined impedance and AlphaLISA-based approach to identify anti-inflammatory and barrier-protective compounds in human endothelium. Journal of biomolecular screening, 18(1): 67-74.
Doi: https://doi.org/10.1177/1087057112458316
Imhof, M., Karas, I., Gomez, I., Eger, A., & Imhof, M. (2013): Interaction of tumor cells with the immune system: implications for dendritic cell therapy and cancer progression. Drug discovery today, 18(1-2): 35-42.
Doi: https://doi.org/10.1016/j.drudis.2012.07.010
Maier, C., Maier, R., Rid, R., Trost, A., Hundsberger, H., Eger, A., Hintner, H., Bauer, J., Onder, K. (2012): PIM-1 kinase interacts with the DNA binding domain of the vitamin D receptor: a further kinase implicated in 1,25-(OH)2D3 signaling. BMC molecular biology, 13: 18.
Doi: https://doi.org/10.1186/1471-2199-13-18
Vonach, C., Viola, K., Giessrigl, B., Huttary, N., Raab, I., Kalt, R., Krieger, S., Vo, T. P., Madlener, S., Bauer, S., Marian, B., Hämmerle, M., Kretschy, N., Teichmann, M., Hantusch, B., Stary, S., Unger, C., Seelinger, M., Eger, A., Mader, R., Jäger, W., Schmidt, W., Grusch, M., Dolznig, H., Mikulits, W., Krupitza, G. (2011): NF-κB mediates the 12(S)-HETE-induced endothelial to mesenchymal transition of lymphendothelial cells during the intravasation of breast carcinoma cells. British journal of cancer, 105(2): 263-271.
Doi: https://doi.org/10.1038/bjc.2011.194
Amatschek, S., Lucas, R., Eger, A., Pflueger, M., Hundsberger, H., Knoll, C., Grosse-Kracht, S., Schuett, W., Koszik, F., Maurer, D., Wiesner, C. (2011): CXCL9 induces chemotaxis, chemorepulsion and endothelial barrier disruption through CXCR3-mediated activation of melanoma cells. British journal of cancer, 104(3): 469-479.
Doi: https://doi.org/10.1038/sj.bjc.6606056
Spaderna, S., Schmalhofer, O., Wahlbuhl, M., Dimmler, A., Bauer, K., Sultan, A., Hlubek, F., Jung, A., Strand, D., Eger, A., Kirchner, T., Behrens, J., & Brabletz, T. (2008): The transcriptional repressor ZEB1 promotes metastasis and loss of cell polarity in cancer. Cancer research, 68(2): 537–544.
Doi: https://doi.org/10.1158/0008-5472.CAN-07-5682
Mikula M., Lahsnig C., Fischer A. N. M., Proell V., Huber H, Fuchs E., Eger A., Beug H. and Mikulits W. (2007): Epithelial plasticity of hepatocytes during liver tumor progression. Stem cells and their potential for clinical application. NATO Science for Peace and Security. Series/NATO Science Foundation. Springer Netherland, Edition 1.
Aigner, K., Dampier, B., Descovich, L., Mikula, M., Sultan, A., Schreiber, M., Mikulits, W., Brabletz, T., Strand, D., Obrist, P., Sommergruber, W., Schweifer, N., Wernitznig, A., Beug, H., Foisner, R., & Eger, A. (2007): The transcription factor ZEB1 (deltaEF1) promotes tumour cell dedifferentiation by repressing master regulators of epithelial polarity. Oncogene, 26(49): 6979–6988.
Doi: https://doi.org/10.1038/sj.onc.1210508
Aigner, K., Descovich, L., Mikula, M., Sultan, A., Dampier, B., Bonné, S., van Roy, F., Mikulits, W., Schreiber, M., Brabletz, T., Sommergruber, W., Schweifer, N., Wernitznig, A., Beug, H., Foisner, R., & Eger, A. (2007): The transcription factor ZEB1 (deltaEF1) represses Plakophilin 3 during human cancer progression. FEBS letters, 581(8): 1617-24.
Doi: https://doi.org/10.1016/j.febslet.2007.03.026
Pacher, M., Seewald, M. J., Mikula, M., Oehler, S., Mogg, M., Vinatzer, U., Eger, A., Schweifer, N., Varecka, R., Sommergruber, W., Mikulits, W., & Schreiber, M. (2007): Impact of constitutive IGF1/IGF2 stimulation on the transcriptional program of human breast cancer cells. Carcinogenesis, 28(1): 49-59.
Doi: https://doi.org/10.1093/carcin/bgl091
Spaderna, S., Schmalhofer, O., Hlubek, F., Berx, G., Eger, A., Merkel, S., Jung, A., Kirchner, T., & Brabletz, T. (2006): A transient, EMT-linked loss of basement membranes indicates metastasis and poor survival in colorectal cancer. Gastroenterology, 131(3): 830–840.
Doi: https://doi.org/10.1053/j.gastro.2006.06.016
Stary, M., Pasteiner, W., Summer, A., Hrdina, A., Eger, A., & Weitzer, G. (2005): Parietal endoderm secreted SPARC promotes early cardiomyogenesis in vitro. Experimental cell research, 310(2): 331-43.
Doi: https://doi.org/10.1016/j.yexcr.2005.07.013
Eger, A., Mikulits, W. (2005): Models of Epithelial to Mesenchymal Transition. Drug Discovery Today: Disease Models, 2(1): 57-63.
Doi: https://doi.org/10.1016/j.ddmod.2005.04.001
Eger, A., Aigner, K., Sonderegger, S., Dampier, B., Oehler, S., Schreiber, M., Berx, G., Cano, A., Beug, H., & Foisner, R. (2005): DeltaEF1 is a transcriptional repressor of E-cadherin and regulates epithelial plasticity in breast cancer cells. Oncogene, 24(14): 2375-85.
Doi: https://doi.org/10.1038/sj.onc.1208429
Eger, A., Stockinger, A., Park, J., Langkopf, E., Mikula, M., Gotzmann, J., Mikulits, W., Beug, H., & Foisner, R. (2004): β-catenin and TGFβ signalling cooperate to maintain a mesenchymal phenotype after FosER-induced epithelial to mesenchymal transition. Oncogene, 23(15): 2672-2680.
Doi: https://doi.org/10.1038/sj.onc.1207416
Gotzmann, J., Mikula, M., Eger, A., Schulte-Hermann, R., Foisner, R., Beug, H., & Mikulits, W. (2004): Molecular aspects of epithelial cell plasticity: implications for local tumor invasion and metastasis. Mutation research, 566(1): 9–20.
Doi: https://doi.org/10.1016/s1383-5742(03)00033-4
Stockinger, A., Eger, A., Wolf, J., Beug, H., & Foisner, R. (2001): E-cadherin regulates cell growth by modulating proliferation-dependent beta-catenin transcriptional activity. The Journal of cell biology, 154(6): 1185–1196.
Doi: https://doi.org/10.1083/jcb.200104036
Eger A. and Foisner R. (2000): Dynamic and cross talk of junctional proteins: a molecular basis for the regulation of cell adhesion and epithelial polarity. Protoplasma, 211(3-4): 125-133.
Eger, A., Stockinger, A., Schaffhauser, B., Beug, H., & Foisner, R. (2000): Epithelial mesenchymal transition by c-Fos estrogen receptor activation involves nuclear translocation of beta-catenin and upregulation of beta-catenin/lymphoid enhancer binding factor-1 transcriptional activity. The Journal of cell biology, 148(1): 173-188.
Doi: https://doi.org/10.1083/jcb.148.1.173
Gotzmann, J., Eger, A., Meissner, M., Grimm, R., Gerner, C., Sauermann, G., & Foisner, R. (1997): Two-dimensional electrophoresis reveals a nuclear matrix-associated nucleolin complex of basic isoelectric point. Electrophoresis, 18(14): 2645–2653.
Doi: https://doi.org/10.1002/elps.1150181421
Eger, A., Stockinger, A., Wiche, G., & Foisner, R. (1997): Polarisation-dependent association of plectin with desmoplakin and the lateral submembrane skeleton in MDCK cells. Journal of cell science, 110: 1307-1316.
Prof.(FH) Priv. Doz. Mag. Dr. Andreas Eger
Institutsleitung Institute Krems Bioanalytics / Professor Department...
Prof.(FH) Mag. Dr. Christoph Wiesner
Professor Department of Life Sciences
Institut Biotechnologie
+43 2732 802 276
[email protected]
IMC Campus KremsIMC Campus Trakt G
Zell- und Molekularbiologie
Wirkstoff Screening
Projekt management
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Master of Science in Engineering / Vollzeit
Entwicklung einer optogenetisch kontrollierbaren MSC-Zelllinie für die präzise Regulation immunmodulatorischer Faktoren
Projektleitung, Department of Life Sciences
Biomarker-basierte therapeutische Prävention von Knochenmetastasen beim Mammakarzinom: die phathophysiologische Rolle der endostalen Nische
Projektleitung, Department of Life Sciences
Entwicklung leistungsfähiger Diagnostikverfahren und neuer Therapieansätze in Inflammation und Sepsis
Projektleitung, Department of Life Sciences
Nachhaltiges biologisches Recycling von umweltbedenklichen Stoffen (Rare Earth Elements) aus Elektronikabfall und Abwässern
Department of Life Sciences
Testung von rekombinanten polyklonalen Antikörperfragmenten gegen Gluten-Peptide
Department of Life Sciences
Zellbasierte Testsysteme für bioaktive Substanzen
Department of Life Sciences
Pretsch, A., Nagl, M., Wiesner, C., Hollaus, R., Genov, M. (2021): Polyguanidine polymers and methods of use thereof (US11013760B2). United States Patent Office.
Hundsberger, H., Stierschneider, A., Sarne, V., Ripper, D., Schimon, J., Weitzenböck, H. P., Schild, D., Jacobi, N., Eger, A., Atzler, J., Klein, C. T., & Wiesner, C. (2021): Concentration-Dependent Pro- and Antitumor Activities of Quercetin in Human Melanoma Spheroids: Comparative Analysis of 2D and 3D Cell Culture Models. Molecules (Basel, Switzerland), 26(3): 717.
Doi: https://doi.org/10.3390/molecules26030717
Sarne, V., Huter, S., Braunmueller, S., Rakob, L., Jacobi, N., Kitzwögerer, M., Wiesner, C., Obrist, P., & Seeboeck, R. (2020): Promoter Methylation of Selected Genes in Non-Small-Cell Lung Cancer Patients and Cell Lines. International journal of molecular sciences, 21(13): 4595.
Doi: https://doi.org/10.3390/ijms21134595
Pretsch, A., Nagl, M., Wiesner, C., Hollaus, R., Genov, M. (2019): Method for producing polyguanidines (US10335431B2). United States Patent Office.
Jacobi, N., Seeboeck, R., Hofmann, E., Schweiger, H., Smolinska, V., Mohr, T., Boyer, A., Sommergruber, W., Lechner, P., Pichler-Huebschmann, C., Önder, K., Hundsberger, H., Wiesner, C., & Eger, A. (2017): Organotypic three-dimensional cancer cell cultures mirror drug responses in vivo: lessons learned from the inhibition of EGFR signaling. Oncotarget, 8(64): 107423–107440.
Doi: https://doi.org/10.18632/oncotarget.22475
Jacobi, N., Smolinska, V., Seeboeck, R., Stierschneider, A., Klein, C., Hofmann, E., Wiesner, C., Mohr, T., Oender, K., Lechner, P., Kaiser, H., Hundsberger, H., Eger, A. (2017): 3D Anti-Cancer drug discovery models: A promising approach for precision medicine. In IMC Fachhochschule Krems GmbH (Hrsg.), Online-Tagungsband FHK Forschungsforum 2017. Krems: FFH.
Hundsberger, H., Koppensteiner, A., Hofmann, E., Ripper, D., Pflüger, M., Stadlmann, V., Klein, C. T., Kreiseder, B., Katzlinger, M., Eger, A., Forster, F., Missbichler, A., & Wiesner, C. (2017): A Screening Approach for Identifying Gliadin Neutralizing Antibodies on Epithelial Intestinal Caco-2 Cells. SLAS discovery : advancing life sciences R & D, 22(8): 1035–1043.
Doi: https://doi.org/10.1177/2472555217697435
Pretsch, A., Nagl, M., Wiesner, C., Burgmann, H. (2017): Bioactive polymers (US9567294B2). United States Patent Office.
Genov, M., Kreiseder, B., Nagl, M., Wiesner, C. et al. (2016): Tetrahydroanthraquinone Derivative (±)-4-Deoxyaustrocortilutein Induces Cell Cycle Arrest and Apoptosis in Melanoma Cells via Upregulation of p21 and p53 and Downregulation of NF-kappaB. Journal of Cancer, 7(5): 555.
Doi: https://doi:10.7150/jca.13614
Preisitsch, M., Niedermeyer, T., Heiden, SE., Neidhardt, I., Kumpfmueller, J., Wurster, M., Harmrolfs, K., Wiesner, C., Enke, H., Mueller, R., Mundt, S. (2016): Cylindrofridins A–C, Linear Cylindrocyclophane-Related Alkylresorcinols from the Cyanobacterium Cylindrospermum stagnale. Journal of natural products, 79(1): 106-115.
Doi: https://doi.org/10.1021/acs.jnatprod.5b00768
Preisitsch, M., Heiden, SE., Beerbaum, M., Niedermeyer, T., Schneefeld, M., Herrmann, J., Kumpfmueller, J., Thuermer, A., Neidhardt, I., Wiesner, C., Daniel, R., Mueller, R., Bange, FC., Schmieder, P., Schweder, T., Mundt, S. (2016): Effects of halide ions on the carbamidocyclophane biosynthesis in Nostoc sp. CAVN2. Marine drugs, 14(1): 21.
Doi: https://doi.org/10.3390/md14010021
Preisitsch, M., Harmrolfs, K., Pham, HT., Heidern, SE., Fuessl, A., Wiesner, C., Pretsch, A., Switecka-Hagenbruch, M., Niedermeyer, TH., Mueller, R., Mundt, S. (2015): Anti-MRSA-acting carbamidocyclophanes H-L from the Vietnamese cyanobacterium Nostoc sp. CAVN2. The Journal of antibiotics, 68(9): 600-600.
Doi: https://doi.org/10.1038/ja.2015.79
Kreiseder, B., Holper-Schichl, Y. M., Muellauer, B., Jacobi, N., Pretsch, A., Schmid, J. A., de Martin, R., Hundsberger, H., Eger, A., & Wiesner, C. (2015): Alpha-catulin contributes to drug-resistance of melanoma by activating NF-κB and AP-1. PloS one, 10(3): e0119402.
Doi: https://doi.org/10.1371/journal.pone.0119402
Preisitsch, M., Harmrolfs, K., Pham, H., Heiden, SE., Fuessel, A., Wiesner, C., Pretsch, A., et al. (2015): Anti-MRSA-acting carbamidocyclophanes H–L from the Vietnamese cyanobacterium Nostoc sp. CAVN2. The Journal of antibiotics, 68(3): 165-177.
Doi: https://doi.org/10.1038/ja.2014.118
Pretsch, A., Nagl, M., Schwendinger, K., Kreiseder, B., Wiederstein, M., Pretsch, D., Genov, M., Hollaus, R., Zinssmeister, D., Debbab, A., Hundsberger, H., Eger, A., Proksch, P., & Wiesner, C. (2014): Antimicrobial and anti-inflammatory activities of endophytic fungi Talaromyces wortmannii extracts against acne-inducing bacteria. PloS one, 9(6): e97929.
Doi: https://doi.org/10.1371/journal.pone.0097929
Kreiseder, B., Orel, L., Bujnow, C., Buschek, S., Pflueger, M., Schuett, W., Hundsberger, H., de Martin, R., Wiesner, C. (2013): α‐Catulin downregulates E‐cadherin and promotes melanoma progression and invasion. International journal of cancer, 132(3): 521-530.
Doi: https://doi.org/10.1002/ijc.27698
Pflüger, M., Kapuscik, A., Lucas, R., Koppensteiner, A., Katzlinger, M., Jokela, J., Eger, A., Jacobi, N., Wiesner, C., Hofmann, E., Onder, K., Kopecky, J., Schütt, W., Hundsberger, H. (2013): A combined impedance and AlphaLISA-based approach to identify anti-inflammatory and barrier-protective compounds in human endothelium. Journal of biomolecular screening, 18(1): 67-74.
Doi: https://doi.org/10.1177/1087057112458316
Amatschek, S., Lucas, R., Eger, A., Pflueger, M., Hundsberger, H., Knoll, C., Grosse-Kracht, S., Schuett, W., Koszik, F., Maurer, D., Wiesner, C. (2011): CXCL9 induces chemotaxis, chemorepulsion and endothelial barrier disruption through CXCR3-mediated activation of melanoma cells. British journal of cancer, 104(3): 469-479.
Doi: https://doi.org/10.1038/sj.bjc.6606056
Hundsberger, H., Verin, A., Wiesner, C., Pflüger, M., Dulebo, A., Schütt, W., Lasters, I., Männel, D., Wendel, A., Lucas, R. (2008): TNF: a moonlighting protein at the interface between cancer and infection. Frontiers in Bioscience, 13: 5374-86.
Doi: https://doi.org/10.2741/3087
Hundsberger, H., Verin, A., Wiesner, C., Pflüger, M., Dulebo, A., Schütt, W., Lasters, I., Männel, D. N., Wendel, A., & Lucas, R. (2008): TNF: a moonlighting protein at the interface between cancer and infection. Frontiers in bioscience : a journal and virtual library, 13: 5374–5386.
Doi: https://doi.org/10.2741/3087
Wiesner, C., Pflueger, M., Kopecky, J., Stys, D., Entler, B., Lucas, R., Hundsberger, H., Schuett, W. (2008): Implementation of ECIS technology for the characterization of potential therapeutic drugs that promote wound-healing. GMS Krankenhaushygiene interdisziplinar, 3(1).
Wiesner, C., Pflüger, M., Kopecky, J., Stys, D., Entler, B., Lucas, R., Hundsberger, H., Schütt, W. (2008): Implementation of ECIS technology for the characterization of potential therapeutic drugs that promote wound-healing. GMS Krankenhaushygiene Interdisziplinär, 3(1): Doc05.
Wiesner, C., Winsauer, G., Resch, U. et al. (2008): α-Catulin, a Rho signalling component, can regulate NF-κB through binding to IKK-β, and confers resistance to apoptosis. Oncogene , 27: 2159–2169.
Doi: https://doi.org/10.1038/sj.onc.1210863
Wiesner, C., Lucas, R., Pflueger, M., Kleber, C., Kopecky, J., Stys, D., Entler, B., Hundsberger, H., Atzler, J., Hrouzek, P., Lukesova, A., Schuett, W., (2007): Endothelial Cell-Based Methods for the Detection of Cyanobacterial Anti- Inflammatory and Wound-Healing Promoting Metabolites. Drug Metabolism Letters, 1(4): 254-260.
Doi: https://doi.org/10.2174/187231207783221385
Winter, D., Moser, J., Kriehuber, E., Wiesner, C., Knobler, R., Trautinger, F., Bombosi, P., Stingl, G., Petzelbauer, P., Rot, A., & Maurer, D. (2007): Down-modulation of CXCR3 surface expression and function in CD8+ T cells from cutaneous T cell lymphoma patients. Journal of immunology, 179(6): 4272-4282.
Doi: https://doi.org/10.4049/jimmunol.179.6.4272
Lucas, R., Hundsberger, H., Pflueger, M., Fischer, B., Morel, D., Braun, C., Wendel, A., Chakraborty, T., Schuett, W., Wiesner, C., Hamacher, J. (2007): The Tumor Necrosis Factor-Derived TIP Peptide: A Potential Anti-Edema Drug. Letters in Drug Design & Discovery, 4(5): 336-340.
Doi: https://doi.org/10.2174%2F157018007780867816
Hofer-Warbinek, R., Schmid, J.A., Mayer, H., Winsauer, G., Orel, L., Mueller, B., Wiesner, C., Binder, B.R., de Martin, R. (2004): A highly conserved proapoptotic gene, IKIP, located next to the APAF1 gene locus, is regulated by p53. Cell Death & Differentiation, 11(12): 1317 - 1325.
Doi: https://doi.org/10.1038%2Fsj.cdd.4401502
Wiesner, C., Hoeth, M., De Martin, R. (2003): Functional screening for transcription factors (US20030059858A1). United States Patent Office.
Wiesner, C., Hoeth, M., Binder, B.R., de Martin, R. (2002): A functional screening assay for the isolation of transcription factors. Nucleic Acids Research, 30(16): e80.
Doi: https://doi.org/10.1093/nar/gnf079
Rohde, D., Wiesner, C., Graf, D. et al. (2000): Interstitial fluid pressure is increased in renal cell carcinoma xenografts. Urological Research, 28: 1-5.
Doi: https://doi.org/10.1007/s002400050001
Prof.(FH) Mag. Dr. Christoph Wiesner
Professor Department of Life Sciences
Dr.rer.nat.techn. Georg Sixta
Professor Department of Life Sciences
Institut Biotechnologie
+43 2732 802 351
[email protected]
IMC Campus KremsIMC Campus Trakt G
Applied Chemistry
Bachelor of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Master of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Dr.rer.nat.techn. Georg Sixta
Professor Department of Life Sciences
Prof.(FH) DI Dominik Schild
Professor Department of Life Sciences
Institut Biotechnologie
+43 2732 802 501
[email protected]
IMC Campus KremsIMC Campus Trakt G
Fermentationsentwicklung
Biochemische Verfahrenstechnik
Prozessingenieur
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Applied Chemistry
Bachelor of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Master of Science in Engineering / Vollzeit
Nachhaltiges biologisches Recycling von umweltbedenklichen Stoffen (Rare Earth Elements) aus Elektronikabfall und Abwässern
Projektleitung, Department of Life Sciences
Synthese und industrielle Verwendung von Hydroxytyrosol
Projektleitung, Department of Life Sciences
Extremophiles
Department of Life Sciences
Co-Kultivierung von Mikroorganismen
Projektleitung, Department of Life Sciences
Zellbasierte Testsysteme für bioaktive Substanzen
Department of Life Sciences
Hundsberger, H., Stierschneider, A., Sarne, V., Ripper, D., Schimon, J., Weitzenböck, H. P., Schild, D., Jacobi, N., Eger, A., Atzler, J., Klein, C. T., & Wiesner, C. (2021): Concentration-Dependent Pro- and Antitumor Activities of Quercetin in Human Melanoma Spheroids: Comparative Analysis of 2D and 3D Cell Culture Models. Molecules (Basel, Switzerland), 26(3): 717.
Doi: https://doi.org/10.3390/molecules26030717
Amer, H., Mimini, V., Schild, D., Rinner, U., Bacher, H., Potthast, A., Rosenau, T. (2019): Gram-scale economical synthesis of trans-coniferyl alcohol and its corresponding thiol. Holzforschung, 74(2): 197-202.
Doi: https://doi.org/10.1515/hf-2018-0297
Prof.(FH) DI Dominik Schild
Professor Department of Life Sciences
Dipl.Biol. Maren Pflüger, PhD
Wissenschaftliche Mitarbeit / Department of Life Sciences
Institut Biotechnologie
+43 2732 802 529
[email protected]
IMC Campus KremsIMC Campus Trakt D
Entzündung
Zytotoxizität
Wundheilung
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Extremophiles
Department of Life Sciences
Etablierung innovativer humaner Tumor-Mimetika für das Screening von bioaktiven Wirkstoffen
Department of Life Sciences
Biopharm - Isolation bioaktiver Stoffe aus Cyanobakterien
Department of Life Sciences
Zellbasierte Testsysteme für bioaktive Substanzen
Department of Life Sciences
Hundsberger, H., Koppensteiner, A., Hofmann, E., Ripper, D., Pflüger, M., Stadlmann, V., Klein, C. T., Kreiseder, B., Katzlinger, M., Eger, A., Forster, F., Missbichler, A., & Wiesner, C. (2017): A Screening Approach for Identifying Gliadin Neutralizing Antibodies on Epithelial Intestinal Caco-2 Cells. SLAS discovery : advancing life sciences R & D, 22(8): 1035–1043.
Doi: https://doi.org/10.1177/2472555217697435
Al-Harthy, T., Zoghaib, W. M., Pflüger, M., Schöpel, M., Önder, K., Reitsammer, M., Hundsberger, H., Stoll, R., & Abdel-Jalil, R. (2016): Design, Synthesis, and Cytotoxicity of 5-Fluoro-2-methyl-6-(4-aryl-piperazin-1-yl) Benzoxazoles. Molecules, 21(10): 1290.
Doi: https://doi.org/10.3390/molecules21101290
Al-Harthy, T., Abdel-Jalil, R., Zoghaib, W., Pflüger, M., Hofmann, E., & Hundsberger, H. (2016): Design and synthesis of benzothiazole schiff bases of potential antitumor activity. Heterocycles, 92(7): 1282-1292.
Doi: https://doi.org/10.3987/COM-16-13471
Kapuścik, A., Hrouzek, P., Kuzma, M., Bártová, S., Novák, P., Jokela, J., Pflüger, M., Eger, A., Hundsberger, H., Kopecký, J. (2013): Novel Aeruginosin-865 from Nostoc sp. as a potent anti-inflammatory agent. Chembiochem : a European journal of chemical biology, 14(17): 2329-2337.
Doi: https://doi.org/10.1002/cbic.201300246
Kreiseder, B., Orel, L., Bujnow, C., Buschek, S., Pflueger, M., Schuett, W., Hundsberger, H., de Martin, R., Wiesner, C. (2013): α‐Catulin downregulates E‐cadherin and promotes melanoma progression and invasion. International journal of cancer, 132(3): 521-530.
Doi: https://doi.org/10.1002/ijc.27698
Pflüger, M., Kapuscik, A., Lucas, R., Koppensteiner, A., Katzlinger, M., Jokela, J., Eger, A., Jacobi, N., Wiesner, C., Hofmann, E., Onder, K., Kopecky, J., Schütt, W., Hundsberger, H. (2013): A combined impedance and AlphaLISA-based approach to identify anti-inflammatory and barrier-protective compounds in human endothelium. Journal of biomolecular screening, 18(1): 67-74.
Doi: https://doi.org/10.1177/1087057112458316
Khare, V., Lyakhovich, A., Dammann, K., Lang, M., Borgmann, M., Tichy, B., Pospisilova, S., Luciani, G., Campregher, C., Evstatiev, R., Pflueger, M., Hundsberger, H., & Gasche, C. (2013): Mesalamine modulates intercellular adhesion through inhibition of p-21 activated kinase-1. Biochemical Pharmacology, 85(2): 234-244.
Doi: https://doi.org/10.1016/j.bcp.2012.10.026
Amatschek, S., Lucas, R., Eger, A., Pflueger, M., Hundsberger, H., Knoll, C., Grosse-Kracht, S., Schuett, W., Koszik, F., Maurer, D., Wiesner, C. (2011): CXCL9 induces chemotaxis, chemorepulsion and endothelial barrier disruption through CXCR3-mediated activation of melanoma cells. British journal of cancer, 104(3): 469-479.
Doi: https://doi.org/10.1038/sj.bjc.6606056
Hundsberger, H., Verin, A., Wiesner, C., Pflüger, M., Dulebo, A., Schütt, W., Lasters, I., Männel, D., Wendel, A., Lucas, R. (2008): TNF: a moonlighting protein at the interface between cancer and infection. Frontiers in Bioscience, 13: 5374-86.
Doi: https://doi.org/10.2741/3087
Hundsberger, H., Verin, A., Wiesner, C., Pflüger, M., Dulebo, A., Schütt, W., Lasters, I., Männel, D. N., Wendel, A., & Lucas, R. (2008): TNF: a moonlighting protein at the interface between cancer and infection. Frontiers in bioscience : a journal and virtual library, 13: 5374–5386.
Doi: https://doi.org/10.2741/3087
Wiesner, C., Pflueger, M., Kopecky, J., Stys, D., Entler, B., Lucas, R., Hundsberger, H., Schuett, W. (2008): Implementation of ECIS technology for the characterization of potential therapeutic drugs that promote wound-healing. GMS Krankenhaushygiene interdisziplinar, 3(1).
Wiesner, C., Pflüger, M., Kopecky, J., Stys, D., Entler, B., Lucas, R., Hundsberger, H., Schütt, W. (2008): Implementation of ECIS technology for the characterization of potential therapeutic drugs that promote wound-healing. GMS Krankenhaushygiene Interdisziplinär, 3(1): Doc05.
Wiesner, C., Lucas, R., Pflueger, M., Kleber, C., Kopecky, J., Stys, D., Entler, B., Hundsberger, H., Atzler, J., Hrouzek, P., Lukesova, A., Schuett, W., (2007): Endothelial Cell-Based Methods for the Detection of Cyanobacterial Anti- Inflammatory and Wound-Healing Promoting Metabolites. Drug Metabolism Letters, 1(4): 254-260.
Doi: https://doi.org/10.2174/187231207783221385
Lucas, R., Hundsberger, H., Pflueger, M., Fischer, B., Morel, D., Braun, C., Wendel, A., Chakraborty, T., Schuett, W., Wiesner, C., Hamacher, J. (2007): The Tumor Necrosis Factor-Derived TIP Peptide: A Potential Anti-Edema Drug. Letters in Drug Design & Discovery, 4(5): 336-340.
Doi: https://doi.org/10.2174%2F157018007780867816
Dipl.Biol. Maren Pflüger, PhD
Wissenschaftliche Mitarbeit / Department of Life Sciences
Prof.(FH) Mag. Dana Mezricky
Professorin Department of Life Sciences
Institut Biotechnologie
+43 2732 802 322
[email protected]
IMC Campus KremsIMC Campus Trakt G
GMP/GLP
Molekulare Biologie
Proteinchemie / Immunologie / Biochemische Alalysemethoden
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Master of Science in Engineering / Vollzeit
Nachhaltiges biologisches Recycling von umweltbedenklichen Stoffen (Rare Earth Elements) aus Elektronikabfall und Abwässern
Department of Life Sciences
Extremophiles
Department of Life Sciences
Co-Kultivierung von Mikroorganismen
Department of Life Sciences
Čížková, M., Mezricky, P., Mezricky, D., Rucki, M., Zachleder, V., Vítová, M. (2020): Bioaccumulation of Rare Earth Elements from Waste Luminophores in the Red Algae, Galdieria phlegrea. Waste Biomass Valor.
Doi: https://doi.org/10.1007/s12649-020-01182-3
Rezanka, T., Rezanka, M., Mezricky, D., Vítova, M. (2020): Lipidomic analysis of diatoms cultivated with silica nanoparticles. Phytochemistry, 177: 112452.
Doi: https://doi.org/10.1016/j.phytochem.2020.112452
Čížková, M., Mezricky, D., Rucki, M., Tóth, T. M., Náhlík, V., Lanta, V., Bišová, K., Zachleder, V., & Vítová, M. (2019): Bio-mining of Lanthanides from Red Mud by Green Microalgae. Molecules , 24(7): 1356.
Doi: https://doi.org/10.3390/molecules24071356
Řezanka, T., Kaineder, K., Mezricky, D., Řezanka, M., Bišová, K., Zachleder, V., & Vítová, M. (2016): The effect of lanthanides on photosynthesis, growth, and chlorophyll profile of the green alga Desmodesmus quadricauda. Photosynthesis Research, 130(1-3): 335-346.
Doi: https://doi.org/10.1007/s11120-016-0263-9
Prof.(FH) Mag. Dana Mezricky
Professorin Department of Life Sciences
DI (FH) Anita Koppensteiner
Wissenschaftliche Mitarbeit / Department of Life Sciences
Institut Biotechnologie
+43 2732 802 527
[email protected]
IMC Campus KremsIMC Campus Trakt D
Protein Produktion, Aufreinigung und Analyse
Zellbasierte Testsysteme/Mikroskopie
Biochemische Testmethoden und Analysen
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Applied Chemistry
Bachelor of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Master of Science in Engineering / Vollzeit
Nachhaltiges biologisches Recycling von umweltbedenklichen Stoffen (Rare Earth Elements) aus Elektronikabfall und Abwässern
Department of Life Sciences
Die Rolle von NFR2 in der Melanomprogression - Einblicke in die Mechanismen von Metastasen
Department of Life Sciences
Extremophiles
Department of Life Sciences
MEMESA – Metastasierendes Melanom Spezifische Antikörper
Department of Life Sciences
AdsorbTech: Entwicklung einer neuen Technologieplattform für Peptid-basierte therapeutische Apheresesysteme
Department of Life Sciences
Etablierung innovativer, vaskulärer Äquivalente zur Entwicklung von Detektionsmodulen für Hochdurchsatz-Verfahren und zur Entwicklung von anti-entzündlichen Peptiden
Department of Life Sciences
Hundsberger, H., Koppensteiner, A., Hofmann, E., Ripper, D., Pflüger, M., Stadlmann, V., Klein, C. T., Kreiseder, B., Katzlinger, M., Eger, A., Forster, F., Missbichler, A., & Wiesner, C. (2017): A Screening Approach for Identifying Gliadin Neutralizing Antibodies on Epithelial Intestinal Caco-2 Cells. SLAS discovery : advancing life sciences R & D, 22(8): 1035–1043.
Doi: https://doi.org/10.1177/2472555217697435
Schütz, B., Koppensteiner, A., Schörghofer, D., Kinslechner, K., Timelthaler, G., Eferl, R., Hengstschläger, M., Missbichler, A., Hundsberger, H., & Mikula, M. (2016): Generation of metastatic melanoma specific antibodies by affinity purification. Scientific reports, 6: 37253.
Doi: https://doi.org/10.1038/srep37253
Pflüger, M., Kapuscik, A., Lucas, R., Koppensteiner, A., Katzlinger, M., Jokela, J., Eger, A., Jacobi, N., Wiesner, C., Hofmann, E., Onder, K., Kopecky, J., Schütt, W., Hundsberger, H. (2013): A combined impedance and AlphaLISA-based approach to identify anti-inflammatory and barrier-protective compounds in human endothelium. Journal of biomolecular screening, 18(1): 67-74.
Doi: https://doi.org/10.1177/1087057112458316
DI (FH) Anita Koppensteiner
Wissenschaftliche Mitarbeit / Department of Life Sciences
Prof.(FH) Priv.Doz. Dr. Reinhard Klein
Professor Department of Life Sciences
Institut Biotechnologie
+43 2732 802 883
[email protected]
IMC Campus KremsIMC Campus Trakt G
Virologie
Molekjularbiologie
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Master of Science in Engineering / Vollzeit
In-Vivo-RNA Interferenzstrategien gegen Adenoviren
Projektleitung, Department of Life Sciences
Virale und fungale Infektionen
Projektleitung, Department of Life Sciences
RNA Interferenz als Methode zur Inhibierung von Virusinfektionen
Projektleitung, Department of Life Sciences
Selb, R., Derntl, C., Klein, R., Alte, B., Hofbauer, C., Kaufmann, M., Beraha, J., Schöner, L., & Witte, A. (2017): The Viral Gene ORF79 Encodes a Repressor Regulating Induction of the Lytic Life Cycle in the Haloalkaliphilic Virus ϕCh1. Journal of virology, 91(9): e00206-17.
Doi: https://doi.org/10.1128/JVI.00206-17
Derntl, C., Selb, R., Klein, R., Alte, B., & Witte, A. (2015): Genomic manipulations in alkaliphilic haloarchaea demonstrated by a gene disruption in Natrialba magadii. FEMS microbiology letters, 362(21): fnv179.
Doi: https://doi.org/10.1093/femsle/fnv179
Derntl, C., Selb, R., Klein, R., Alte, B., & Witte, A. (2015): Genomic manipulations in alkaliphilic haloarchaea demonstrated by a gene disruption in Natrialba magadii. FEMS microbiology letters, 362(21): fnv179.
Doi: https://doi.org/10.1093/femsle/fnv179
Bellutti, F., Kauer, M., Kneidinger, D., Lion, T., & Klein, R. (2015): Identification of RISC-associated adenoviral microRNAs, a subset of their direct targets, and global changes in the targetome upon lytic adenovirus 5 infection. Journal of virology, 89(3): 1608–1627.
Doi: https://doi.org/10.1128/JVI.02336-14
Bellutti, F., Kauer, M., Kneidinger, D., Lion, T., & Klein, R. (2015): Identification of RISC-associated adenoviral microRNAs, a subset of their direct targets, and global changes in the targetome upon lytic adenovirus 5 infection. Journal of virology, 89(3): 1608–1627.
Doi: https://doi.org/10.1128/JVI.02336-14
Ibrišimović, M., Lion, T., & Klein, R. (2013): Combinatorial targeting of 2 different steps in adenoviral DNA replication by herpes simplex virus thymidine kinase and artificial microRNA expression for the inhibition of virus multiplication in the presence of ganciclovir. BMC biotechnology, 13(1): 54.
Doi: https://doi.org/10.1186/1472-6750-13-54
Mayrhofer-Iro, M., Ladurner, A., Meissner, C., Derntl, C., Reiter, M., Haider, F., Dimmel, K., Rössler, N., Klein, R., Baranyi, U., Scholz, H., & Witte, A. (2013): Utilization of virus φCh1 elements to establish a shuttle vector system for Halo(alkali)philic Archaea via transformation of Natrialba magadii. Applied and environmental microbiology, 79(8): 2741–2748.
Doi: https://doi.org/10.1128/AEM.03287-12
Ibrišimović, M., Kneidinger, D., Lion, T., & Klein, R. (2013): An adenoviral vector-based expression and delivery system for the inhibition of wild-type adenovirus replication by artificial microRNAs. Antiviral research, 97(1): 10–23.
Doi: https://doi.org/10.1016/j.antiviral.2012.10.008
Kneidinger, D., Ibrišimović, M., Lion, T., & Klein, R. (2012): Inhibition of adenovirus multiplication by short interfering RNAs directly or indirectly targeting the viral DNA replication machinery. Antiviral research, 94(3): 195–207.
Doi: https://doi.org/10.1016/j.antiviral.2012.03.011
Ibrišimović, M., Nagl, U., Kneidinger, D., Rauch, M., Lion, T., & Klein, R. (2012): Targeted expression of herpes simplex virus thymidine kinase in adenovirus-infected cells reduces virus titers upon treatment with ganciclovir in vitro. The journal of gene medicine, 114(1): 3–19.
Doi: https://doi.org/10.1002/jgm.1638
Klein, R., Rössler, N., Iro, M., Scholz, H., & Witte, A. (2012): Haloarchaeal myovirus φCh1 harbours a phase variation system for the production of protein variants with distinct cell surface adhesion specificities. Molecular microbiology, 83(1): 137–150.
Doi: https://doi.org/10.1111/j.1365-2958.2011.07921.x
Klein, R., Ruttkowski, B., Schwab, S., Peterbauer, T., Salmons, B., Günzburg, W. H., & Hohenadl, C. (2008): Mouse mammary tumor virus promoter-containing retroviral promoter conversion vectors for gene-directed enzyme prodrug therapy are functional in vitro and in vivo. Journal of biomedicine & biotechnology, 2008(683505 ): 10.
Doi: https://doi.org/10.1155/2008/683505
Agu, C. A., Klein, R., Lengler, J., Schilcher, F., Gregor, W., Peterbauer, T., Bläsi, U., Salmons, B., Günzburg, W. H., & Hohenadl, C. (2007): Bacteriophage-encoded toxins: the lambda-holin protein causes caspase-independent non-apoptotic cell death of eukaryotic cells. Cellular microbiology, 9(7): 1753–1765.
Doi: https://doi.org/10.1111/j.1462-5822.2007.00911.x
Iro, M., Klein, R., Gálos, B., Baranyi, U., Rössler, N., & Witte, A. (2007): The lysogenic region of virus phiCh1: identification of a repressor-operator system and determination of its activity in halophilic Archaea. xtremophiles : life under extreme conditions, 11(2): 383–396.
Doi: https://doi.org/10.1007/s00792-006-0040-3
Klein, R., Ruttkowski, B., Knapp, E., Salmons, B., Günzburg, W. H., & Hohenadl, C. (2006): WPRE-mediated enhancement of gene expression is promoter and cell line specific. Gene, 372: 153–161.
Doi: https://doi.org/10.1016/j.gene.2005.12.018
Hand, N. J., Klein, R., Laskewitz, A., & Pohlschröder, M. (2006): Archaeal and bacterial SecD and SecF homologs exhibit striking structural and functional conservation. Journal of bacteriology,, 188(4): 1251–1259.
Doi: https://doi.org/10.1128/JB.188.4.1251-1259.2006
Agu, C. A., Klein, R., Schwab, S., König-Schuster, M., Kodajova, P., Ausserlechner, M., Binishofer, B., Bläsi, U., Salmons, B., Günzburg, W. H., & Hohenadl, C. (2006): The cytotoxic activity of the bacteriophage lambda-holin protein reduces tumour growth rates in mammary cancer cell xenograft models. The journal of gene medicine, 8(2): 229–241.
Doi: https://doi.org/10.1002/jgm.833
Mangold, M., Siller, M., Roppenser, B., Vlaminckx, B. J., Penfound, T. A., Klein, R., Novak, R., Novick, R. P., & Charpentier, E. (2004): Synthesis of group A streptococcal virulence factors is controlled by a regulatory RNA molecule. Molecular microbiology, 53(5): 1515–1527.
Doi: https://doi.org/10.1111/j.1365-2958.2004.04222.x
Rössler, N., Klein, R., Scholz, H., & Witte, A. (2004): Inversion within the genome of the haloalkaliphilic virus phiCh1 results in differential expression of structural proteins. Molecular microbiology, 52(2): 413–426.
Doi: https://doi.org/10.1111/j.1365-2958.2003.03983.x
Klein, R., Baranyi, U., Rössler, N., Greineder, B., Scholz, H., & Witte, A. (2002): Natrialba magadii virus fCh: First complete nucleotide sequence and functional organization of a virus infecting an extreme haloalkaliphilic archaeon. Molecular microbiology, 45(3): 851–863.
Doi: https://doi.org/10.1046/j.1365-2958.2002.03064.x
Klein, R., Greineder, B., Baranyi, U., & Witte, A. (2000): The structural protein E of the archaeal virus phiCh1: evidence for processing in Natrialba magadii during virus maturation. Virology, 276(2): 376–387.
Doi: https://doi.org/10.1006/viro.2000.0565
Baranyi, U., Klein, R., Lubitz, W., Krüger, D. H., & Witte, A. (2000): The archaeal halophilic virus-encoded Dam-like methyltransferase M. phiCh1-I methylates adenine residues and complements dam mutants in the low salt environment of Escherichia coli. Molecular microbiology, 35(5): 1168–1179.
Doi: https://doi.org/10.1046/j.1365-2958.2000.01786.x
Katinger, A., Lubitz, W., Szostak, M. P., Stadler, M., Klein, R., Indra, A., Huter, V., & Hensel, A. (1999): Pigs aerogenously immunized with genetically inactivated (ghosts) or irradiated Actinobacillus pleuropneumoniae are protected against a homologous aerosol challenge despite differing in pulmonary cellular and antibody responses. Journal of biotechnology, 73(2-3): 251–260.
Doi: https://doi.org/10.1016/s0168-1656(99)00143-1
Witte, A., Baranyi, U., Klein, R., Sulzner, M., Luo, C., Wanner, G., Krüger, D. H., & Lubitz, W. (1997): Characterization of Natronobacterium magadii phage phi Ch1, a unique archaeal phage containing DNA and RNA. Molecular microbiology, 23(3): 603–616.
Doi: https://doi.org/10.1046/j.1365-2958.1997.d01-1879.x
Szostak, M. P., Hensel, A., Eko, F. O., Klein, R., Auer, T., Mader, H., Haslberger, A., Bunka, S., Wanner, G., & Lubitz, W. (1996): Bacterial ghosts: non-living candidate vaccines. Journal of biotechnology, 44(1-3): 161–170.
Doi: https://doi.org/10.1016/0168-1656(95)00123-9
Prof.(FH) Priv.Doz. Dr. Reinhard Klein
Professor Department of Life Sciences
Prof.(FH) Dr. Christian Klein
Professor Department of Life Sciences
Institut Biotechnologie
+43 2732 802 522
[email protected]
IMC Campus KremsIMC Campus Trakt G
Wirkstoffdesign
Biochemische Systemtheorie
Molecular Modelling und Chemoinformatik
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Applied Chemistry
Bachelor of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Master of Science in Engineering / Vollzeit
Entwicklung von therapeutischen Peptiden für Krebs- und regenerative Medizin
Department of Life Sciences
Entwicklung einer Design-Pipeline für innovative Protein-Protein-Interaktionshemmer
Projektleitung, Department of Life Sciences
Entwicklung neuer immunregulierender Peptide und geschlechtsspezifischer organotypischer Zellmodelle für humane Sepsis
Department of Life Sciences
Funktionale Validierung prädiktiver Biomarker für zielgerichtete Krebstherapien
Department of Life Sciences
Hundsberger, H., Stierschneider, A., Sarne, V., Ripper, D., Schimon, J., Weitzenböck, H. P., Schild, D., Jacobi, N., Eger, A., Atzler, J., Klein, C. T., & Wiesner, C. (2021): Concentration-Dependent Pro- and Antitumor Activities of Quercetin in Human Melanoma Spheroids: Comparative Analysis of 2D and 3D Cell Culture Models. Molecules (Basel, Switzerland), 26(3): 717.
Doi: https://doi.org/10.3390/molecules26030717
Ablinger, C., Geisler, S. M., Stanika, R. I., Klein, C. T., & Obermair, G. J. (2020): Neuronal α2δ proteins and brain disorders. Pflugers Archiv : European journal of physiology, 472(7): 845-863.
Doi: https://doi.org/10.1007/s00424-020-02420-2
Jacobi, N., Smolinska, V., Seeboeck, R., Stierschneider, A., Klein, C., Hofmann, E., Wiesner, C., Mohr, T., Oender, K., Lechner, P., Kaiser, H., Hundsberger, H., Eger, A. (2017): 3D Anti-Cancer drug discovery models: A promising approach for precision medicine. In IMC Fachhochschule Krems GmbH (Hrsg.), Online-Tagungsband FHK Forschungsforum 2017. Krems: FFH.
Hundsberger, H., Koppensteiner, A., Hofmann, E., Ripper, D., Pflüger, M., Stadlmann, V., Klein, C. T., Kreiseder, B., Katzlinger, M., Eger, A., Forster, F., Missbichler, A., & Wiesner, C. (2017): A Screening Approach for Identifying Gliadin Neutralizing Antibodies on Epithelial Intestinal Caco-2 Cells. SLAS discovery : advancing life sciences R & D, 22(8): 1035–1043.
Doi: https://doi.org/10.1177/2472555217697435
Volk, K., Breunig, S. D., Rid, R., Herzog, J., Bräuer, M., Hundsberger, H., Klein, C., Müller, N., & Önder, K. (2017): Structural analysis and interaction studies of acyl-carrier protein (acpP) of Staphylococcus aureus, an extraordinarily thermally stable protein. Biological chemistry, 398(1): 125-133.
Doi: https://doi.org/10.1515/hsz-2016-0185
Hofmann, E., Seeboeck, R., Jacobi, N., Obrist, P., Huter, S., Klein, C., Oender, K., Wiesner, C., Hundsberger, H., & Eger, A. (2016): The combinatorial approach of laser-captured microdissection and reverse transcription quantitative polymerase chain reaction accurately determines HER2 status in breast cancer. Biomarker research, 7(4): 8.
Doi: https://doi.org/10.1186/s40364-016-0062-7
Jacobi, N., Smolinska, V., Stierschneider, A., Klein, C., Oender, K., Lechner, P., Kaiser, H., Hundsberger, H., Eger, A. (2016): Development of organotypic cancer models for the identification of individualized cancer therapies. In FH des BFI Wien (Hrsg.), Online-Tagungsband FHK Forschungsforum 2016. Wien: FFH.
Solca, F., Dahl, G., Zoephel, A., Bader, G., Sanderson, M., Klein, C.T., Kraemer, O., Himmelsbach, F., Haaksma, E., Adolf, G. R. (2012): Target Binding Properties and Cellular Activity of Afatinib (BIBW 2992), an Irreversible ErbB Family Blocker. Journal of Pharmacology and Experimental Therapeutics, 343(2): 342-350.
Doi: https://doi.org/10.1124/jpet.112.197756
Klein, C.T., Kaiser, D., Ecker, G. (2004): 3D Topolgical Distance-Based Descriptors for Use in QSAR and Diversity Analysis. Journal of Chemical Information and Computer Sciences, 44(1): 200-209.
Doi: https://doi.org/10.1021/ci0256236
Klein, C.T., Kaiser, D., Kopp, S., Chiba, P., Ecker, G. (2002): Similarity-Based SAR as Tool for Early ADME Profiling. Journal of Computer-Aided Molecular Design, 16: 785-793.
Doi: https://doi.org/10.1023/A:1023828527638
Klein, C.T., Kaiblinger, N., Wolschann, P. (2002): Internally Defined Distances in 3D-Quantitative Structure-Activity Relationships. Journal of Computer-Aided Molecular Design, 16: 79-93.
Doi: https://doi.org/10.1023/A:1016308417830
Mayer, B., Klein, C.T. (2000): Influence of Solvation on the Helix Forming Tendency of Nonpolar Amino Acids. Journal of Molecular Structure: THEOCHEM, 532(1-3): 213-226.
Doi: https://doi.org/10.1016/S0166-1280(00)00559-5
Buchbauer, G., Klein, C.T., Wailzer, B., Wolschann, P. (2000): Threshold-Based Structure-Activity Relationships of Pyrazines with Bell Pepper Flavor. Journal of Agricultural and Food Chemistry, 48(9): 4273-4278.
Doi: https://doi.org/10.1021/jf000192h
Klein, C.T., Polheim, D., Viernstein, H., Wolschann, P. (2000): A Method for Estimation of the Free Energies of Complexation between ß-Cyclodextrin and Guest Molecules. Journal of Inclusion Phenomena, 36(4): 409-423.
Doi: https://doi.org/10.1023/A:1008063412529
Klein, C.T., Pircher, H., Wailzer, B., Buchbauer, G., Wolschann, P. (2000): Quantitative Structure-Property Study on Pyrazines with Bell Peper Flavor. Scientific Pharmaceutica, 68(1): 41-56.
Doi: https://doi.org/10.3797/scipharm.aut-00-04
Klein, C.T., Lawtrakul, L., Hannongbua, S., Wolschann, P. (2000): Accessible Charges as Sensitive Descriptors in Structure-Activity Relationships. A Study on HEPT-based HIV-1 RT Inhibitors. Scientific Pharmaceutica, 68(1): 25-40.
Doi: https://doi.org/10.3797/scipharm.aut-00-03
Klein, C.T., Viernstein, H., Wolschann, P. (2000): Free Energy Prediction of Complexation between ß-Cyclodextrin and Guest Molecules: External Predictivity of MR and PLS Models. Scientific Pharamaceutica, 68(1): 15-24.
Doi: https://doi.org/10.3797/scipharm.aut-00-02
Klein, C.T., Polheim, D., Viernstein, H., Wolschann, P. (2000): Predicting the Free Energies of Complexation between Cyclodextrins and Guest Molecules: Linear versus Nonlinear Models. Pharamaceutical Research, 17: 358-365.
Doi: https://doi.org/10.1023/A:1007565409407
Mayer, B., Klein, C.T., Köhler, G. (1999): Selective Assembly of Cyclodextrins on Poly(ethylene oxide) Poly(propylene oxide) Copolymers. Journal of Computer-Aided Molecular Design, 13: 373-383.
Doi: https://doi.org/10.1023/A:1008095501870
Klein, C.T., Mayer, B. (1999): Sources for Switches and Structure Formation in Metabolic Pathways. Biosystems, 51(1): 41-52.
Doi: https://doi.org/10.1016/S0303-2647(99)00012-X
Klein, C.T., Mayer, B., Köhler, G., Wolschann, P. (1998): Systematic Stepsize Variation: An Efficient Method for Searching the Conformational Space of Polypeptides. Journal of Computational Chemistry, 19(13): 1470-1481.
Doi: https://doi.org/10.1002/(SICI)1096-987X(199810)19:13<1470::AID-JCC4>3.0.CO;2-N
Klein, C.T. (1998): Hysteresis-Driven Pattern Formation in Biochemical Networks. Journal of Theoretical Biology, 194(2): 263-274.
Doi: https://doi.org/10.1006/jtbi.1998.0757
Mayer, B., Marconi, G., Klein, C.T., Köhler, G., Wolschann, P. (1997): Structural Analysis of Host–Guest Systems. Methyl-substituted Phenols in beta;-Cyclodextrin. Journal of inclusion phenomena and molecular recognition in chemistry, 29: 79-93.
Doi: https://doi.org/10.1023/A:1007920606983
Klein, C.T., Mayer, B. (1997): A Model for Pattern Formation in Gap-Junction Coupled Cells. Journal of Theoretical Biology, 186(1): 107-115.
Doi: https://doi.org/10.1006/jtbi.1996.0337
Grabner, G., Monti, S., Marconi, G., Mayer, B., Klein, C.T., Köhler, G. (1997): Spectroscopic and Photochemical Study of Inclusion Complexes of Dimethoxybenzenes with Cyclodextrins. The Journal of Physical Chemistry , 100(51): 20068-20075.
Doi: https://doi.org/10.1021/jp962231r
Marconi, G., Mayer, B., Klein, C.T., Köhler, G. (1996): The structure of higher order C60-fullerene-γ-cyclodextrin complexes. Chemical Physics Letters, 260(5-6): 589-594.
Doi: https://doi.org/10.1016/0009-2614(96)00915-3
Köhler, G., Grabner, G., Klein, C.T., Marconi, G., Mayer, B., Monti, S., Rechthaler, K., Rotkiewicz, K., Viernstein, H., Wolschann, P. (1996): Structure and spectroscopic Properties in Cyclodextrin Inclusion Complexes. In Szejtli, J., Szente, L. (Hrsg.), Proceedings of the Eighth International Symposium on Cyclodextrins (215-220). Budapest, Hungary: Springer, Dordrecht.
Doi: https://doi.org/10.1007/978-94-011-5448-2_46
Klein, C.T., Mayer, B., Köhler, G., Wolschann, P. (1996): Influence of solvation on helix formation of poly-alanine studied by multiple annealing simulations. Journal of Molecular Structure: THEOCHEM, 372(1): 33-43.
Doi: https://doi.org/10.1016/S0166-1280(96)04745-8
Klein, C. T., & Seelig, F. F. (1995): Turing structures in a system with regulated gap-junctions. Bio Systems, 35(1): 15–23.
Doi: https://doi.org/10.1016/0303-2647(94)01478-p
Klein, C.T., Mayer, B., Köhler, G., Mraz, K., Reiter, S., Viernstein, H., Wolschann, P. (1995): Solubility and Molecular Modeling of Triflumizole-ß-cyclodextrin Inclusion Complexes. Journal of inclusion phenomena and molecular recognition in chemistry, 22: 15–32.
Doi: https://doi.org/10.1007/BF00706495
Prof.(FH) Dr. Christian Klein
Professor Department of Life Sciences
Prof.(FH) DI Bernhard Klausgraber
Professor Department of Life Sciences
Institut Biotechnologie
+43 2732 802 348
[email protected]
IMC Campus KremsIMC Campus Trakt G
Anorganische und Organische Chemie
Mikrobiologie
Fermentationsentwicklung und Optimierung
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Master of Science in Engineering / Vollzeit
Nachhaltiges biologisches Recycling von umweltbedenklichen Stoffen (Rare Earth Elements) aus Elektronikabfall und Abwässern
Department of Life Sciences
Synthese und industrielle Verwendung von Hydroxytyrosol
Department of Life Sciences
Extremophiles
Projektleitung, Department of Life Sciences
Co-Kultivierung von Mikroorganismen
Department of Life Sciences
Etablierung innovativer humaner Tumor-Mimetika für das Screening von bioaktiven Wirkstoffen
Department of Life Sciences
Prof.(FH) DI Bernhard Klausgraber
Professor Department of Life Sciences
Prof.(FH) Dr. Barbara Entler
Professorin Department of Life Sciences
Institut Biotechnologie
+43 2732 802 361
[email protected]
IMC Campus KremsIMC Campus Trakt G
Mikrobiologie
Mikrobielles Monitoring
Gentechnik
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Medical and Pharmaceutical Biotechnology
Master of Science in Engineering / Vollzeit
Nachhaltiges biologisches Recycling von umweltbedenklichen Stoffen (Rare Earth Elements) aus Elektronikabfall und Abwässern
Department of Life Sciences
Moritz, B., Locatelli, V., Niess, M., Bathke, A., Kiessig, S., Entler, B., Finkler, C., Wegele, H., & Stracke, J. (2017): Optimization of capillary zone electrophoresis for charge heterogeneity testing of biopharmaceuticals using enhanced method development principles. Electrophoresis, 38(24): 3136–3146.
Doi: https://doi.org/10.1002/elps.201700145
Wiesner, C., Pflueger, M., Kopecky, J., Stys, D., Entler, B., Lucas, R., Hundsberger, H., Schuett, W. (2008): Implementation of ECIS technology for the characterization of potential therapeutic drugs that promote wound-healing. GMS Krankenhaushygiene interdisziplinar, 3(1).
Wiesner, C., Pflüger, M., Kopecky, J., Stys, D., Entler, B., Lucas, R., Hundsberger, H., Schütt, W. (2008): Implementation of ECIS technology for the characterization of potential therapeutic drugs that promote wound-healing. GMS Krankenhaushygiene Interdisziplinär, 3(1): Doc05.
Wiesner, C., Lucas, R., Pflueger, M., Kleber, C., Kopecky, J., Stys, D., Entler, B., Hundsberger, H., Atzler, J., Hrouzek, P., Lukesova, A., Schuett, W., (2007): Endothelial Cell-Based Methods for the Detection of Cyanobacterial Anti- Inflammatory and Wound-Healing Promoting Metabolites. Drug Metabolism Letters, 1(4): 254-260.
Doi: https://doi.org/10.2174/187231207783221385
Prof.(FH) Dr. Barbara Entler
Professorin Department of Life Sciences
Prof. (FH) Dr. Maximilian Schachner
Stv. Leitung International Relations
International Relations
+43 2732 802 150
[email protected]
IMC Gozzoburg
Tourism and Leisure Management
Bachelor of Arts in Business / Vollzeit
Medical and Pharmaceutical Biotechnology
Bachelor of Science in Engineering / Vollzeit
Schwand, C., Berger, C., Hartbach, S., Kleiss, D., Kotek, K., Kormann, G., Schachner, M., & Neuherz, C. (2011): Grundelemente der Verkaufsraumgestaltung: Die Suche nach dem Stern. In FH Campus Wien (Hrsg.), Tagungsband 5. Forschungsforum der österreichischen Fachhochschulen, 27.-28. April 2011 (-). Wien: FFH.
Prof. (FH) Dr. Maximilian Schachner
Stv. Leitung International Relations

Zulassung & Aufnahme – die nächsten Schritte

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Ende der Bewerbungsfrist für EU StaatsbürgerInnen / Nachfrist	31.03.2021 / 10.05.2021
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Biotechnologie leicht erklärt

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Erfolgskonzept: Theorie + Praxis

1. Die Grundlagen

2. Das Praktikumssemester

3. Die Spezialisierung

Studienplan

Introduction to Laboratory Techniques

Applied Physics - Theory

Applied Physics - Laboratory

Analytical Chemistry Laboratory

Chemical Calculations

General and Inorganic Chemistry

Applied Mathematics - Theory

Applied Mathematics - Exercise

Introduction to Data Science I

Anatomy and Physiology

Human Genetics

Applied Microbiology

Microbiological Working Techniques Laboratory

Organic Chemistry - Theory

Organic Chemistry - Laboratory

Biostatistics

Introduction Data Science II

Applied Biophysics

Biophysics Laboratory

Human Diseases

Immunology and Medical Microbiology

Microbiological Monitoring Laboratory

Introduction to Contamination Control and Clean Room Training

Cell Biology

Molecular Biology and Genetic Engineering - Theory

Instrumental Analytics - Theory

Instrumental Analytics - Laboratory

Genetic Engineering Laboratory

Biochemistry - Theory

Biochemistry - Laboratory

Bioinformatics

Cell Physiology and Medical Molecular Biology

Cell Culture Techniques

Cell Culture Laboratory I

Bioprocess Technology Theory I

Measurement and Control Systems I

Introduction to Quality Management

GLP/GMP - Theory

Practical Training Application and Preparation

Cell Culture Laboratory II

Scientific Skills

Biochemical Analytics, Protein Purification

Equipment and Production Design

Bioprocess Technology Theory II

Fermentation and Bioseparation Laboratory, Data Analysis

GLP/GMP - Seminar

Genetic Engineering Laboratory under GLP

Practical Training Semester

Bachelor Seminar I

Pharmacology

Current Issues in Molecular Medicine

Project Management in Life Sciences

Journal Club for Current Issues

Introduction to Validation

Material Science and Biomaterials

Measurement and Control Systems II

Pharmaceutical Protein Production Systems

Journal Club for Current Issues

Principles of Management and Marketing

Clinical Studies and GCP

Drug Regulatory Affairs

Bachelor Seminar II and Bachelor Paper

Bachelor Exam

Besonderheiten

International studieren und arbeiten

Im Labor: Übung macht den Meister