3 ECTS credits
90 h study time

Offer 1 with catalog number 4013747ENR for all students in the 1st semester at a (E) Master - advanced level.

Semester
1st semester
Enrollment based on exam contract
Impossible
Grading method
Grading (scale from 0 to 20)
Can retake in second session
Yes
Taught in
Dutch
Faculty
Faculty of Sciences and Bioengineering Sciences
Department
Bio-Engineering Sciences
Educational team
Thierry Vandendriessche
Ken Broeckhoven (course titular)
Activities and contact hours
26 contact hours Lecture
Course Content

Part modeling of biomedical systems:

In this partim an answer to two important questions is given: What does the body do to a drug (pharmacokinetics) and what does a drug do to the body (pharmacodynamics). Using basic mathematical models, the time dependant absorption, distribution and elimination of drugs in the body and the quantitative physiological response of the body is modeled. The students also learn the importance of drug dose rate (including the effect of disease states) and administration method, with special attention to controlled drug release techniques.
 
 

Part Cellular engineering:

Basic aspects of Gene Therapy

1. Non-viral gene transfer methods:
- Stable vs. transient transfection (lipofection, calcium phosphate transfection, electroporation, …)
- Transposon-based technology (e.g. Sleeping beauty)

 

2. Viral gene transfer:
- Retroviral vectors
- Lentiviral vectors
- Adeno-associated viral vectors
- Cell-type specific targeting

- The production methods used to generate these different gene delivery vectors will be outlined in detail. This will also include a more practical approach to vector characterization.

- The properties of each of these gene delivery approaches in terms of efficacy and safety will be outlined in detail. Safety issues will focus on genotoxicity and immune consequences of gene transfer.

3. Concepts in gene transfer:
- ‘Gene editing’ with designer nucleases (ZFNs, CRISPR/Cas9, TALENs): targeted gene correction and integration in ‘safe harbour’ loci: ‘on-target’ & ‘off-target’ effects

- Genetic modification of somatic cells vs. germline cells

- Genetic modification of stem cells (iPS, ES, hematopoietic stem cells): pro’s and con’s for regenerative medicine applications


4. Gene therapy for monogenetic diseases (e.g. hemophilia, muscular dystrophy, Leber congenital amaurosis, hematopoietic disorders, …)

5. Gene therapy for neurodegenerative disorders

6. Gene therapy for cancer

Course material
Digital course material (Required) : Fysiologische engineering en cellulaire engineering, Notes
Digital course material (Required) : Handouts of powerpoint presentations, Canvas
Handbook (Recommended) : Pharmacokinetics made easy, Pocket Guide, D. J. Birkett, 2de, McGraw Hill Australia, 9780070285279, 2010
Additional info

Part Fysiological Engineering:

Handouts of powerpoint presentations and own notes (canvas)
 
Additional information (office Professor):
Pharmacokinetics made easy D. J. Birkett, McGraw Hill Australia, 2002, ISBN 0074710729
Basic Transport Phenomena in Biomedical Engineering, Chapter 7 (selected examples) Ronald L. Fournier
Handboek Of Pharmaceutical Controlled Release Technology, Chapters 10,11,22,23 (selected examples) 
Donald L. Wise
Pharmacokinetics: Processes, Mathematics, and Applications Peter G. Welling.
 
 
 
Part Cellular engineering:
 

Course material

  • Digital course material (Required): Powerpoint slides and articles are available on Canvas
  • Specific scientific articles

 

Additional info

Powerpoint slides are accessible through Canvas. The lectures will be conducted alternatingly on the Jette and Etterbeek campus with teleclassing, so that the students who are in Jette do not have to drive to Etterbeek and vice versa. The lectures that are taught in Jette will be transmitted ‘live’ to Etterbeek and vice versa. Discussions between the students and the lecturer and Q&A sessions can readily be implemented with this tele-classing modality.

 

Learning Outcomes

General competencies

Part modeling of biomedical systems:

 
The students learn the most important pharmacokinetic parameters.
 
The students understand the mechanism of drug transport in the human body.
 
The students are able to apply the pharmacokinetic parameters to predict the evolution of drug concentration in the human body.
 
The students can determine the required dose amount and speed of administration of a drug, taking disease states into account.
 
The students can predict the effect of non-linear pharmacokinetic behavior.
 
The students understand the relation between concentration and effect of a drug (pharmacodynamics).
 
The students understand the important of controlled-drug-release.
 
The students are able to explain the mechanisms that allow controlled-drug-release.
 

 

Part Cellular engineering:

- Having a fundamental knowledge of the descriptive and functional aspects of the molecular biological basis of gene therapy, gene transfer and gene editing in vitro and in vivo. This implies a level of knowledge and understanding that enables the student to design a biotechnological and biomedical research plan on gene therapy and gene editing.
 

- To achieve a critical attitude and attitude for scientific argumentation. To be able to practice the studied concepts independently and test these (for example through critical questions during lectures, through scientific papers that are available online and constitute the basis of the exam).

 

Grading

The final grade is composed based on the following categories:
Oral Exam determines 100% of the final mark.

Within the Oral Exam category, the following assignments need to be completed:

  • Oral. written prep. Fys. Eng. with a relative weight of 50 which comprises 50% of the final mark.

    Note: Part modeling of biomedical systems:
    oral exam with written preparation
  • Oral: Presentation Cell Eng. with a relative weight of 50 which comprises 50% of the final mark.

    Note: Part Gene Therapy & Gene Editing: presentation

Additional info regarding evaluation
Final results are the average of the grades obtained on the two parts
In order to pass the course, a miminum score of 10/20 has to be reached for each individual part.

 

Part modeling of biomedical systems:
Oral exam with written preparation

Part Cellular engineering:

Note: Knowledge and understanding are assessed by an oral exam based on a Powerpoint presentation of a scientific paper in the gene therapy field, published in one of the leading journals. The inter-relationship with and understanding of the course material is a key factor. Examinations are taken in Dutch or English, depending as to whether English-speaking students are attending the course.

 

Additional info regarding evaluation part Cellular engineering

 

The exam entails a 12 min presentation of an article of your choice based on the papers that are available on the Canvas platform in the Gene Therapy module. Typically, the talks should be based on maximum 15 slides. The talk is followed by an interactive session of  about 5 min, where you will be asked questions on (i) the content of the presentation and (ii) its relationship with the course (for example: if you choose a topic related to lentiviral vectors, you would need to know the properties of these vectors and how they are produced and justify why this particular vector was used in this study and not another one, like AAV). The Powerpoint slides of the Gene Therapy lectures are available on Canvas. 

 

The exam/presentation will take place outside the regular exam period.

 

The presentation has to be made using Powerpoint, keynote or a similar format and should encompass an introduction, objectives, results, conclusion. It should also include a critical assessment of the paper (i.e. what are the limitations of the study and how can we improve it?). 

 

The objective is really to assess whether you can apply the concepts that  you have learned in the lectures in a new context based on some of the top recent papers in the field in high impact factor journals (Nature journals, Science, New Engl J Med, etc. ...). All students from that group stay present during the entire session to ask questions in an interactive manner. The students have to provide a peer-assessment score for each presentation in their respective session. 

 

Your final mark will depend on:

 

1) Quality and structure of the slides

2) Clarity of the oral presentation

3) Answers to questions (Understanding of the course material)

4) Critical assessment of the paper's findings

+ Peer-assessment score
Allowed unsatisfactory mark
The supplementary Teaching and Examination Regulations of your faculty stipulate whether an allowed unsatisfactory mark for this programme unit is permitted.

Academic context

This offer is part of the following study plans:
Master of Bioengineering Sciences: Chemistry and Bioprocess Technology: Food Biotechnology (only offered in Dutch)
Master of Bioengineering Sciences: Chemistry and Bioprocess Technology: Chemical Biotechnology (only offered in Dutch)
Master of Bioengineering Sciences: Chemistry and Bioprocess Technology: Biochemical Biotechnology (only offered in Dutch)