SFAK20014U Cancelled Principles and Practice of Bioanalysis

Volume 2021/2022
Education

MSc Programme in Pharmacy (Danish programme cand.pharm) - elective

MSc Programme in Pharmaceutical Sciences (Danish programme cand.scient.pharm) - restricted elective

MSc Programme in Medicinal Chemistry - elective

MSc Programme in Pharmaceutical Sciences (English programme)- restricted elective 

MSc Programme in Environmental Science (SCIENCE) - restricted elective

Content

The course is intended for (a) students specializing in bioanalysis (determination of pharmaceuticals in biological fluids), for (b) students with need for improved general knowledge and skills in analytical chemistry / pharmaceutical chemical analysis, and for (c) students specializing in drug metabolism. Students according to (b) and (c)  are typically master students using analytical techniques during the experimental work for the master thesis. The course focuses both on theoretical and practical aspects of bioanalysis.

The first part of the course teaches the principles of major bioanalytical techniques at high level (lectures):

  • Sample preparation (protein precipitation, liquid extraction, solid-phase extraction)
  • Liquid chromatography
  • Liquid chromatography-mass spectrometry
  • Gas chromatography
  • Gas chromatography-mass spectrometry
  • Capillary electrophoresis

The second part of the course teaches the use of the above techniques at high level for the following purposes (lectures):

  • Determination of small molecule pharmaceuticals and their metabolites in biological fluids (blood, urine, saliva, dried blood spots)
  • Determination of biopharmaceuticals in biological fluids
  • In-vitro metabolism studies of small molecule pharmaceuticals

Application areas include therapeutic drug monitoring, in-vitro metabolism studies, forensic toxicology, and doping analysis.

The third part of the course focus on reading and understanding research articles in bioanalysis related to the techniques and applications outlined above, and include student presentation of selected articles.

The fourth part of the course comprises laboratory exercises related to the techniques and applications outlined above.

Learning Outcome

At the end of the course, students are expected to be able to:

Knowledge

  • Have an in-depth theoretical understanding of the major techniques used in bioanalysis of pharmaceuticals and their metabolites
  • Understand the individual steps in procedures for determination of small molecule pharmaceuticals and biopharmaceuticals in biological fluids
  • Understand the individual steps of in-vitro metabolism studies of small molecule pharmaceuticals

 

Skills

  • Be able to perform practical bioanalytical work according to published / existing procedures
  • Know and be able to use a broad number of separation and detection principles as well as sample preparation techniques used for bioanalysis.
  • Understand the principles behind and use the analytical chemical instrumentation needed for high sensitivity analysis of samples of biological origin.
  • Judge and use the relevant original analytical chemical literature, handbooks and databases.

 

Competences

  • Understand and perform bioanalytical chemical work.
  • Develop new analytical chemical methods for analysis of samples of biological origin (e.g. urine, plasma, serum, faeces, saliva, synovial liquid, plant materials etc.).
  • Design sampling and storage protocols for in vivo studies of drug metabolism.
  • Steen Honore Hansen, Stig Pedersen-Bjergaard: Bioanalysis of Pharmaceuticals: Sample Preparation, Chromatography and Mass Spectrometry, ISBN: 978-1-118-71682-3, Wiley (2015)
  • Additional course materials such as manuals and scientific papers are availabe from the course homepage
If you are applying for the course as a credit transfer student, you must have passed SFAB20035U Farmaceutisk analytisk kemi or have acquired similar competencies in another course. Documentation for corresponding competencies in the form of a course description and an exam result must be attached to your application.
Course teaching is based upon the assumption that the student has general knowledge within the areas of organic chemistry, inorganic chemistry, physical chemistry, analytical chemistry, biochemistry, pharmacology, toxicology, and drug development at bachelor level.
Lectures: 32 hours
Laboratory exercises: 24 hours
  • Category
  • Hours
  • Lectures
  • 36
  • Preparation
  • 146
  • Practical exercises
  • 24
  • Total
  • 206
Oral
Collective
Credit
2,5 ECTS
Type of assessment
Continuous assessment
In order to obtain the course certificate the student should participate actively during laboratory exercises, complete all the laboratory exercises and make an oral satisfying presentation of the "Independent Study Activity".
Marking scale
passed/not passed
Censorship form
No external censorship
Criteria for exam assesment

To achieve a course certificate the student must be able to:

Knowledge

  • Have an in-depth theoretical understanding of the major techniques used in bioanalysis of pharmaceuticals
  • Understand the individual steps in procedures for determination of small molecule pharmaceuticals and biopharmaceuticals in biological fluids
  • Understand the individual steps of in-vitro metabolism studies of small molecule pharmaceuticals

 

Skills

  • Be able to perform practical bioanalytical work according to published / existing procedures
  • Know and be able to use a broad number of separation and detection principles as well as sample preparation techniques used for bioanalysis.
  • Understand the principles behind and use the analytical chemical instrumentation needed for high sensitivity analysis of samples of biological origin.
  • Judge and use the relevant original analytical chemical literature, handbooks and databases.

 

Competences

  • Understand and perform bioanalytical chemical work.
  • Develop new analytical chemical methods for analysis of samples of biological origin (e.g. urine, plasma, serum, faeces, saliva, synovial liquid, plant materials etc.).
  • Design sampling and storage protocols for in vivo studies of drug substances.

 

In the "Exam 1" the students are evaluated from the participation in the laboratory exercises as well their "Independent Study Activity" where they critically present analytical chemical literature.

Credit
5 ECTS
Type of assessment
Written examination, 2 hours under invigilation
Examination type:
2 hour multiple-choice test. The students are evaluated in a multiple choice examination that covers questions related to the lab exercices, lectures and student presentations.
Aid
Written aids allowed

There is access to the following at the exam at KU's exam venue:

  • R – Statistical programme
  • ChemDraw
  • MathType formel programme
  • Maple
  • Digital Notes (It is allowed to upload notes for the ITX exam via digital exam. You will find a link to this feature from your exam in Digital Exam).

Marking scale
passed/not passed
Censorship form
No external censorship
Criteria for exam assesment

To pass the course the student must be able to:

Knowledge

  • Have an in-depth theoretical understanding of the major techniques used in bioanalysis of pharmaceuticals
  • Understand the individual steps in procedures for determination of small molecule pharmaceuticals and biopharmaceuticals in biological fluids
  • Understand the individual steps of in-vitro metabolism studies of small molecule pharmaceuticals

 

Skills

  • Be able to perform practical bioanalytical work according to published / existing procedures
  • Know and be able to use a broad number of separation and detection principles as well as sample preparation techniques used for bioanalysis.
  • Understand the principles behind and use the analytical chemical instrumentation needed for high sensitivity analysis of samples of biological origin.
  • Judge and use the relevant original analytical chemical literature, handbooks and databases.

 

Competences

  • Understand and perform bioanalytical chemical work.
  • Develop new analytical chemical methods for analysis of samples of biological origin (e.g. urine, plasma, serum, faeces, saliva, synovial liquid, plant materials etc.).
  • Design sampling and storage protocols for in vivo studies of drug substances.