SLVKA0361U Pharmaceutical Analytical Chemistry
Volume 2013/2014
Education
MSc in Pharmaceutical
Sciences - compulsory, MSc in Medicinal Chemistry -
elective
Content
Study groups and
exercises constitute an integrated course package. The course
provides a background for selecting and developing analytical
methods and assessing the reliability of analytical data. A variety
of analytical techniques are described with regard to their use in
quantitative determination and identification. Teaching will focus
on the design and use of apparatus as well as potential sources of
error. There will also be focus on quality assurance and validation
of analytical methods, including the significance of linearity,
accuracy, precision, sensitivity, determination limits, blind
values, selectivity and interference. Study groups are used to
discuss theoretical background. The students take turns giving
30-minute presentations on theoretical subjects, which are
subsequently discussed and related to the practical experiments. In
the practical exercises, students work with fixed demonstrations of
separation and detection methods. They simultaneously work on a
project where they plan and try out a number of these techniques on
a given drug. The analytical techniques are liquid chromatography
(HPLC), gas chromatography (GC), capillary electrophoresis (CE),
UV-VIS spectrophotometry, fluorometry, mass spectrometry (MS),
atomic absorption spectrometry (AAS) and potentiometric methods.
The students carry out experiments in groups and submit a joint
report. Reports are assessed by the teacher and discussed on
return.
Learning Outcome
Formål / Objective
To enable students to develop and use analytical chemical methods in connection with development of drug substances, as well as identification and quality assessment of drugs and excipients.Målbeskrivelse / Course outcome
At the end of the course, students should:- Have adequate theoretical and practical knowledge of a wide variety of analytical chemical techniques to independently plan and perform quantitative determinations using relevant analytical methods
- Be able to explain the principle of the techniques, their areas of application and potential sources of error
- Master the methodological terminology required for reading literature and writing reports
- Master quantitative calculations based on various calibration methods in connection with the analytical chemical methods applied
- Be able to assess the reliability of analytical data
- Be able to report experiments briefly, clearly and unambiguously.
Literature
- D.C. Harris: Quantitative Chemical Analysis, latest edition, W.H. Freeman and Company, New York.
- Compendium in Pharmaceutical Analytical Chemistry, latest edition, Department of Pharmacy, University of Copenhagen. Is available on the course home page via Absalon.
Academic qualifications
Students must have
accumulated at least 15 ECTS credits in chemical subjects, of which
10 ETCS credits must be in the field of organic
chemistry.
Teaching and learning methods
•Exercises/project: 16
four-hour sessions plus report writing
•Study groups: 8 two-hour sessions
•Study groups: 8 two-hour sessions
Workload
- Category
- Hours
- Colloquia
- 6
- Practical exercises
- 55
- Preparation
- 39
- Project work
- 106
- Total
- 206
Sign up
Compulsory for line 2 of the MSc
programme in Pharmaceutical Sciences.
Exam (Pharmaceutical Analytical Chemistry)
The student demonstrates a high-level command of all aspects of the relevant material, with no or only a few minor weaknesses. 7 - Good performance
The student demonstrates a good command of the relevant but also some weaknesses. 2 - Acceptable performance
The student meets only the minimum requirements.
- Credit
- 7,5 ECTS
- Type of assessment
- Oral examination under invigilationPrøveform / Examination type:
Individual oral based on reports from the laboratory exercises.
Prøvedesign / Examination design
Individual oral exam with preparation time. The student is examined on the basis of two reports selected by lot. After the report selection, the student has 30 minutes’ preparation time with the help of all written materials.
Særlige forhold / Special conditions:
Registration for the exam is contingent on approval of all reports from the laboratory exercises. - Marking scale
- 7-point grading scale
- Censorship form
- External censorship
Criteria for exam assesment
Beskrivelse af prøven og bedømmelse / Description of examination and assessment criteria
Beståkrav / Pass criteria
To pass the exam, the student should be able to describe the analytical methods applied in the selected reports and demonstrate ability to perform quantitative determinations based on analytical data.Karakterbeskrivelse / Description of grades
12 - Excellent performanceThe student demonstrates a high-level command of all aspects of the relevant material, with no or only a few minor weaknesses. 7 - Good performance
The student demonstrates a good command of the relevant but also some weaknesses. 2 - Acceptable performance
The student meets only the minimum requirements.
Course information
- Language
- English
- Course code
- SLVKA0361U
- Credit
- 7,5 ECTS
- Level
- Full Degree Master
- Duration
- 1 block
- Placement
- Block 3
- Schedule
- A
- Course capacity
- 30 students
- Study board
- Study Board of Pharmaceutical Sciences
Contracting department
- Department of Pharmacy
Course responsibles
- Christian Janfelt (christian.janfelt@sund.ku.dk)
Saved on the
02-05-2013