320039 VO Separation and analysis methods for organic drug compounds (2013S)
Labels
Prüfungstermine:
28.06.2013 13.00 Uhr HS 7+8
30.09.2013 14.00 Uhr HS 7+8
31.10.2013 14.00 Uhr HS 7+8
09.01.2014 14.00 Uhr HS 8
28.06.2013 13.00 Uhr HS 7+8
30.09.2013 14.00 Uhr HS 7+8
31.10.2013 14.00 Uhr HS 7+8
09.01.2014 14.00 Uhr HS 8
Details
Language: German
Examination dates
-
Friday
24.05.2013
13:00 - 14:30
UZA2 Hörsaal 7 (Raum 2Z210) 2.OG
UZA2 Hörsaal 8 (Raum 2Z206) 2.OG - Friday 28.06.2013
-
Wednesday
02.10.2013
11:00 - 12:30
UZA2 Hörsaal 7 (Raum 2Z210) 2.OG
UZA2 Hörsaal 8 (Raum 2Z206) 2.OG -
Thursday
31.10.2013
14:00 - 15:30
UZA2 Hörsaal 7 (Raum 2Z210) 2.OG
UZA2 Hörsaal 8 (Raum 2Z206) 2.OG - Thursday 09.01.2014 14:00 - 15:30 UZA2 Hörsaal 8 (Raum 2Z206) 2.OG
- Friday 21.02.2014 14:00 - 15:30 UZA2 Hörsaal 8 (Raum 2Z206) 2.OG
Lecturers
Classes
Currently no class schedule is known.
Information
Aims, contents and method of the course
Assessment and permitted materials
Minimum requirements and assessment criteria
Examination topics
Reading list
Association in the course directory
A207
Last modified: Sa 02.04.2022 00:27
Aim: Acquisition of basic knowledge on the qualitative analysis of drug compounds with methods available in a pharmacy laboratory (proof of identity for drug compounds); knowledge about principles of function, applicability, and limitations of instrumental separation techniques (focus on chromatographic methods).
Contents: Determination of elemental composition, solubility, precipitation reactions, color reactions, identification of functional groups in drug compounds, physical properties, analysis of medicinal products (extraction of drug compounds, separation procedures); principles of chromatographic methods (separation mechanisms, classification of methods, theories of the chrom. process); individual chrom. methods: thin layer chromatography (TLC), column chrom. (CC), high performance liquid chrom. (HPLC), gas chrom. (GC); for each method: characteristic features, instrumentation, development techniques, detection methods, sample preparation, derivatisation; pharmaceutical applications; determination of separation performance, quantitative aspects (quantitation of elution curves and inner chromatograms, employment of internal and external standards); validation of chromatographic methods; reiated methods (SFC, CE, CEC).
Preconditions: successful completion of courses of the first study section; examinations on lectures from the second study section (3rd and 4th semester) can be done anyway (cf. Studienplan).
Mode of examination: written examination