KE517: Drug Formulation and Production A (10 ECTS)

STADS: 10009501

Level
Bachelor course

Teaching period
The course begins in the spring semester and continues in the autumn semester.

Teacher responsible
Email: kuntsche@sdu.dk

Additional teachers
mmb@sdu.dk
annette.bauer@sdu.dk

Timetable
Group Type Day Time Classroom Weeks Comment
H1 TL Monday 14-18 Lab 10 37-40
H1 TE Monday 14-16 U10 41
H1 TL Tuesday 14-18 Lab 10 37-41
H1 TE Thursday 10-12 U31 51 eksamensforberedelse
H1 TE Friday 10-11 U17 36
H1 TE Friday 10-11 U10 37
H1 TE Friday 10-11 U105 38
H1 TE Friday 10-11 U107 39
H1 TE Friday 10-11 U73 40
H2 TL Monday 08-12 Lab 10 37-40
H2 TE Monday 10-12 U10 41
H2 TE Tuesday 14-15 U103 37-40
H2 TL Tuesday 08-12 Lab 10 37-41
H2 TE Thursday 10-12 U31 51 eksamensforberedelse
H2 TE Friday 11-12 U17 36
H3 TE Monday 09-10 U10 41
H3 TE Tuesday 10-11 U57 38-40
H3 TL Thursday 12-16 Lab 10 37,39
H3 TL Thursday 14-18 Lab 10 38,40-41
H3 TE Thursday 14-16 U31 51 eksamensforberedelse
H3 TE Friday 15-16 U141 36
H3 TL Friday 14-18 Lab 10 37-40
H3 TE Friday 15-16 U49C 39 KE517 E-time H3
H3 TE Friday 10-12 U145 41
H4 TL Thursday 08-12 Lab 10 37-41
H4 TE Thursday 14-16 U31 51 eksamensforberedelse
H4 TE Friday 14-15 U69A 36-40
H4 TL Friday 08-12 Lab 10 37-40
H4 TE Friday 14-16 U10 41
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Prerequisites:
1st year test must be passed.

Academic preconditions:
BMB528 - Microbiology for Pharmaceutical Science is recommended known.

Course introduction
The aim of the course it to provide the participants with knowledge about the fundamental dosage forms with special focus on their formulation principles and production, about the requirements of the European Pharmacopoeia (Ph.Eur.) as well as the Danske Lægemiddelstandarder and about the impact of the physicochemical and chemical properties of active pharmaceutical ingredients and pharmaceutical excipients on the physical and biopharmaceutical characteristics of the dosage form and their stability.

Expected learning outcome
After the course, the student is expected to be able to:
  • demonstrate a broad overview over the requirements of the Ph.Eur. and properties of fundamental dosage forms together with their formulation principles and stability,
  • discuss the use of pharmaceutical excipients with regards to different dosage forms,
  • explain and discuss the function of pharmaceutical excipients in commercially available medicines,
  • apply and discuss fundamental biopharmaceutical principles and definitions, and
  • manufacture dosage forms in small scale together with documentation of the production.
Subject overview
  • General aspects on dosage forms (definitions, general functions of dosage forms, administration routes, general biopharmaceutical, physicochemical and therapeutic considerations)
  • Formulation and production of different dosage forms (liquid preparations for oral and cutaneous administration, powders, granules, tablets, capsules, parenteralia, eye preparations, semi-solid formulations for cutaneous application, herbal drugs, suppositories)
  • Physicochemical principles of the various dosage forms (solutions, suspensions, emulsions, solubility, solubilization, rheology, solid-state properties)
  • Microbiological quality of pharmaceutical preparations together with antimicrobial preservation and disinfection 
  • Relevant requirements and monographs of the European Pharmacopoeia (Ph.Eur.) and the Danske Lægemiddelstandarder (DLS) with regard to the different dosage forms mentioned above
  • Functions and structures of important pharmaceutical excipients and groups of excipients with regard to their function in the different dosage forms mentioned above
  • Extemporaneous preparations (DLS, documentation)
  • Biopharmaceutical aspects (bioavailability, LADME, plasma concentration curves together with relevant pharmacokinetic parameters, bioequivalence, dosage regimes)
  • Packing materials and stability
Literature
  • Churchill Livingstone Elsevier: Aulton’s Pharmaceutics
  • Europæiske Farmakopé (Ph.Eur.): Europæiske Farmakopé (Ph.Eur.), Danske Lægemiddelstandarder (DLS)., Kursusmaterialer (skal ligge på e-learn).


Website
This course uses e-learn (blackboard).

Prerequisites for participating in the exam
None

Assessment and marking:
Spring semester
  1. 4 mandatory theoretic seminars including homework with acceptable result for all homework and a written test at the end. Passed/fail, internal examination with teacher. In case of failure, a possibility of re-examination is provided in the same exam period or immediately thereafter (5 ECTS). (10009512)

Autumn semester

  1. 36 mandatory lab-exercises together with acceptance of 5 reports and a practical test at the end (preparation of a dosage form and documentation of preparation). Passed/failed, internal examination with teacher. In case of failure, a possibility of re-examination is provided in the same exam period or immediately thereafter (0 ECTS). (10009522)
  2. 2 hours written digital exam without aids (calculator is allowed). External examination. Marks according to the Danish 7-point marking scale. Re-examination in the same exam period or immediately thereafter (10 ECTS). (10009502)

The mode of exam at the re-examination may differ from the mode of exam at the ordinary exam.



Expected working hours
The teaching method is based on three phase model.
Intro phase: 46 hours
Skills training phase: 51 hours, hereof:
 - Tutorials: 14 hours
 - Laboratory exercises: 36 hours

Educational activities Study phase: 152 hours

Language
This course is taught in Danish or English, depending on the lecturer. However, if international students participate, the teaching language will always be English.

Course enrollment
See deadline of enrolment.

Tuition fees for single courses
See fees for single courses.