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About the Programme Academic Staff Program Qualifications Lessons Matrix of Course & Program Qualifications Turkish Qualifications Framework (TQF) TQF & Program Qualifications
  1. Graduate School
  2. Department of Pharmaceutical Technology
  3. Master of Science (MSc) in Biopharmaceutics and Pharmacokinetics
  4. Course Structure Diagram with Credits
  5. Pharmaceutical Dissolution Rate
  6. Description
  • Description
  • Learning Outcomes
  • ECTS Credit Load
  • Course's Contribution to Program
  • Learning Outcomes & Program Qualifications
Last Updated: 30/09/2026

Code - Course Title Course Type Laboratory + Practice ECTS
BFK503 - Pharmaceutical Dissolution Rate I. SEMESTER 3 +0 6.0
Language of Instruction Türkçe
Course Type Elective Courses
Course Instructor(s) PROF. DR. EBRU BAŞARAN
Mode of Delivery The mode of delivery of this course is face to face.
Place of Delivery
Used Educational Platforms
Prerequisites There is no prerequisite or co-requisite for this course.
Courses Recomended There is no recommended optional programme component for this course.
Recommended Resources
Work Placement Practical training is not required for this programme.
Aims of the Course

Weeks Learning Outcomes Topics Teaching Methods
Week - 1 In terms of dissolution test; gastrointestinal transit and drug absorption
Week - 2 Historical Development and Theory of Dissolution Testing - I
Week - 3 Historical Development and Theory of Dissolution Testing - II
Week - 4 Compendial requirements of dissolution testing
Week - 5 Compendial dissolution apparatuses - I
Week - 6 Compendial dissolution apparatuses - II
Week - 7 Calibration, qualification and sources of errors of compendia dissolution test apparatuses.
Week - 8 Fundamentals of dissolution test method development
Week - 9 Development of dissolution tests on the basis of gastrointestinal physiology
Week - 10 Development of a dissolution test method for quality control
Week - 11 Analysis of dissolution data for orally administered drug products
Week - 12 Dissolution test of heterogeneous dosage forms
Week - 13 Dissolution tests of aerosol type products
Week - 14 Dissolution testing to predict bioavailability and bioequivalence

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Assessment Method and Passing Requirements
Quamtity Percentage (%)
1.Midterm Exam 1 40
Final Exam 1 60
Toplam (%) 100

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