P224T : Pharmaceutics II

Department

faculty of Pharmacy

Academic Program

Bachelor in pharmaceutical sciences

Type

Compulsory

Credits

03

Prerequisite

P223PT

Overview

This course introduces the concepts of dosage forms design in laboratories or manufacturers. As it explains the basic principles of formulation and pre-formulation process for different dosage forms. It also includes the identification of physiochemical aspects of ingredients with their practical application. It will focus on some examples of excipients. The aims of this course are:

  • Understanding the reasons for the need to design dosage forms as well as the general points that must be considered when designing dosage forms
  • Knowing the concept of dosage forms, the rationale for the development of a particular dosage form, and the different types of dosage forms
  • Understanding the advantages and disadvantages of each route of administration
  • Knowing liquid dosage forms and their classifications: single-phase formulations, for example, solutions, and multi-phase formulations, such as suspensions
  • Knowing the forms of pharmaceutical solutions, their main components, methods of preparation, selection of appropriate packaging, and appropriate storage conditions
  • knowing the concept of dispersion such as rheology of suspensions, selection of thickening agents, learning the DLVO theory that explains the stability of dispersion systems and the types of interactions between molecules, and the different tests to evaluate the stability of suspensions.

Intended learning outcomes

Upon completion of the course, the student will be:

  • familiar with: the basic concepts related to the formulation and pre-formulation of pharmaceutical dosage forms and the difference between active pharmaceutical ingredients and various additive
  • familiar with: the different physical and chemical factors, the materials, and the different methods for designing and manufacturing these pharmaceutical products.
  • familiar with: the different types of pharmaceutical dosage forms, the various ways of administration, the most appropriate packaging, the appropriate storage condition, and the factors affecting the stability of the pharmaceutical products
  • familiar with: the liquid dosage forms, their classifications, their main components, and their methods of preparation.
  • familiar with various tests that are used to evaluate the stability of suspensions.

Teaching and learning methods

Lectures/ lab classes/ group discussions.

Methods of assessments

The students' knowledge and performance about the studied topics are assessed throughout the study period. These assessment methods include the following quizzes, oral exams, and written exams (grand total mark 100%)

  • Mid-term exam =20%
  • Practical and oral exams =20%
  • activities =20%
  • Final exam =40%

References:

Aulton, M. E., & Taylor, K. (2002). Pharmaceutics-The Science of Dosage Form Design. Churchill Livingstone. London, England.