Module Specifications.
Current Academic Year 2024 - 2025
All Module information is indicative, and this portal is an interim interface pending the full upgrade of Coursebuilder and subsequent integration to the new DCU Student Information System (DCU Key).
As such, this is a point in time view of data which will be refreshed periodically. Some fields/data may not yet be available pending the completion of the full Coursebuilder upgrade and integration project. We will post status updates as they become available. Thank you for your patience and understanding.
Date posted: September 2024
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Repeat examination Array |
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Description To introduce students to drug action. To introduce students to the basic concepts of drug design and what physicochemical properties of a molecule are important in therapeutic action. To introduce students to empirical methods which are used in drug design and invention. To introduce students to the important principles of drug delivery and what biological factors affect these processes. To introduce students to elementary pharmacokinetics and drug metabolism | |||||||||||||||||||||||||||||||||||||||||||
Learning Outcomes 1. Recognise the importance of understanding the biological nature of a disease in order to develop effective drug treatments. 2. Use both structure activity relationships and quantitative structure activity relationships to develop new drug candidates. 3. Value the importance of bioavailability in the discovery of new drug candidates. 4. Use modern synthetic methods and strategies to create libraries of molecules for drug screening. | |||||||||||||||||||||||||||||||||||||||||||
All module information is indicative and subject to change. For further information,students are advised to refer to the University's Marks and Standards and Programme Specific Regulations at: http://www.dcu.ie/registry/examinations/index.shtml |
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Indicative Content and Learning Activities
IntroductionReview of Drug action, classification, sources and development and production.Drug Design: Conformation, stereochemistry, configuration.Structure-activity Relationships (SAR/QSAR) - Shape and size, substituents, partition coefficients, Hammett constants, Taft steric parameters, Methods based on Hansch and related approaches.Empirical Drug Design : Search for Lead Compounds; Natural Sources/Serendipity; Systematic Search; Combinatorial Libraries. Chemical Aspects of Drug Delivery: An integral part of drug action/design. Solubilities, pKa's and pH will be discussed and it's effect on drug design.Biological Membranes and Enzymes: Impact on drug design. Distribution, Elementary Pharmacokinetics and Drug Metabolism: Use in drug design. Specific examples of drugs will be used. | |||||||||||||||||||||||||||||||||||||||||||
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Other Resources None | |||||||||||||||||||||||||||||||||||||||||||