Module Specifications.
Current Academic Year 2024 - 2025
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Date posted: September 2024
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Repeat the module |
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Description In this module students will be introduced to a regulated laboratory environment where they will carry out typical pharmaceutical laboratory experiments, and to the practice of auditing data according to SOP and compendia. Students will be introduced to the analytical techniques which are used on a daily basis within the pharmaceutical industry. Students will be also introduced to the topics of rearrangements and retrosynthesis which will be further explored in practical experiments. | |||||||||||||||||||||||||||||||||||||||||||||
Learning Outcomes 1. Execute the analysis of pharmaceutical raw materials at a Regulatory standard. 2. Undertake and properly interpret in vitro dissolution profiles of a final formulated drug product. 3. Show a high competency skill level in performing essential analytical methods that are used within the pharmaceutical industry 4. Design reasonable synthetic pathways through appropriate retrosyntheses and forward syntheses. 5. Set up reactions and monitor their progress, and work up and purify reaction products, using a combination of fundamental and advanced laboratory techniques. 6. Accurately record laboratory procedures and results and produce high quality reports detailing relevant information. 7. Appropriately interprete the collected data. | |||||||||||||||||||||||||||||||||||||||||||||
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
Experiments performed in the Analytical part:1. Spectroscopic Determination of Iron in Iron Tablets. 2. Esterification of Carboxylic Acids and Analysis by Capillary GC-FID. 3. Comparison studies of analytical methods: Magnesium in pharmaceutical preparations by Atomic Absorption and Titrimetry.Experiments performed in the Pharmaceutical part:1. Testing of raw materials used in the manufacture of the Panadol 500mg Tablets. 2. Dissolution testing and further method validation testing. 3. Assay of active ingredient in Panadol 500mg tablets using the Varian automated photo-diode array HPLC system.Experiments performed in the Organic part:1. Isoxazoline and Wittig reactions. 2. Regioselective hydroboration via Brown hydroboration. 3. Synthesis of alkenes using the Horner Wadsworth Emmons reaction. | |||||||||||||||||||||||||||||||||||||||||||||
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Indicative Reading List
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Other Resources 45281, Website, MIT, 2007, Digital Lab Techniques Manual, https://ocw.mit.edu/resources/res-5-0001-digital-lab-techniques-manual-spring-2007/videos/, | |||||||||||||||||||||||||||||||||||||||||||||