Project Work In Pharmaceutics And Industrial Pharmacy Department
Pharmaceutics project work |
Pharmaceutics project is one of the broadest in terms of topics. In fact, hardly will a student be given a project work that has been work on before. However, the topics have little variations, as the process is always similar with previous works.
Get to know your project supervisor, your project topic, and an approved project proposal. Once this stage is accomplished, the next process is to determine which aspect of the project you are going to use. It ranges from the survey, research in trends and bench work.
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Survey In Project
The production of a suitable dosage form for individuals is the core function of this department. The suitability of these drugs can be analysed in the laboratory. However, users’ reactions are the best way to analyse this parameter. The survey method depends on the approved type for the topic by the supervisor. Some of the information needed include the time of action of the drug, reactions, side effects etc. on humans.Research In Trends
This is a way to investigate what other scientist has done on pharmaceutics work. It could mean comparing the different types of drug design and how effective they are, based on results from past project. Some others can involve examining new and old production process, methods of writing agreements in pharmaceutical industries.Bench Work
Bench work usually involves analyzing the effect of an excipient in a particular product. The project work will depend on the excipients under investigation. If it involves investigating the effect of a new sweetening agent, binder, gum etc., the process is similar. It starts with extracting the excipients. The extract of the excipient in the pharmacognosy laboratory is used for the project instead of a standard known excipient. For a project involving using chemical compounds as excipients, they can be isolated in a chemistry laboratory.The extract is processed maybe by drying. The medicinal drug is processed into a dosage form. It could be a liquid, solid or semi-solid. To understand the production process of these dosage forms, you can refer to any standard pharmaceutical codex.
After production, evaluate and characterize the new product using some equipment in the laboratory. This includes hardness test, solubility test etc. after which the result is compared with a standard and reported.
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However, there are sometimes, the project product may need to be studied for its effects on microorganisms or animals. The product in pharmaceutical microorganisms or pharmacology laboratory analyses for its effects on microorganism and animals respectively. The result is compared with a standard during project report.
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