Analytical Method Development for Related Substances in Pharmaceutically Important Bulk Drugs and Intermediates

dc.contributor.guide	Paradesi, D
dc.creator.researcher	Suresh Babu, K
dc.date.accessioned	2022-12-13T07:17:18Z
dc.date.available	2022-12-13T07:17:18Z
dc.date.awarded	2022
dc.date.completed	2022
dc.description.abstract	In pharmaceutical industry, impurity profile is mandatory requirement for drug products. Typically, impurity profile of drugs consisting of both identified and unidentified impurities. Appropriate high performance liquid chromatography (HPLC) and gas chromatography (GC) techniques support for generating an impurity profile and finalised conditions will be standardized to detect all the impurities present in the product. This procedure involves selecting a suitable column, optimizing the mobile phase pH, finalising the flow rate, selecting the type of detector and maintaining column temperature. Once the conditions are optimized for a particular product and its impurity profile will be standardized.
dc.format.accompanyingmaterial	DVD
dc.identifier.uri	http://hdl.handle.net/10603/425214
dc.language	English
dc.publisher.institution	Department of Chemistry
dc.publisher.place	Kattankulathur
dc.publisher.university	SRM Institute of Science and Technology
dc.rights	university
dc.source.university	University
dc.subject.keyword	Chemistry
dc.subject.keyword	Chemistry Analytical
dc.subject.keyword	Physical Sciences
dc.title	Analytical Method Development for Related Substances in Pharmaceutically Important Bulk Drugs and Intermediates
dc.type.degree	Ph.D.