Study Of Stress Induced Degradation In Anticancer Drugs Lcms MS Analysis And Stability Indicating HPLC Method Development

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dc.contributor.guidePraveen Kumar
dc.coverage.spatial
dc.creator.researcherSachin Chawla
dc.date.accessioned2024-06-27T04:51:44Z
dc.date.available2024-06-27T04:51:44Z
dc.date.awarded2024
dc.date.completed2024
dc.date.registered2020
dc.description.abstractDrug formulations contain active pharmaceutical ingredients (APIs) and excipients. APIs present in the formulations contain some undesired impurity, which affects purity of the APIs. Therefore, along with % purity, impurity profiling is also needed to be carried out of all the APIs. Impurity profiling describes the account or description of maximum possible types of identified or unidentified impurities present in any APIs. These impurities can be API related impurities, process related impurities or stability related impurities. API related impurities include stereochemistry, crystallization, and functional group of APIs. Process related impurities include chemicals, reagents, catalysts, residual solvents, synthetic intermediate products, by product, degradation products, method conditions related impurities, and formulation related impurities. newline
dc.description.noteAnticancer Drugs
dc.format.accompanyingmaterialDVD
dc.format.dimensions
dc.format.extent
dc.identifier.urihttp://hdl.handle.net/10603/573697
dc.languageEnglish
dc.publisher.institutionGlocal School of Science
dc.publisher.placeSaharanpur
dc.publisher.universityGlocal University
dc.relation
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordChemistry
dc.subject.keywordChemistry Applied
dc.subject.keywordPhysical Sciences
dc.titleStudy Of Stress Induced Degradation In Anticancer Drugs Lcms MS Analysis And Stability Indicating HPLC Method Development
dc.title.alternativeStudy Of Stress Induced Degradation In Anticancer Drugs Lcms MS Analysis And Stability Indicating HPLC Method Development
dc.type.degreePh.D.

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