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Abstract
This review highlights trends in the analysis of degradation and impurities in pharmaceuticals from 2008 to 2012.
- Analytical perspectives include forced degradation and impurity profiling of active pharmaceutical ingredients and drug products.
- Various analytical methods, including hyphenated techniques, are discussed for identifying and quantifying impurities.
- The review categorizes findings based on year of publication, type of chromatography, and therapeutic categories of drugs.
- Different pharmaceutical matrices, including APIs and dosage forms, are analyzed for their degradation profiles.
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