| Literature DB >> 27070830 |
Abstract
This review gives a brief introduction about the process- and product-related impurities and emphasizes on the development of novel analytical methods for their determination. It describes the application of modern analytical techniques, particularly the ultra-performance liquid chromatography (UPLC), liquid chromatography-mass spectrometry (LC-MS), high-resolution mass spectrometry (HRMS), gas chromatography-mass spectrometry (GC-MS) and high-performance thin layer chromatography (HPTLC). In addition to that, the application of nuclear magnetic resonance (NMR) spectroscopy was also discussed for the characterization of impurities and degradation products. The significance of the quality, efficacy and safety of drug substances/products, including the source of impurities, kinds of impurities, adverse effects by the presence of impurities, quality control of impurities, necessity for the development of impurity profiling methods, identification of impurities and regulatory aspects has been discussed. Other important aspects that have been discussed are forced degradation studies and the development of stability indicating assay methods.Keywords: Degradation studies; genotoxic impurities; impurity profiling; modern analytical techniques; stability indicating assay methods
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Year: 2016 PMID: 27070830 DOI: 10.1080/10408347.2016.1169913
Source DB: PubMed Journal: Crit Rev Anal Chem ISSN: 1040-8347 Impact factor: 6.535