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Volumn 36, Issue 1, 2012, Pages 61-79
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Identification of prasugrel (an antiplatelet drug) impurities by LC-MS/MS, rapid determination of prasugrel hydrochloride-related substances, and degradation products in active pharmaceutical ingredient and pharmaceutical dosage forms by stability indicating ultra-performance liquid chromatographic method
a,b
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Author keywords
forced degradation; identification by LC MS MS; Prasugrel hydrochloride; stability indicating; UPLC; validation
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Indexed keywords
BYPRODUCTS;
CHROMATOGRAPHIC ANALYSIS;
DEGRADATION;
DRUG DOSAGE;
DRUG PRODUCTS;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
IMPURITIES;
ISOMERS;
DEGRADATION PRODUCTS;
FORCED DEGRADATION;
IDENTIFICATION BY LC/MS/MS;
LC-MS-MS;
PERFORMANCE;
PRASUGREL;
PRASUGREL HYDROCHLORIDE;
STABILITY-INDICATING;
ULTRA-PERFORMANCE LIQUID CHROMATOGRAPHIC;
VALIDATION;
LIQUIDS;
PRASUGREL;
ACIDITY;
ANALYTIC METHOD;
ARTICLE;
CHEMICAL STRESS;
CHEMICAL STRUCTURE;
DRUG DEGRADATION;
DRUG DETERMINATION;
DRUG DOSAGE FORM;
DRUG IMPURITY;
DRUG STABILITY;
HYDROLYSIS;
OXIDATIVE STRESS;
PHOTOLYSIS;
PRACTICE GUIDELINE;
PROCESS DEVELOPMENT;
REPRODUCIBILITY;
REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
SEPARATION ANXIETY;
TANDEM MASS SPECTROMETRY;
TEMPERATURE STRESS;
ULTRA PERFORMANCE LIQUID CHROMATOGRAPHY;
VALIDITY;
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EID: 84872362722
PISSN: 10826076
EISSN: 1520572X
Source Type: Journal
DOI: 10.1080/10826076.2011.644052 Document Type: Article |
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Times cited : (10)
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References (9)
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