DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING UPLC METHOD FOR ROSUVASTATIN AND ITS RELATED IMPURITIES IN PHARMACEUTICAL DOSAGE FORMS

Title
DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING UPLC METHOD FOR ROSUVASTATIN AND ITS RELATED IMPURITIES IN PHARMACEUTICAL DOSAGE FORMS
Author(s)
박정학G.Venkat Ram Reddy[G.Venkat Ram Reddy]B.Venkateswara Reddy[B.Venkateswara Reddy]Wasimul Haque[Wasimul Haque]Dutt Gautam[Dutt Gautam]Poonam Kumar[Poonam Kumar]프라빈쿠마르
Keywords
MASS-SPECTROMETRY; SPECTROPHOTOMETRIC DETERMINATION; LIQUID-CHROMATOGRAPHY; HUMAN PLASMA; PHARMACOKINETICS; ITRACONAZOLE; PESTICIDES; INHIBITOR; CALCIUM
Issue Date
201102
Publisher
SOC BRASILEIRA QUIMICA
Citation
QUIMICA NOVA, v.34, no.2, pp.250 - 255
Abstract
The present work describes a novel stability-indicating reversed-phase ultra performance liquid chromatography method for the separation and quantification of rosuvastatin (RSV) and its related impurities in the pharmaceutical dosage forms under forced degradation conditions. An unknown degradation impurity detected in the acid degradation was identified by using quadrupole time-of-flight mass spectrometry. The chromatographic separation was carried out on C-18 column (100 x 2.1 mm, 1.7 mu m) using isocratic elution with methanol and 0.1% trifluoroacetic acid (50: 50). The total run time was 12 min within which RSV as well as all related impurities and degradation products were separated. The developed method was validated for RSV and related impurities in pharmaceutical dosage forms.
URI
http://hdl.handle.net/YU.REPOSITORY/25693http://dx.doi.org/10.1590/S0100-40422011000200015
ISSN
0100-4042
Appears in Collections:
이과대학 > 화학생화학부 > Articles
문과대학 > 중국언어문화학과 > Articles
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