Literature DB >> 15797793

Identification of unknown impurities in simvastatin substance and tablets by liquid chromatography/tandem mass spectrometry.

Marko Vuletić1, Mario Cindrić, Jasna Dogan Koruznjak.   

Abstract

Unknown impurities were detected in simvastatin substance and tablets at a 0.2% level using the liquid chromatography technique with UV (DAD) detection. The impurity structures were elucidated by a direct hyphenation of liquid chromatograph to high-resolution mass spectrometer with electrospray ionisation interface using solutions of formic acid in water and in acetonitrile as the mobile phase. Peak tracking was performed using the column-switching technique. Accurate mass measurements by quadrupole time-of-flight mass spectrometer equipped with lock-spray provided information about elemental composition of intact molecules and fragments of impurities. Measurement accuracy for precursor ions was around 3 ppm and for fragment ions between 4 and 13 ppm. Mass resolving power was around 6500. Deduced molecular formulae for A1, A2 and A3 impurities were C(27)H(44)O(6), C(26)H(43)O(6) and C(26)H(41)O(5), respectively. The structures proposed for all three impurities revealed modifications of simvastatin molecule on the lactone ring. Impurity A1, detected in simvastatin tablets, was identified as ethyl ester, while the impurities A2 and A3, detected in simvastatin substance, were identified as methyl ester and methyl ether of simvastatin. The impurity from tablets was synthesized and its structure confirmed by LC-UV, LC-MS/MS, and NMR techniques.

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Year:  2004        PMID: 15797793     DOI: 10.1016/j.jpba.2004.11.047

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  4 in total

1.  Effects of highly hygroscopic excipients on the hydrolysis of simvastatin in tablet at high relative humidity.

Authors:  W L Chen; D W Guo; Y Y Shen; S R Guo; K P Ruan
Journal:  Indian J Pharm Sci       Date:  2012-11       Impact factor: 0.975

2.  Stability Indicating RP-HPLC Method for Simultaneous Determination of Simvastatin and Ezetimibe from Tablet Dosage Form.

Authors:  R P Dixit; C R Barhate; S G Padhye; C L Viswanathan; M S Nagarsenker
Journal:  Indian J Pharm Sci       Date:  2010-03       Impact factor: 0.975

3.  Synthesis, characterization and quantification of simvastatin metabolites and impurities.

Authors:  Manish S Bhatia; Swapnil D Jadhav; Neela M Bhatia; Prafulla B Choudhari; Kundan B Ingale
Journal:  Sci Pharm       Date:  2011-07-25

4.  Comprehensive Assessment of Degradation Behavior of Simvastatin by UHPLC/MS Method, Employing Experimental Design Methodology.

Authors:  Maja Hadzieva Gigovska; Ana Petkovska; Jelena Acevska; Natalija Nakov; Packa Antovska; Sonja Ugarkovic; Aneta Dimitrovska
Journal:  Int J Anal Chem       Date:  2018-08-08       Impact factor: 1.885

  4 in total

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