Identification of unknown impurities in simvastatin substance and tablets by liquid chromatography/tandem mass spectrometry |
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Authors: | Vuletić Marko Cindrić Mario Koruznjak Jasna Dogan |
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Affiliation: | 1. Institute of Photonics, University of Eastern Finland, P.O. Box 111, FI-80101 Joensuu, Finland;2. Department of Chemistry, University of Eastern Finland, P.O. Box 111, FI-80101 Joensuu, Finland;1. Department of Chemistry, Faculty of Arts and Science, Bülent Ecevit University, 67100 Zonguldak, Turkey;2. Department of Chemistry, Faculty of Arts and Science, Düzce University, 81620 Düzce, Turkey;3. Department of Advanced Materials Chemistry, Graduate School of Engineering, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama 240-8501, Japan |
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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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