Low level determinations of methyl methanesulfonate and ethyl methanesulfonate impurities in emtricitabine active pharmaceutical ingredient by LC/MS/MS using electrospray ionization.

Analytical Chemistry Insights Pub Date : 2011-01-01 Epub Date: 2011-03-10 DOI:10.4137/ACI.S6471
P R Kakadiya, T G Chandrashekhar, S Ganguly, D K Singh, V Singh
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Abstract

Alkyl methanesulfonates have been highlighted as potential genotoxic impurities (PGIs). A sensitive LC/MS/MS method was developed and validated for the determination of Alkyl methanesulfonate impurities in Emtricitabine API (active pharmaceutical ingredient). LC/MS/MS method on Zorbax SB C(18) column (150 × 4.6 mm i.d.), 3.5 μm, with electrospray ionization (ESI) in multiple reaction monitoring (MRM) mode was used. The proposed method was specific, linear, accurate, rugged and precise. The calibration curves showed good linearity over the concentration range of 0.0025 μg/ml to 0.3 μg/ml the correlation coefficient was >0.999 in each case. Method had very low limit of detection (LOD) and limit of quantification (LOQ) as 0.3 μg/g and 0.4 μg/g respectively for both the analytes. Accuracy was observed within 80%-120% for both the analytes. This method can be further extended a good quality control tool for low level quantitation of Alkyl methanesulfonate impurities in other API.

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利用电喷雾离子化技术,通过 LC/MS/MS 低水平测定恩曲他滨活性药物成分中的甲基磺酸甲酯和甲基磺酸乙酯杂质。
烷基甲烷磺酸盐被认为是潜在的基因毒性杂质(PGIs)。本研究开发并验证了一种灵敏的 LC/MS/MS 方法,用于测定恩曲他滨原料药(活性药物成分)中的甲磺酸烷基酯杂质。采用 Zorbax SB C(18)色谱柱(150 × 4.6 mm i.d.),3.5 μm,电喷雾离子源(ESI),多反应监测(MRM)模式下进行 LC/MS/MS 分析。所提议的方法特异、线性、准确、耐用且精确。在 0.0025 μg/ml 至 0.3 μg/ml 的浓度范围内,线性关系良好,相关系数均大于 0.999。该方法对两种分析物的检出限(LOD)和定量限(LOQ)都很低,分别为 0.3 μg/g 和 0.4 μg/g。两种分析物的准确度均在 80%-120% 之间。该方法可进一步扩展为一种良好的质量控制工具,用于其他原料药中甲磺酸烷基酯杂质的低水平定量分析。
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