利用 LC-MS/MS 对盐酸伊伐布雷定中的潜在基因毒性杂质 Veratryl Chloride 进行室内毒性评估和痕量定量

Rajavenkata P Patha, Karunakar Dasa, R. Bhoomireddy, Srinivas R Thumu
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摘要

为痕量分析盐酸伊伐布雷定(IVB)中潜在的基因毒性杂质--4-(氯甲基)-1, 2-二甲氧基苯(Veratryl chloride),开发并验证了一种采用多反应监测(MRM)模式的灵敏、选择性液相色谱-质谱(LC-MS/MS)分析方法。色谱分离采用 Poroshell 120EC C18(50 × 3.0 mm,2.7 μm)色谱柱,使用 10 mM 甲酸铵和乙腈的混合物,以 0.25 mL/min 的流速在等度洗脱模式下进行。柱前用二乙胺进行了简单的衍生化处理。所建立的 LC-MS/MS 方法在 1.5-10.0 ppm 浓度范围内线性关系良好,r2 ˃ 0.999,回收率大于 90%。所开发的方法精确度高,RSD (%) 不超过 4.5%。采用 ICH M7 原则评估了藜芦酰氯的体内遗传毒性和致癌性,结果呈阳性。所开发的方法可鉴定和定量 IVB 中的藜芦酰氯,因此可用于制药行业质量控制实验室的痕量定量分析。
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In-silico Toxicity Assessment and Trace Level Quantification of Veratryl Chloride a Potential Genotoxic Impurity in Ivabradine Hydrochloride using LC-MS/MS
A sensitive and selective liquid chromatography-mass spectrometry (LC-MS/MS) method using multiple reaction monitoring (MRM) mode was developed and validated for trace analysis of 4-(chloromethyl)-1, 2-dimethoxybenzene (Veratryl chloride) a potential genotoxic impurity in Ivabradine hydrochloride (IVB). Chromatographic separation was performed on a Poroshell 120EC C18 (50 × 3.0 mm, 2.7 μm) column using a mixture of 10 mM ammonium formate and acetonitrile in isocratic elution mode at a 0.25 mL/min flow rate. A simple pre-column derivatization with di-ethylamine was employed for the derivatization of the veratryl chloride. The developed LC-MS/MS method was linear and accurate in the 1.5–10.0 ppm concentration range with r2 ˃ 0.999 and percent recoveries greater than 90%. The developed method was precise with RSD (%) of not more than 4.5%. In-silico genotoxicity and carcinogenicity potential of veratryl chloride was assessed using ICH M7 principles found to be positive. The developed method can identify and quantify veratryl chloride in IVB, hence can be applied by quality control labs of pharmaceutical industries for trace quantification.
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