首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Development and validation of a highly sensitive LC-MS/MS-ESI method for quantification of IIIM-019-A novel nitroimidazole derivative with promising action against Tuberculosis: Application to drug development
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Development and validation of a highly sensitive LC-MS/MS-ESI method for quantification of IIIM-019-A novel nitroimidazole derivative with promising action against Tuberculosis: Application to drug development

机译:开发和验证一种高灵敏度的LC-MS / MS-ESI方法,用于定量IIIM-019-A具有抗结核作用的新型硝基咪唑衍生物:在药物开发中的应用

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The study aims to illustrate an analytical validation of a rapid and sensitive liquid chromatography (LC) coupled to tandem mass spectrometry (MS-MS) and electrospray ionization (ESI) method for quantification of IIIM-019 (a novel nitroimidazole derivative with potential activity against Tuberculosis) in mice plasma. The extraction of the analyte and the internal standard (Tolbutamide) from the plasma samples involves protein precipitation using acetonitrile. The chromatographic separation was accomplished using a gradient mode and the mobile phase comprised of acetonitrile and 0.1% formic acid in water. The flow rate used was 0.7 ml/min on a C(18)e high performance Chromolith column. IIIM-019 and Tolbutamide (IS) were analyzed by combined reversed-phase LC/MS-MS with positive ion electrospray ionization. The MS-MS ion transitions used were 533 > 170.1, 533 > 198 for IIIM-019 and 271 > 74, 271 > 155 for internal standard (IS) respectively. The method was linear over a concentration range of 0.5-1000 ng/ml and the lower limit of quantification was 0.50 ng/ml. The entire study was validated for accuracy, precision, linearity, range, selectivity, lower limit of quantification (LLOQ), recovery, and matrix effect in accordance with the FDA guidelines of method validation. Acceptable precision and accuracy were obtained for concentrations over the standard curve range. The intra and inter-day precisions were in the range of 0.51-11.18% and 0.51-7.55%. The pharmacokinetics was performed on male Balb/c mice by oral (2.5 mg/kg), intraperitoneal (2.5 mg/kg) and intravenous (1 mg/kg) routes. The oral bioavailability of IIIM-019 was 51.6%. The method was also applied successfully in determining microsomal stability wherein the compound was found to be very slightly metabolized by rat liver microsomes. (C) 2016 Elsevier B.V. All rights reserved.
机译:这项研究旨在说明快速灵敏液相色谱(LC)结合串联质谱(MS-MS)和电喷雾电离(ESI)方法定量分析IIIM-019(对硝基苯甲酰胺具有潜在活性的新型硝基咪唑衍生物)的分析验证结核)在小鼠血浆中。从血浆样品中提取分析物和内标(甲苯磺丁酰胺)涉及使用乙腈进行蛋白质沉淀。色谱分离使用梯度模式完成,流动相由乙腈和0.1%的甲酸水溶液组成。在C(18)e高性能Chromolith色谱柱上使用的流速为0.7 ml / min。通过将反相LC / MS-MS与正离子电喷雾电离相结合来分析IIIM-019和甲苯磺丁酰胺(IS)。对于IIIM-019,所用的MS-MS离子跃迁分别为533> 170.1、533> 198和对于内标(IS)为271> 74、271> 155。该方法在0.5-1000 ng / ml的浓度范围内是线性的,定量下限为0.50 ng / ml。根据FDA方法验证指南,对整个研究的准确性,精密度,线性,范围,选择性,定量下限(LLOQ),回收率和基质效应进行了验证。对于标准曲线范围内的浓度,获得了可接受的精度和准确度。日内和日间精度在0.51-11.18%和0.51-7.55%之间。通过口服(2.5mg / kg),腹膜内(2.5mg / kg)和静脉内(1mg / kg)途径对雄性Balb / c小鼠进行药代动力学。 IIIM-019的口服生物利用度为51.6%。该方法还成功地用于确定微粒体稳定性,其中发现该化合物被大鼠肝微粒体非常轻微地代谢。 (C)2016 Elsevier B.V.保留所有权利。

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