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建立一种 LC-MS/MS 方法,用于同时测定替格瑞洛及其活性代谢物在与阿托伐他汀合用期间的浓度。

Development of an LC-MS/MS method for simultaneous determination of ticagrelor and its active metabolite during concomitant treatment with atorvastatin.

机构信息

Department of Physical Pharmacy and Pharmacokinetics, Poznan University of Medical Sciences, Święcickiego 6 St, 60-781 Poznań, Poland.

Department of Physical Pharmacy and Pharmacokinetics, Poznan University of Medical Sciences, Święcickiego 6 St, 60-781 Poznań, Poland.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2019 Jan 15;1105:113-119. doi: 10.1016/j.jchromb.2018.12.018. Epub 2018 Dec 16.

Abstract

A combination of antiplatelet drugs with high-intensity statin therapy is a standard in patients with coronary events. Concomitant treatment with ticagrelor, a moderate CYP3A4 inhibitor, and CYP3A4-metabolized statins such as atorvastatin, might lead to an increased risk of muscle-related adverse events. Therefore, investigation of concentrations of these compounds in clinical samples is necessary. For this purpose, an LC-MS/MS method was developed for simultaneous determination of ticagrelor and its active metabolite (AR-C124910XX), as well as 2-hydroxyatorvastatin, which is the main metabolite of atorvastatin. Protein precipitation was used for sample preparation and afterwards the analytes were separated on a Kinetex XB-C18 column with an isocratic elution (water and acetonitrile with 0.1% formic acid, 57:43, v/v). Detection was performed on a triple-quadrupole MS with multiple-reaction-monitoring via electrospray ionization. The method was fully validated according to the EMA's recommendations. Determination was possible within ranges: 1.25-2000 ng/mL for ticagrelor, 1.25-1000 ng/mL for its AR-C124910XX, 1.25-50 ng/mL for atorvastatin and 1.14-45.73 for 2-hydroxyatorvastatin. Within and between-run accuracy, expressed as a relative error, was within 0.05-10.56% for all analytes, while within and between-run precision, expressed as coefficient of variation, was within 0.61-9.91%. Ticagrelor, atorvastatin and their main metabolites were found to be stable in acetonitrile stock solutions, and in plasma samples stored for 24 h at room temperature, 1 month at -25 °C, after 3 cycles of freezing and thawing, and in processed samples stored as a dry residue for 24 h at 4 °C and for 24 h in autosampler at room temperature. This simple and rapid method allowed simultaneous determination of the analytes for the first time. The procedure was applied for the pharmacokinetic study of ticagrelor, its active metabolite AR-C124910XX, and 2-hydroxyatorvastatin in patients simultaneously treated with ticagrelor and atorvastatin.

摘要

联合使用抗血小板药物和高强度他汀类药物治疗是冠心病患者的标准治疗方案。同时使用中等强度 CYP3A4 抑制剂替格瑞洛和 CYP3A4 代谢的他汀类药物,如阿托伐他汀,可能会增加肌肉相关不良反应的风险。因此,有必要在临床样本中检测这些化合物的浓度。为此,开发了一种 LC-MS/MS 方法,用于同时测定替格瑞洛及其活性代谢物(AR-C124910XX)以及阿托伐他汀的主要代谢物 2-羟基阿托伐他汀。样品制备采用蛋白沉淀法,然后在 Kinetex XB-C18 柱上进行等度洗脱(水和乙腈,含 0.1%甲酸,57:43,v/v)。通过电喷雾电离进行三重四极杆 MS 多反应监测检测。该方法完全按照 EMA 的建议进行了验证。测定范围为:替格瑞洛 1.25-2000ng/mL,AR-C124910XX 1.25-1000ng/mL,阿托伐他汀 1.25-50ng/mL,2-羟基阿托伐他汀 1.14-45.73ng/mL。所有分析物的批内和批间准确度,以相对误差表示,均在 0.05-10.56%范围内,而批内和批间精密度,以变异系数表示,均在 0.61-9.91%范围内。替格瑞洛、阿托伐他汀及其主要代谢物在乙腈储备溶液中稳定,在室温下保存 24 小时、-25°C 保存 1 个月、冷冻和解冻 3 个循环后以及在干燥残渣中保存 24 小时和在室温下自动进样器中保存 24 小时的血浆样品中稳定。该方法简单快速,首次实现了同时测定这些分析物。该方法用于同时接受替格瑞洛和阿托伐他汀治疗的患者中替格瑞洛、其活性代谢物 AR-C124910XX 和 2-羟基阿托伐他汀的药代动力学研究。

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