LC-MS/MS法测定大鼠血浆内尼可地尔浓度及其药动学研究  

Determination of nicorandil in rat plasma by LC-MS/MS method and its pharmacokinetics

作　　者：冯有恒 汪庆 秦燕[1] FENG You-heng;WANG Qing;QIN Yan(State Key Lab of New Drug and Pharmaceutical Process/Shanghai Professional and Technical Service Center for Biological Material Druggability Evaluation,Shanghai Institute of Pharmaceutical Industry,China State Institute of Pharmaceutical Industry,Shanghai 200437,China)

机构地区：[1]中国医药工业研究总院上海医药工业研究院,创新药物与制药工艺国家重点实验室/上海市生物物质成药性评价专业技术服务平台,上海200437

出　　处：《药物分析杂志》2020年第2期240-245,共6页Chinese Journal of Pharmaceutical Analysis

摘　　要：目的:建立LC-MS/MS法测定尼可地尔在大鼠血浆中的浓度,并初步研究其在大鼠体内的药动学行为。方法:血浆样品以甲醇沉淀,采用Kromasil 100-5-C18(2.1 mm×150 mm,5.0μm)色谱柱进行色谱分离。以甲醇-含甲酸铵和甲酸的水溶液为流动相,流速0.3 mL·min-1,进样量4μL,LC-MS/MS分析,分别以m/z 212.1→136.0和m/z 271.2→172.2为尼可地尔和内标(甲苯磺丁脲)的质谱检测条件。大鼠灌服10 mg·kg-1尼可地尔后,不同时间点取样测定其血浆中尼可地尔的浓度。由DAS 2.0计算药动学参数。结果:尼可地尔质量浓度在5.0~2 000.0 ng·mL-1内线性关系良好(r=0.997 9,权重1/X2);定量下限为5.0 ng·mL-1;尼可地尔和内标的提取回收率均高于95%,日内、日间的RSD均小于15%;尼可地尔血浆样品在室温放置4 h,-70℃冰箱放置15 d以及预处理后室温放置24 h的变化率均小于15%。大鼠口服灌胃尼可地尔(10 mg·kg-1)后,尼可地尔在大鼠体内吸收较快,达峰时间约为0.3 h,达峰浓度约为15.0μg·m L-1。结论:建立的LC-MS/MS方法适合于尼可地尔的药动学研究。Objective:To establish a rapid and accurate method of LC-MS/MS determinates nicorandil concentration in rat plasma and to study its pharmacokinetics in rats. Methods:The plasma samples were precipitated with methanol and used the Kromasil 100-5-C18(2.1 mm×150 mm,5.0 μm) chromatographic column to separate nicorandil. The column temperature was 30 ℃. Methanol-the ammonium formate and formic acid aqueous solution was used as the mobile phase. The flow rate was 0.3 mL·min-1 and sample volume was 4 μL. The detection conditions of nicorandil and internal standard(tolbutamide) by mass spectrometry were m/z 212.1-136.0 and m/z 271.2-136.0. Rats were given 10 mg·kg-1 nicorandil by oral gavage and the plasma concentration of nicorandil was detected at different time points. Pharmacokinetic parameters were calculated by DAS 2.0 software. Results:The concentration of nicorandil had a good linear relationship between 5.0 and 2 000.0 ng·ml-1(r=0.997 9,weights 1/X2). The quantitative lower limit was 5.0 ng·mL-1. The extraction recovery of nicorandil and internal standard were higher than 95% and the RSDs of intra day and inter day were less than 15%. Nicorandil plasma samples were placed at room temperature for 4 h and refrigerated at-70 ℃ for 15 days. Finally,the pretreatments and the rates of change are not less than 15% at room temperature for 24 h. After oral intragastric administration of nicodil(10 mg· kg-1)to rats,the pharmacokinetic results showed that the peak time of nicodil in rats was about 0.3 h and the peak concentration was about 15.0 μg· mL-1.Conclusion:The established LC-MS/MS method is suitable for studying the pharmacokinetic of nicorandil.

关 键 词：尼可地尔 抗心绞痛药物 钾通道开放剂 大鼠血浆 血药浓度 药物代谢动力学 高效液相色谱-串联质谱法 

分 类 号：R917[医药卫生—药物分析学]