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作 者:赵晓华[1] 宋波[2] 钟大放[2] 张淑秋[1] 陈笑艳[2]
机构地区:[1]山西医科大学,山西太原030001 [2]中国科学院上海药物研究所,上海201203
出 处:《药学学报》2007年第10期1087-1091,共5页Acta Pharmaceutica Sinica
摘 要:建立了快速、灵敏的液相色谱-串联质谱法测定人血浆中的二甲双胍和格列吡嗪.血浆样品经0.3%甲酸-乙腈(v/v)沉淀蛋白后,以乙腈-水-甲酸(70:30:0.3,v/v/v)为流动相,流速为0.50 mL·min^-1.Zorbax Extend C18柱分离,采用大气压化学电离源;以选择反应监测(SRM)方式进行正离子检测.用于定量分析的离子反应分别为m/z 130→m/z 60(二甲双胍),m/z 446→m/321(格列吡嗪)和m/z 256→m/z 167(内标,苯海拉明).测定血浆中二甲双胍的线性范围为2.00~2 000 ng·mL^-1,定量下限为2.00 ng·mL^-1;格列吡嗪的线性范围为1.00~1 000ng·mL^-1,定量下限为1.00 ng·mL^-1.该方法专属性好,灵敏度高,准确快捷,适用于二甲双胍和格列吡嗪的临床药代动力学研究.To develop a sensitive and rapid liquid chromatographic-tandem mass spectrometric (LC-MS/MS) method for simultaneous quantitation of metformin and glipizide in human plasma, metformin, glipizide and internal standard diphenhydramine were separated from plasma by protein precipitation with acetonitrile (containing 0. 3% formic acid), then chromatographed by using a Zorbax Extend C18 column. The mobile phase consisted of acetonitrile-water-formic acid (70: 30: 0.3, v/v/v) , at a flow rate of 0.50 mL . min^-1. A tandem mass spectrometer equipped with atmospheric pressure chemical ionization source was used as detector and operated in the positive ion mode. Selected reaction monitoring (SRM) using the precursor/production combinations of m/z 130→m/z 60, m/z 446→m/z 321 and m/z 256→m/z 167 were used to quantify metformin, glipizide and diphenhydramine, respectively. The linear concentration ranges of the calibration curves for metformin and glipizide were 2. 00 - 2 000 ng . mL^-1 and 1.00 - 1 000 ng . mL^-1, respectively. The lower limits of quantitation of metformin and glipizide were 2.00 ng . mL^- 1 and 1.00 ng . mL^-1, respectively. The method proved to be sensitive, simple and rapid, and suitable for clinical investigation of compound preparation containing metformin and glipizide.
关 键 词:二甲双胍 格列吡嗪 液相色谱-串联质谱法 血浆药物浓度
分 类 号:R917[医药卫生—药物分析学] R969[医药卫生—药学]
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