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液相色谱-电喷雾电离-串联质谱法同时测定大鼠口服麝香保心丸后血浆中七种蟾毒配基:在药代动力学研究中的应用

Simultaneous determination of seven bufadienolides in rat plasma after oral administration of Shexiang Baoxin Pill by liquid chromatography-electrospray ionization-tandem mass spectrometry: application to a pharmacokinetic study.

作者信息

Wang Shuping, Peng Chengcheng, Jiang Peng, Fu Peng, Tao Jianfei, Han Lin, Huang Huimei, Chang Wanlin, Li Le, Zhang Weidong, Liu Runhui

机构信息

School of Pharmacy, Second Military Medical University, Shanghai 200433, PR China; Department of Pharmacy, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200001, PR China.

School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Sep 15;967:255-63. doi: 10.1016/j.jchromb.2014.07.038. Epub 2014 Aug 4.

Abstract

A liquid chromatography-electrospray ionization-tandem mass spectrometry method was described for the simultaneous determination of resibufogenin, bufalin, gamabufotalin, telibufagin, arenobufagin, cinobufagin and bufotalin in rat plasma. Plasma samples were pretreated by liquid-liquid extraction with ethyl acetate. Chromatographic separation was carried out on an ACQUITY HSS T3 column with gradient elution using mobile phase consisting of acetonitrile-0.1% formic acid in water at a flow rate of 0.3 mL/min. All analytes showed good linearity over a wide concentration range (r>0.99). The lower limit of quantification was in the range of 0.5-10 ng/mL for seven bufadienolides. The mean recovery of the analytes ranged from 94.36 to 104.18%. The intra- and inter-day precisions were in the range of 1.74-13.78% and the accuracies were between 89.37 and 101.38%. The validated method was successfully applied to a pharmacokinetic (PK) study of the seven bufadienolides in rat plasma after oral administration of Shexiang Baoxin Pill (SBP). The selected PK marker compounds with typical efficacy/toxicity may provide a practical solution for marker compound selection and dosage design for the therapeutic drug monitoring and PK study of SBP in its clinical applications.

摘要

建立了一种液相色谱-电喷雾电离-串联质谱法,用于同时测定大鼠血浆中脂蟾毒配基、蟾毒灵、γ-蟾毒它灵、远华蟾毒精、华蟾酥毒基、 cinobufagin和蟾酥灵。血浆样品采用乙酸乙酯液-液萃取法进行预处理。色谱分离在ACQUITY HSS T3柱上进行,采用梯度洗脱,流动相由乙腈-0.1%甲酸水溶液组成,流速为0.3 mL/min。所有分析物在较宽的浓度范围内均表现出良好的线性关系(r>0.99)。7种蟾毒二烯内酯的定量下限在0.5-10 ng/mL范围内。分析物的平均回收率在94.36%至104.18%之间。日内和日间精密度在1.74%-13.78%范围内,准确度在89.37%至101.38%之间。该验证方法成功应用于大鼠口服麝香保心丸(SBP)后血浆中7种蟾毒二烯内酯的药代动力学(PK)研究。所选择的具有典型疗效/毒性的PK标记化合物可为SBP临床应用中的治疗药物监测和PK研究的标记化合物选择和剂量设计提供实用的解决方案。

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