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液相色谱-电喷雾电离-串联质谱法测定血浆中丹参酮ⅡA磺酸钠

Determination of sodium tanshinone IIA sulfonate in plasma by liquid chromatography-electrospray ionisation-tandem mass spectrometry.

作者信息

Hao Haiping, Wang Guangji, Cui Nan, Li Jing, Ding Zuoqi

机构信息

Key Laboratory of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, 1 Shennong Road, Nanjing 210038, People's Republic of China.

出版信息

Biomed Chromatogr. 2007 Nov;21(11):1172-9. doi: 10.1002/bmc.871.

Abstract

Sodium tanshinone IIA sulfonate (STS) is a water-soluble derivative of tanshinone IIa, an important lipophilic component contained in Salvia miltiorrhizae. A simple, sensitive and robust quantification method for STS based on LC-ESI-MS/MS was developed and validated, and has been successfully applied to the pharmacokinetic study. Liquid-liquid extraction was used for extracting STS from biological samples, with a satisfactory recovery exceeding 75% at all test concentrations. Isocratic mobile phase consisted of 75% acetonitrile and 25% water containing 0.005% ammonia acetate (pH 3). Good retention and baseline separation for STS and the selected internal standard, diclofenac sodium, were obtained on a Shim-pack VP-ODS analytical column under this condition. The method was linear in the concentration range of 1-500 ng/mL. The intra- and inter-day precisions (RSD%) were within 9.0%. The deviation of the assay accuracies was within +/-10.0%. STS was proved to be stable during all sample storing, preparation and analytic procedures. With a lower limit of quantitation at 1 ng/mL, this method has been proved to be sensitive enough for the pharmacokinetic study of STS. The plasma profile of STS followed a single intravenous dosing was well fitted to a three compartmental model.

摘要

丹参酮IIA磺酸钠(STS)是丹参中重要的亲脂性成分丹参酮IIA的水溶性衍生物。建立并验证了一种基于液相色谱-电喷雾串联质谱(LC-ESI-MS/MS)的简单、灵敏且稳健的STS定量方法,并已成功应用于药代动力学研究。采用液-液萃取法从生物样品中提取STS,在所有测试浓度下回收率均超过75%,结果令人满意。等度流动相由75%乙腈和25%含0.005%醋酸铵(pH 3)的水组成。在此条件下,在Shim-pack VP-ODS分析柱上,STS与选定的内标双氯芬酸钠实现了良好的保留和基线分离。该方法在1-500 ng/mL的浓度范围内呈线性。日内和日间精密度(相对标准偏差%)均在9.0%以内。测定准确度的偏差在+/-10.0%以内。已证明STS在所有样品储存、制备和分析过程中均稳定。该方法的定量下限为1 ng/mL,已证明对STS的药代动力学研究足够灵敏。单次静脉给药后STS的血浆浓度-时间曲线很好地拟合三室模型。

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