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高效液相色谱-串联质谱法同时测定大鼠血浆中14-噻吩亚甲基苦参碱和苦参碱及其在药代动力学研究中的应用

Simultaneous determination of 14-thienyl methylene matrine and matrine in rat plasma by high-performance liquid chromatography-tandem mass spectrometry and its application in a pharmacokinetic study.

作者信息

Jiang Minjie, Wang Lisheng, Jiang Weizhe, Huang Shulin

机构信息

School of Chemistry and Chemical Engineering, Guangxi University, 100 Daxue Road, Nanning 530004, China.

School of Chemistry and Chemical Engineering, Guangxi University, 100 Daxue Road, Nanning 530004, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Jan 1;974:126-30. doi: 10.1016/j.jchromb.2014.10.041. Epub 2014 Nov 6.

Abstract

A rapid, sensitive and selective high-performance liquid chromatography-tandem mass spectrometric method (HPLC-MS) has been developed and validated for the simultaneous determination of 14-thienyl methylene matrine (TMM) and matrine (MT) in rat plasma in the present study. The analytes were separated on a C18 column (1.9 μm, 2.1 mm × 100 mm) with a security guard C18 column (5 μm, 2.1 mm × 10 mm) and a triple-quadrupole mass spectrometry equipped with an electrospray ionization (ESI) source was applied for detection. With pseudoephedrine hydrochloride as internal standard, sample pretreatment involved in a one-step protein precipitation with isopropanol:ethyl acetate (v/v, 20:80). The method was linear over the concentration ranges of 5-1000 ng/ml for TMM and 10-2000 ng/ml for MT. The intra-day and inter-day relative standard deviations (RSD) were less than 15% and the relative errors (RE) were all within 15%. The proposed method enables unambiguous identification and quantification of TMM and MT in vivo. This was the first report on determination of the TMM and MT in rat plasma after oral administration of TMM. The results provided a meaningful basis for evaluating the clinical applications of the medicine.

摘要

本研究建立并验证了一种快速、灵敏且选择性高的高效液相色谱-串联质谱法(HPLC-MS),用于同时测定大鼠血浆中的14-噻吩亚甲基苦参碱(TMM)和苦参碱(MT)。分析物在C18柱(1.9μm,2.1mm×100mm)上分离,配备保护柱C18柱(5μm,2.1mm×10mm),并采用配备电喷雾电离(ESI)源的三重四极杆质谱进行检测。以盐酸伪麻黄碱为内标,样品预处理采用异丙醇:乙酸乙酯(v/v,20:80)一步沉淀蛋白法。该方法在TMM浓度范围为5-1000ng/ml、MT浓度范围为10-2000ng/ml内呈线性。日内和日间相对标准偏差(RSD)均小于15%,相对误差(RE)均在15%以内。所建立的方法能够明确鉴定和定量体内的TMM和MT。这是首次关于口服TMM后大鼠血浆中TMM和MT测定的报道。研究结果为评估该药物的临床应用提供了有意义的依据。

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