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建立一种液相色谱-串联质谱(LC-MS/MS)法,用于同时测定大鼠口服 Protandim 后血浆和不同组织中表没食子儿茶素没食子酸酯、水飞蓟素和姜黄素的浓度,并将其应用于药代动力学和组织分布研究。

Development of a liquid chromatography-tandem mass spectrometric (LC-MS/MS) method for simultaneous determination of epigallocatechin-3-gallate, silibinin, and curcumin in plasma and different tissues after oral dosing of Protandim in rats and its application in pharmacokinetic and tissue distribution studies.

机构信息

Department of Pharmacy, Xijing Hospital, Air Force Military Medical University, Xi'an, Shaanxi, PR China; School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, Shaanxi, PR China.

The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, PR China.

出版信息

J Pharm Biomed Anal. 2019 Jun 5;170:54-62. doi: 10.1016/j.jpba.2019.03.024. Epub 2019 Mar 14.

Abstract

Protandim is an over-the-counter herbal dietary supplement. The key components of Protandim, i.e., epigallocatechin-3-gallate (EGCG), silibinin (SIL), and curcumin (CUR) were simultaneously analyzed through a liquid chromatography-tandem mass spectrometric (LC-MS/MS) method in plasma and different tissues after administration of Protandim in rats. The developed and validated method was employed to assess the pharmacokinetic profiles and the accumulation of EGCG, SIL, CUR in rat plasma and tissue homogenates. The plasma and tissue homogenates were subjected to liquid-liquid extraction and separated on a Hypurity C18 column (50 × 4.6 mm) with a gradient elution of water and acetonitrile. Mass spectrometric detection was performed in the multiple reaction monitoring mode (MRM) following the transitions: m/z 457.3/169.3, m/z 481.3/125.0, m/z 367.3/149.3 and m/z 609.4 /300.2 for EGCG, SIL, CUR, and RU (rutin), respectively. The concentrations of all the analytes in the range from 2 to 1000 ng/mL showed linear relationships with respective peak areas in different matrices. For all matrices, the values of inter-day and intra-day precisions and accuracies were less than 10.3% of the nominal concentration. The matrix effect, extraction recovery, dilution integrity, and stability values were all within acceptable levels. This method was successfully applied for determining the pharmacokinetics and tissue distribution of the components in rats after the intragastrical administration of a single-dose (364.5 mg/kg) or multiple-doses (1458 mg/kg) of Protandim. The data showed that EGCG, SIL, and CUR did not accumulate in rats after multiple doses of Protandim, and the three main components were distributed mainly in the small intestine.

摘要

Protandim 是一种非处方草本膳食补充剂。采用液相色谱-串联质谱(LC-MS/MS)法同时分析 Protandim 给药后大鼠血浆和不同组织中的关键成分,即表没食子儿茶素没食子酸酯(EGCG)、水飞蓟宾(SIL)和姜黄素(CUR)。建立并验证了该方法,用于评估 EGCG、SIL、CUR 在大鼠血浆和组织匀浆中的药代动力学特征和蓄积情况。将血浆和组织匀浆进行液-液萃取,在 Hypurity C18 柱(50×4.6mm)上进行梯度洗脱,以水和乙腈为洗脱液。采用多反应监测模式(MRM)进行质谱检测,转换为:m/z 457.3/169.3、m/z 481.3/125.0、m/z 367.3/149.3 和 m/z 609.4/300.2,用于 EGCG、SIL、CUR 和 RU(芦丁)。所有分析物在 2-1000ng/mL 范围内的浓度与不同基质中的相应峰面积均呈线性关系。对于所有基质,日内和日间精密度和准确度的测定值均小于标称浓度的 10.3%。基质效应、提取回收率、稀释完整性和稳定性值均在可接受范围内。该方法成功应用于单次(364.5mg/kg)或多次(1458mg/kg)灌胃给予 Protandim 后大鼠体内各成分的药代动力学和组织分布研究。结果表明,多次给予 Protandim 后,EGCG、SIL 和 CUR 并未在大鼠体内蓄积,三种主要成分主要分布在小肠中。

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