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采用液相色谱-串联质谱法同时测定枳实提取物中柚皮苷、橙皮苷、新橙皮苷、柚皮素和橙皮素在大鼠血浆中的浓度。

Simultaneous determination of naringin, hesperidin, neohesperidin, naringenin and hesperetin of Fractus aurantii extract in rat plasma by liquid chromatography tandem mass spectrometry.

机构信息

School of Pharmacy, Shenyang Pharmaceutical University, Wenhua Road 103, Shenyang 110016, China.

出版信息

J Pharm Biomed Anal. 2012 Jan 25;58:58-64. doi: 10.1016/j.jpba.2011.05.001. Epub 2011 May 11.

Abstract

A liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed for the simultaneous determination of naringin, hesperidin, neohesperidin, naringenin and hesperetin in rat plasma, using liquiritin as the internal standard. Plasma samples extracted with a solid-phase extraction procedure were separated on a Zorbax SB-C18 analytical column (2.1 mm × 150 mm, 5 μm) and detected by electrospray ionization (ESI) in multiple reaction monitoring (MRM) mode. The calibration curves were linear over the range of 3.0-600 ng/ml for naringin, 0.5-100 ng/ml for hesperidin, 3.5-700 ng/ml for neohesperidin, 5.0-1000 ng/ml for naringenin and hesperetin, respectively. The lower limits of quantification were 0.5 ng/ml for naringin, hesperidin, naringenin and hesperetin, and 0.35 ng/ml for neohesperidin. Intra- and inter-day precision (RSD%) was less than 15% and accuracy (RE%) ranged from -3.3% to 4.8%. The validated method was successfully applied to investigate the pharmacokinetics of the major flavanones of Fructus aurantii extract after oral administration to rats.

摘要

建立了一种同时测定大鼠血浆中柚皮苷、橙皮苷、新橙皮苷、柚皮素和橙皮素的液相色谱-串联质谱(LC-MS/MS)分析方法,以甘草素为内标。采用固相萃取法提取血浆样品,在 Zorbax SB-C18 分析柱(2.1mm×150mm,5μm)上进行分离,采用电喷雾电离(ESI)在多反应监测(MRM)模式下进行检测。柚皮苷、橙皮苷、新橙皮苷、柚皮素和橙皮素的校准曲线在 3.0-600ng/ml、0.5-100ng/ml、3.5-700ng/ml、5.0-1000ng/ml 范围内呈线性。柚皮苷、橙皮苷、柚皮素和橙皮素的定量下限均为 0.5ng/ml,新橙皮苷的定量下限为 0.35ng/ml。日内和日间精密度(RSD%)均小于 15%,准确度(RE%)在-3.3%至 4.8%之间。该方法已成功应用于研究大鼠口服枳实提取物后主要类黄酮的药代动力学。

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