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Method Development and Validation for Pharmacokinetic and Tissue Distributions of Ellagic Acid Using Ultrahigh Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS)

机译:超高效液相色谱-串联质谱法(UPLC-MS / MS)对鞣花酸药代动力学和组织分布的方法开发和验证

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摘要

Ellagic acid is a dietary polyphenol found in numerous fruits and vegetables, possessing several health benefits such as antioxidant, anticancer and anti-atherosclerotic biological properties. The purpose of this study was to explore the pharmacokinetics and tissue distribution of ellagic acid in rats. A simple, rapid, sensitive and specific liquid chromatography–tandem mass spectrometry method to determine the ellagic acid in plasma and tissue samples was developed and validated. The separation was achieved using reversed-phase ultra-performance liquid chromatography (UPLC), and the mass spectrometric detection was achieved using heated electrospray ionization (negative mode) and multiple ion monitoring (m/z 301/229). A sample cleanup with a solid phase extraction (SPE) step prior to the UPLC-MS/MS analysis was also developed. The SPE and UPLC-MS/MS method established here was successfully applied to reveal the pharmacokinetic profiles and tissue distribution of ellagic acid. After oral administration dosing at 50 mg/kg, plasma levels of ellagic acid peaked at about 0.5 h, with Cmax value of 93.6 ng/mL, and the results showed that the ellagic acid was poorly absorbed after oral administration. The pharmacokinetic profile of ellagic acid fitted to a two-compartment model with t1/2α 0.25 h and t1/2β 6.86 h, respectively. Following oral administration, ellagic acid was detected in all examined tissues including kidney, liver, heart, lung and brain et al., and the highest levels were found in kidney and liver.
机译:鞣花酸是一种在多种水果和蔬菜中发现的膳食多酚,具有多种健康益处,例如抗氧化剂,抗癌和抗动脉粥样硬化生物学特性。这项研究的目的是探讨鞣花酸在大鼠体内的药代动力学和组织分布。开发并验证了一种简单,快速,灵敏且特异的液相色谱-串联质谱法测定血浆和组织样品中的鞣花酸。使用反相超高效液相色谱(UPLC)进行分离,并使用加热的电喷雾电离(负模式)和多离子监测(m / z 301/229)进行质谱检测。还开发了在UPLC-MS / MS分析之前通过固相萃取(SPE)步骤进行的样品净化。本文建立的SPE和UPLC-MS / MS方法已成功应用于揭示鞣花酸的药代动力学特征和组织分布。口服给药50 mg / kg后,鞣花酸的血浆水平在约0.5 h达到峰值,Cmax值为93.6 ng / mL,结果表明,口服后鞣花酸的吸收较差。鞣花酸的药代动力学曲线分别适用于t1 /2α0.25 h和t1 /2β6.86 h的两室模型。口服后,在包括肾脏,肝脏,心脏,肺和脑等所有受检组织中均检出鞣花酸,在肾脏和肝脏中检出的鞣花酸含量最高。

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