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采用 UPLC-ESI-MS/MS 法同时测定狗血浆中四种生物活性类黄酮的浓度及其在药代动力学研究中的应用。

Simultaneous determination of four bioactive flavonoids from Polygonum orientale L. in dog plasma by UPLC-ESI-MS/MS and application of the technique to pharmacokinetic studies.

机构信息

Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji School of Pharmacy, Huazhong University of Science and Technology, 13 Hangkong Road, Wuhan 430030, PR China.

Provincial Key Laboratory of Pharmaceutics in Guizhou Province, School of Pharmacy, Guiyang Medical University, 9 Beijing Road, Guiyang 550004, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Apr 15;957:96-104. doi: 10.1016/j.jchromb.2014.02.055. Epub 2014 Mar 12.

Abstract

The in vivo effects of traditional herbal medicines are generally mediated by multiple bioactive components. The main constituents of Polygonum orientale L. are flavonoids such as orientin, vitexin, cynaroside, and quercitrin. The aim of this study was to develop and validate a method for characterizing these flavonoids, in order to better understand the pharmacokinetics and pharmacodynamics of P. orientale L. We used ultra-performance liquid chromatography-electrospray ionization-tandem mass spectrometry (UPLC-ESI-MS/MS) to analyze the flavonoids. After precipitation of the proteins with methanol, the flavonoids were separated on a BEH C18 column (50mm×2.1mm, i.d., 1.7μm) by using an elution gradient of acetonitrile. Flavonoid content was determined using the multiple reaction monitoring (MRM) mode at m/z 449.2→329.2 for orientin, m/z 433.2→313.0 for vitexin, m/z 449.2→287.1 for cynaroside, m/z 449.2→303.4 for quercitrin, and m/z 417.0→267.0 for the internal standard, puerarin. Pharmacokinetics was assessed after intravenous administration of P. orientale L. extracts (POE) in Beagle dogs at a dose of 22, 44, or 88mg/kg. Analysis of the standard curves by linear regression revealed high linearity over a 243-fold dynamic range for the four flavonoids (the lower limit of quantitation values were 4-21ng/mL). The relative standard deviations of intra- and inter-day measurements were less than 15.1%, and the method was accurate to within -8.7% to 7.2%; the extraction recoveries from dog plasma were 70.6-89.3%, 69.8-88.7%, 72.5-85.7%, and 71.0-79.1% for orientin, vitexin, cynaroside, and quercitrin, respectively. Our results suggest non-linear pharmacokinetic characteristics with rapid clearance of the flavonoids. In conclusion, UPLC-ESI-MS/MS is a rapid and sensitive method for simultaneous quantification of multiple flavonoids from POE in dog plasma and is suitable for pharmacokinetic studies of herbal medicines.

摘要

本研究旨在开发和验证一种用于鉴定这些黄酮类化合物的方法,以更好地了解东方蓼的药代动力学和药效学。我们使用超高效液相色谱-电喷雾电离串联质谱法(UPLC-ESI-MS/MS)分析了这些黄酮类化合物。用甲醇沉淀蛋白后,在 BEH C18 柱(50mm×2.1mm,内径,1.7μm)上用乙腈洗脱梯度分离黄酮类化合物。使用多反应监测(MRM)模式,以 m/z 449.2→329.2 测定Orientin、m/z 433.2→313.0 测定 Vitexin、m/z 449.2→287.1 测定 Cynaroside、m/z 449.2→303.4 测定 Quercitrin,以 m/z 417.0→267.0 为内标测定葛根素。以 22、44 或 88mg/kg 的剂量静脉给予东方蓼提取物(POE)后,在比格犬中评估药代动力学。通过线性回归分析标准曲线,四种黄酮类化合物的线性范围为 243 倍(定量下限值为 4-21ng/mL)。日内和日间测量的相对标准偏差均小于 15.1%,方法准确,偏差为-8.7%至 7.2%;从犬血浆中提取的Orientin、Vitexin、Cynaroside 和 Quercitrin 的回收率分别为 70.6-89.3%、69.8-88.7%、72.5-85.7%和 71.0-79.1%。我们的结果表明,黄酮类化合物具有快速清除的非线性药代动力学特征。综上所述,UPLC-ESI-MS/MS 是一种快速灵敏的方法,可用于同时定量检测犬血浆中 POE 的多种黄酮类化合物,适用于草药的药代动力学研究。

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