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首页> 外文期刊>Analytical and bioanalytical chemistry >Simultaneous determination of harpagoside and cinnamic acid in rat plasma by high-performance liquid chromatography: application to a pharmacokinetic study
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Simultaneous determination of harpagoside and cinnamic acid in rat plasma by high-performance liquid chromatography: application to a pharmacokinetic study

机译:高效液相色谱法同时测定大鼠血浆中的原药甙和肉桂酸:在药代动力学研究中的应用

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摘要

Radix Scrophulariae (Xuanshen) is one of the famous Chinese herbal medicines widely used to treat rheumatism, tussis, pharyngalgia, arthritis, constipation, and conjunctival congestion. Harpagoside and cinnamic acid are the main bioactive components of Xuanshen. The purpose of this study was to develop an HPLC-UV method for simultaneous determination of harpagoside and cinnamic acid in rat plasma and investigate pharmacokinetic parameters of harpagoside and cinnamic acid after oral administration of Xuanshen extract (760 mg kg(-1)). After addition of syringin as internal standard, the analytes were isolated from plasma by liquid-liquid extraction. Separation was achieved on a Kromasil C-18 column, and detection was by UV absorption at 272 nm. The described assay was validated in terms of linearity, accuracy, precision, recovery, and limit of quantification according to the FDA validation guidelines. Calibration curves for both analytes were linear with the coefficient of variation (r) for both was greater than 0.999. Accuracy for harpagoside and cinnamic acid ranged from 100.7-103.5% and 96.9-102.9%, respectively, and precision for both analytes were less than 8.5%. The main pharmacokinetic parameters found for harpagoside and cinnamic acid after oral infusion of Xuanshen extract were as follows: C-max 1488.7 +/- 205.9 and 556.8 +/- 94.2 ng mL(-1), T-max 2.09 +/- 0.31 and 1.48 +/- 0.14 h, AUC(0-24) 10336.4 +/- 1426.8 and 3653.1 +/- 456.4 ng h mL(-1), 456.4 ng h mL(-1), AUC(0-infinity) 111276.8 +/- 1321.4 and 3704.5 +/- 398.8 ng h mL(-1), and t(1/2) 4.9 +/- 1.3 and 2.5 +/- 0.9 h, respectively. These results indicated that the proposed method is simple, selective, and feasible for pharmacokinetic study of Radix Scrophulariae extract in rats.
机译:玄参(Shenph crophulariae,玄参)是著名的中草药之一,广泛用于治疗风湿病,咳嗽,咽痛,关节炎,便秘和结膜充血。人参皂苷和肉桂酸是宣神的主要生物活性成分。这项研究的目的是开发一种同时测定大鼠血浆中哈巴糖苷和肉桂酸含量的HPLC-UV方法,并研究口服玄参提取物(760 mg kg(-1))后哈巴糖苷和肉桂酸的药代动力学参数。加入丁香香精油作为内标后,通过液-液萃取从血浆中分离出分析物。在Kromasil C-18色谱柱上完成分离,并通过272 nm的紫外线吸收进行检测。根据FDA验证指南,在线性,准确性,精密度,回收率和定量限方面验证了所描述的测定方法。两种分析物的校准曲线均呈线性,且两者的变异系数(r)均大于0.999。罗汉果苷和肉桂酸的准确度分别为100.7-103.5%和96.9-102.9%,两种分析物的准确度均低于8.5%。口服口服玄参提取物后发现的原药甙和肉桂酸的主要药动学参数如下:C-max 1488.7 +/- 205.9和556.8 +/- 94.2 ng mL(-1),T-max 2.09 +/- 0.31和1.48 +/- 0.14 h,AUC(0-24)10336.4 +/- 1426.8和3653.1 +/- 456.4 ng h mL(-1),456.4 ng h mL(-1),AUC(0-无穷大)111276.8 + / -1321.4和3704.5 +/- 398.8 ng h mL(-1),以及t(1/2)4.9 +/- 1.3和2.5 +/- 0.9 h。这些结果表明,所提出的方法对于玄参提取物在大鼠体内的药代动力学研究简单,选择性,可行。

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