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Determination of galangin in rat plasma by UPLC and pharmacokinetic study

机译:超高效液相色谱法和药代动力学研究测定大鼠血浆中高良姜精

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摘要

In this study, a simple, sensitive, and robust analytical method based on ultra-performance liquid chromatography (UPLC) has been developed for the determination of galangin in rat plasma using diazepam as internal standard (IS). After sample preparation by a simple liquid-liquid extraction, chromatography was performed on an Acquity UPLC BEH C18 column (2.1 mm x 50 mm, 1.7 mu m particle size) and ultraviolet detection set at a wavelength of 360 nm. The method was linear over the concentration range 10-1000 ng/mL with a lower limit of quantification (LLOQ) of 10 ng/mL. Inter- and intra-day precision (RSD %) were all within 9.5% and the accuracy (RE %) was equal or lower than 8.9%. Recoveries of galangin and IS were more than 78.3%. Stability studies showed that galangin was stable under a variety of storage conditions. The method was successfully applied to a pharmacokinetic study involving oral administration of galangin to rats. (C) 2015 Elsevier B.V. All rights reserved.
机译:在这项研究中,已经开发了一种基于超高效液相色谱(UPLC)的简单,灵敏且稳定的分析方法,以地西epa为内标(IS)测定大鼠血浆中的高良姜精。通过简单的液-液萃取制备样品后,在Acquity UPLC BEH C18色谱柱(2.1 mm x 50 mm,粒径1.7μm)上进行色谱,并在360 nm波长处进行紫外检测。该方法在10-1000 ng / mL的浓度范围内是线性的,定量下限(LLOQ)为10 ng / mL。日间和日内精度(RSD%)均在9.5%以内,精度(RE%)等于或低于8.9%。高良姜精和IS的回收率均超过78.3%。稳定性研究表明,高良姜精在各种储存条件下均稳定。该方法已成功应用于涉及大鼠高良姜素口服的药代动力学研究。 (C)2015 Elsevier B.V.保留所有权利。

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