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首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >A simple RP-HPLC method for the simultaneous determination of curcumin and its prodrug, curcumin didecanoate, in rat plasma and the application to pharmacokinetic study.
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A simple RP-HPLC method for the simultaneous determination of curcumin and its prodrug, curcumin didecanoate, in rat plasma and the application to pharmacokinetic study.

机译:一种同时测定大鼠血浆中姜黄素及其前药姜黄素二癸酸酯的简单RP-HPLC方法,并用于药代动力学研究。

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摘要

A high-performance liquid chromatographic (HPLC) method has been developed for the simultaneous determination of curcumin and its prodrug, curcumin didecanoate (CurDD), in rat plasma. The analytes were extracted by ethyl acetate following the addition of sodium dodecyl sulfate, and separated on a reverse-phase C(18) column using a gradient mobile phase system of acetonitrile-tetrahydrofuran-water containing 0.1% formic acid. Detection by UV absorption at 425 nm gave a lower limit of quantitation (LLOQ) of 5 and 10 ng/mL for curcumin and CurDD in 50 muL of plasma, respectively. Intra- and inter-day precisions of quality control samples except those at LLOQ were within 15% for curcumin and CurDD, respectively, and the accuracies for both compounds were between 93.9 and 108%. The method was successfully applied to determine plasma concentration-time curves of curcumin and CurDD in rats following intravenous (i.v.) administration of curcumin or CurDD at doses of 1 mg/kg (calculated as curcumin). The results suggested that i.v. dosed CurDD provided sustained plasma levels of curcumin.
机译:开发了一种高效液相色谱(HPLC)方法,用于同时测定大鼠血浆中的姜黄素及其前药姜黄素二癸酸酯(CurDD)。加入十二烷基硫酸钠后,用乙酸乙酯萃取分析物,并使用含有0.1%甲酸的乙腈-四氢呋喃-水梯度流动相系统在反相C(18)色谱柱上进行分离。通过在425 nm处的紫外线吸收检测,在50μL血浆中姜黄素和CurDD的定量下限(LLOQ)分别为5和10 ng / mL。姜黄素和CurDD的质量控制样品的日内和日间精密度(分别在LLOQ处)均在15%以内,两种化合物的准确度均在93.9至108%之间。在以1 mg / kg剂量(以姜黄素计算)静脉内(i.v.)施用姜黄素或CurDD后,该方法已成功应用于测定姜黄素和CurDD的血浆浓度-时间曲线。结果表明剂量的CurDD可提供持续的姜黄素血浆水平。

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