He Hui, Chen Xijing, Wang Guangji, Wang Jiping, Davey Andrew Keith
Center of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing, Jiangsu 210009, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Mar 7;832(2):177-80. doi: 10.1016/j.jchromb.2005.12.021. Epub 2006 Jan 30.
A HPLC method for determination of trans-resveratrol concentrations in rat plasma was developed. Plasma samples were treated with acetonitrile to deposit proteins. The analysis used a Hypersil ODS(2) C(18) column (5 microm, 4.6 mm x 250 mm) and methanol/distilled water as the mobile phase (flow-rate=1 mL/min). The UV detection wavelength was 303 nm, and chlorzoxazone was used as the internal standard. The calibration curve was linear over the range of 0.02-40 microg/mL with a correlation coefficient of 0.9997. This concentration range corresponds well with the plasma concentrations of resveratrol in pharmacokinetic studies. There was 98.7%, 91.3% and 84.4% recovery from 0.02, 0.4 and 40 microg/mL plasma samples respectively. The R.S.D. of intra- and inter-day assay variations were all less than 12%. This HPLC assay is a quick, precise and reliable method for the analysis of resveratrol in pharmacokinetic studies.
建立了一种测定大鼠血浆中反式白藜芦醇浓度的高效液相色谱法。血浆样品用乙腈处理以沉淀蛋白质。分析采用Hypersil ODS(2) C(18) 柱(5微米,4.6毫米×250毫米),以甲醇/蒸馏水为流动相(流速=1毫升/分钟)。紫外检测波长为303纳米,氯唑沙宗用作内标。校准曲线在0.02 - 40微克/毫升范围内呈线性,相关系数为0.9997。该浓度范围与药代动力学研究中白藜芦醇的血浆浓度非常吻合。从0.02、0.4和40微克/毫升血浆样品中的回收率分别为98.7%、91.3%和84.4%。日内和日间测定变异的相对标准偏差均小于12%。这种高效液相色谱法是药代动力学研究中分析白藜芦醇的一种快速、精确且可靠的方法。