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作 者:姚秋萍[1,2] 俞道进[3] 李健[3] 马玉芳[3] 黄一帆[3]
机构地区:[1]福建农林大学食品科学学院,福建福州350002 [2]贵州民族学院化学与环境学院,贵州贵阳550019 [3]福建农林大学动物科学学院,福建福州350002
出 处:《福建农林大学学报(自然科学版)》2010年第2期177-180,共4页Journal of Fujian Agriculture and Forestry University:Natural Science Edition
基 金:国家自然科学基金资助项目(30972211)
摘 要:兔的血浆样品经过β-葡萄糖醛酸酶和硫酸酯酶酶解、提取、C18固相萃取小柱富集净化后,在Agilent SB-C18柱(250mm×4.6 mm,5μm)上,以甲醇-0.4%磷酸(55∶45)为流动相,流速为1.0 mL.min-1,检测波长为360 nm,对山奈素进行测定的结果表明,血浆样品的最佳酶解条件为:β-葡萄糖醛酸酶和硫酸酯酶的终用量分别为400和20 U.mL-1,酶解时间为2h;血浆中山奈素含量的线性范围为0.019-0.608μg.mL-1,方法回收率为80.23%-84.27%,日内和日间精密度的RSD分别≤7.32%、10.17%.可见,本试验建立的高效液相色谱测定方法可以准确、灵敏地测定兔血浆中山奈素的含量,适用于山奈素血药含量检测和药代动力学研究.This thesis developed a solid phase extraction-high performance liquid chromatography(SPE-HPLC) method for the determination of Kaempferol in rabbit plasma.In the method,β-Glucuronidase and sulfatase were used to hydrolyze plasma samples before analysis,and Kaempferol in plasma was extracted with a octadecylsilyl C18 SPE column.The mobile phase was methanol.0.4% phosphoric acid(55∶45) with the flow rate of 1 mL·min^-1,and the detection wavelength was set at 360 nm.The results showed that the optimum enzymatic hydrolysis conditions were β-Glucuronidase concentration 400 U·mL^-1,and sulfatase concentration 20 U·mL^-1 for 2 h respectively,the calibration curves for Kaempferol in plasma were liner between 0.019-0.608 g·mL^-1;the assay recovery was 80.23% to 84.27%;the intra-day and inter-day precisions(RSD) were all less than 10.17%.It could be concluded this method had good sensitivity and precision for the determination of Kaempferol in plasma.It was shown to be for pharmacokinetics studies of Kaempferol.
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