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作 者:Paraag Gide Sandeep Sonawane Abhishek Chitnis
机构地区:[1]MET's Institute of Pharmacy,MET League of Colleges,Bhujbal Knowledge City,Nashik 422003,Maharashtra,India [2]Department of Clinical Sciences and Administration,University of Houston,College of Pharmacy,Houston,TX 77030,USA
出 处:《Journal of Pharmaceutical Analysis》2012年第5期390-393,共4页药物分析学报(英文版)
摘 要:A rapid and simple high performance liquid chromatography (HPLC) mcthod wiih a UV detection (241 nm) was developed and validated for estimation of eplerenone from spiked human plasma. The analyte and the internal standard (valdecoxib) were extracted with a mixture of dichloromethane and diethyl ether. The chromatographic separation was performed on a HiQSil C-18HS column (250 mm × 4.6 mm, 5 um) with a mobile phase consisting of acetonitrile:water (50:50, v/v) at flow rate of 1 mL/min. The calibration curve was linear in the range 100 3200 ng/mL and the heteroscedasticity was minimized by using weighted least squares regression with weighting factor I/X.A rapid and simple high performance liquid chromatography (HPLC) mcthod wiih a UV detection (241 nm) was developed and validated for estimation of eplerenone from spiked human plasma. The analyte and the internal standard (valdecoxib) were extracted with a mixture of dichloromethane and diethyl ether. The chromatographic separation was performed on a HiQSil C-18HS column (250 mm × 4.6 mm, 5 um) with a mobile phase consisting of acetonitrile:water (50:50, v/v) at flow rate of 1 mL/min. The calibration curve was linear in the range 100 3200 ng/mL and the heteroscedasticity was minimized by using weighted least squares regression with weighting factor I/X.
关 键 词:EPLERENONE Liquid-liquidextraction Weighted regression HPLC-UV
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