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作 者:陈镇生[1]
机构地区:[1]浙江省药品检验所
出 处:《药物分析杂志》1999年第2期111-114,共4页Chinese Journal of Pharmaceutical Analysis
摘 要:目的:建立三羟乙基芦丁的血药浓度测定方法。方法:将三羟乙基芦丁转变成四羟乙基芦丁,经高效液相色谱分离后,用荧光检测器测定。结果:血药浓度标准曲线在125~40ng·mL-1间,r=09994;最低检测限为1ng·mL-1;高、中、低3种浓度平均回收率为9152%~9583%。日内和日间平均RSD小于43%和52%。结论:本法可为羟乙基芦丁的药动学研究提供一检测方法。Objective: To establish HPLC method for determining troxerutin in human plasma. Method: Trihydroxyethyl rutoside was converted to tetrahydroxyethyl rutoside by 2-chlorethanol.then separated and determined by HPLC/fluorescence detection. Results: The linear range was between 12540 ngmL-1 with r=09994,and the lowest limit of detection was 1 ngmL-1.The average recovery within the above range was 9152 %9583 %.The RSD values of intraday and interday were lower than 43 % and 52 %,respectively. Conclusion: The present study provides a reliable quantitative method for pharmacokinetic studies of troxerutin.
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