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作 者:任进民[1] 李艳荣[2] 蒋晔[2] 丁翔宇[2] 郝福[2]
机构地区:[1]河北医科大学第二医院药剂科,石家庄050000 [2]河北医科大学药学院,石家庄050017
出 处:《中国现代应用药学》2008年第4期323-325,共3页Chinese Journal of Modern Applied Pharmacy
摘 要:目的建立RP—HPLC-荧光色谱法测定人血浆中盐酸格拉司琼的含量。方法以20名健康男性志愿者为研究对象,采用交叉给药方案,分别单剂量口服2mg的试验制剂和参比制剂。采取液-液萃取法处理血浆样品,色谱柱为Diamonsil C18(150mm×4.6mm,5μm),流动相为甲醇-0.5%三乙胺水溶液(pH4.0)(46:54),激发和发射波长分别为305nm和360nm,流速为1.0mL·min^-1。结果盐酸格拉司琼在0.078~20.08ng·mL^-1线性关系良好(r=0.9994),最低检测限为1.95×10^2ng·mL^-1,日内RSD〈1.9%,日间RSD〈3.3%,平均提取回收率为85.7%,平均方法回收率为100.0%。结论该方法快速、准确,适用于盐酸格拉司琼的临床药动学研究和血药浓度监测。OBJECTIVE A simple RP-HPLC method with fluorescence detection was established for the determination of granisetron hydrochloride in human plasma. METHODS Twenty healthy volunteers were given a single oral dose of granisetron hydrochloride dispersible tablet or tablet (control) in a randomized crossover study. The samples were extracted by liquid-liquid extraction. A Diamonsil C18column was used with the mobile phase of methanol-0.5% triethylamine( pH 4.0 ) (46:54 ) and the flow rate was 1.0 mL ·min^ -1. The excitation and emission wavelengths of fluorescence detection were 305 nm and 360 nm, respectively. RESULTS The calibration curve was linear in the concentration range of 0. 078 - 20.08 ng · mL^-1 and the detective limit of concentration was 1.95 × 10^-2 ng · mL^-1. The intra-day RSD and inter-day RSD were less than 1.9% and 3.3% ,respectively. The average extraction recovery was 85.7%. The average recovery of the method was 100.0%. CONCLUSION The method is sensitive and accurate for the determination of granisetron hydrochloride in human plasma.
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