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作 者:丁翔宇[1] 蒋晔[1] 安普丽[1] 郝福[1] 李艳荣[1]
出 处:《中国药房》2007年第14期1076-1078,共3页China Pharmacy
摘 要:目的:建立以反相高效液相色谱法测定人血浆中盐酸特拉唑嗪浓度的方法。方法:血样采用二氯甲烷-乙醚(2:3)提取后测定,其中色谱柱为Diamonsil C18,流动相为0·05mol·L-1(pH4·8)磷酸二氢钾缓冲液-甲醇-乙腈(61:25:14),流速为1·0mL·min-1,荧光检测器激发波长为334nm,发射波长为385nm。结果:盐酸特拉唑嗪检测浓度在0·25~64ng·mL-1范围内线性关系良好(r=0·9995),最低检测限为0·1ng·mL-1;平均提取回收率为84·0%,平均方法回收率为100·8%;日内RSD≤3·4,日间RSD≤3·0。结论:本方法简便、准确、灵敏,可用于人血浆中盐酸特拉唑嗪的临床药动学研究和血药浓度检测。OBJECTIVE: To establish a RP- HPLC method for the determination of terazosin hydrochloride in human plasma.METHODS:Terazosin hydrochloride and internal standard (parazosin hydrochloride) were extracted from plasma with dichlormethane- diethylether(2 : 3) for determination.The separation was carried on a Diamonsil Cls column with the mobile phase consisted of 0.05mol · L^-1 potassium dihydrogen phosphate buffer solution(pH4.8) -methanol- acetonitrile(61 : 25 : 14) .The flow rate of the mobile phase was 1.0mL · min^-1,and the excitation and emission wavelengths of the florescence detector were set at 334 and 385 nm, respectively.RESULTS:The linear range of terazosin hydrochloride was 0.25-64ng · mL^-1 (r = 0.999 5), with the lowest detectable limit at 0. lng · mL^-1.The average extraction recovery was 84.0% and the average methodological recovery was 100.8% .The intra-day RSD and inter- day RSD were no more than 3.4% and 3.0%, espectively.CONCLUSION:This method is rapid, simple, accurate and sensitive, and suitable for the pharmacokinetic study and assaying of terazosin hydrochloride.
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