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作 者:戴青[1] 陈勇川[1] 邱学文[1] 向荣凤[1] 熊丽蓉[1]
机构地区:[1]第三军医大学西南医院药剂科,国家药品临床研究基地,重庆400038
出 处:《药物分析杂志》2013年第9期1486-1490,共5页Chinese Journal of Pharmaceutical Analysis
摘 要:目的:建立测定人体血浆中氨磺必利高效液相色谱法,测定健康志愿者口服氨磺必利片48 h内血药浓度,进行药动学研究。方法:采用10%三氯醋酸直接沉淀提取血浆,固定相为C18,以庚烷磺酸钠醋酸溶液(pH 4.85)-乙腈(80∶20)为流动相,荧光检测波长为λex=280 nm,λem=370 nm。结果:氨磺必利线性范围为5~800 ng·mL-1(r=0.9997),低、中、高3个浓度平均方法回收率分别为105.1%、105.4%、101.3%,日内、日间精密度RSD均<4%;AUC0~∞为(3545.74±1199.58)ng·h·mL-1,AUC0~t为(3348.50±1161.27)ng·h·mL-1,C max为(457.69±232.62)ng·mL-1,T max为(4.15±1.31)h,t1/2为(10.77±5.77)h。结论:本法简便、快速、经济、准确,可用于测定人血浆中氨磺必利的浓度及药动学研究。Objective :To establish an HPLC method for the determination of amisulpride levels in human plasma, determine the amisulpride plasma concentration in healthy volunteers within 48 hours after oral administration of amisulpride tablets, and study on pharmacokineties. Methods:The amisulpride was extracted from plasma by 10% triehloroacetie acid. Chromatographic separation has been achieved on C18 column with sodium heptanesulfonate - acetic acid (pH 4. 85 )and methyl cyanides (80: 20)as the mobile phase. The fluorescence detection was used to de- termine amisulpride atλex = 280 nm and λem = 370 nm. Results:The linear range was 5 - 800 ng . mL-1 (r = 0.9997). The average method recovery of low, middle and high concentration was 105.1%, 105.4%, and 101.3% ,respectively. RSDs of inter - and intra -day precision were both less than 4%. AUC0-∞ was(3545.74 ± 1199.58) ng.h . mL- 1, AUC0-t was ( 3348.50 ± 1161.27 ) ng . h . mL- 1 , Cmax was ( 457.69 ± 232.62 )ng . mL -1, Tmax was (4. 15 ± 1.31 ) h, t1/2 was ( 10. 77 ± 5.77 ) h. Conclusion : The method is simple, rapid, economical and accurate for determination of amisulpride in human plasma and pharmaeokinetie study.
关 键 词:氨磺必利 高效液相色谱法 荧光检测 血药浓度 血浆样品测定 药动学研究
分 类 号:R917[医药卫生—药物分析学]
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