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作 者:屠文莲[1] 赵银[1] 王宇[1] 夏爱博[1] 赵刚[1]
出 处:《中国新药与临床杂志》2013年第6期486-489,共4页Chinese Journal of New Drugs and Clinical Remedies
基 金:云南省自然科学基金资助项目(2000C0106M)
摘 要:目的建立高效液相色谱(HPLC)法测定小鼠血清中痂囊腔菌素A的浓度,考察其在小鼠体内的药动学特征。方法60只小鼠,雌雄各半,痂囊腔菌素A30.0mg灌胃后,于不同时间点分取血浆,采用HPLC分别测定血清样品中痂囊腔菌素A浓度,用DAS3.0.8软件计算药动学参数。结果痂囊腔菌素A在10.0~800.0μg·L-1内线性关系良好(r=0.9996),日内和日间RSD〈7.0%,提取回收率为89-2%~92.4%,方法回收率为100.1%~100.6%。痂囊腔菌素A在小鼠体内的主要药动学参数:AUC。匀(16697.8-4-873.0)μg-L·h-1,MRTo。为(3.8±0.0)h,:为(3.6±0.0)h,为(1.0±0.0)h,CLz/F为(1.8±0.0)L-h,p-1为(5889.3±135.9)μg·L-1。结论本法简便、灵敏、重现性好。痂囊腔菌素A在小鼠体内药动学过程符合二室模型。AIM To establish a HPLC method for determining the serum concentration of elsinochrome A and to investigate its pharmacokinetic in mice. METHODS After the plasma from 60 mice (half male and half female) with intragastric were collected in different time point, elsinochrome A in serums were collected and determined by HPLC. The pharmacokinetic parameters were calculated by DAS 3.0.8. RESULTS The good linear range of elsinochrome A were from 10.0 - 800.0 gL-1(r = 0.999 6). The limit of quantitation (LOQ) was 1.0 g.L-1. The RSD (%) of intra-and inter-day were all below 〈 7.0%. The extraction recoveries were in the range of 89.2% - 92.4% and the method recoveries were 100.1% - 100.6%. The main pharmacokinetic parameters of mice were as follows: AUC0 (16 697.8 ±873.0) μg.Lh-1, MRT0 = (3.8 ± 0.0) h,z = (3.6 ± 0.0) h, t,r = (1.0 ±0.0) h, CLz/F= (1.8 ± 0.0) L.h-1, p = (5 889.3 ± 135.9) μg.L-1. CONCLUSION This method is convenient, sensitive and reproducible. The pharmacokinetic character of Elsinochrome A in mouse after oral showes linear and conforms to the two compartment models.
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