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作 者:陈亚军[1] 王淑君[1] 汪珊珊[1] 汪电雷[1,2] 何黎琴[1] 李君耀 严丹丹[1] 王雪琦[1] 李洁[1] 彭兆亮[1]
机构地区:[1]安徽中医药大学药学院 [2]安徽中医药大学药物代谢动力学研究室
出 处:《中国临床药理学与治疗学》2015年第4期374-378,共5页Chinese Journal of Clinical Pharmacology and Therapeutics
基 金:国家自然科学基金资助项目(81473536;81001592);国家重大新药创制资助项目(2009ZX09103-399);安徽科技厅科技攻关项目(1301042097)
摘 要:目的:建立测定大鼠血浆中藤黄酸葡萄糖酯浓度的UPLC方法,并探讨其在大鼠体内的药代动力学。方法: 以新藤黄酸为内标,建立大鼠血浆中藤黄酸葡萄糖酯的UPLC测定方法。采用该方法测定大鼠单剂量静脉注射2、4 、8 mg/kg 藤黄酸葡萄糖酯后,不同时间点大鼠血浆中的藤黄酸葡萄糖酯的浓度,对其血药浓度时间采用DAS2.1 软件拟合,计算药动学参数。结果: 血浆中藤黄酸葡萄糖酯在0.05~14.0 mg/L 浓度范围内线性关系良好(r=0.9999) ,定量下限为0.05 mg/L,提取回收率均大于87%,其日内日间RSD均小于10% ,藤黄酸葡萄糖酯按2、4和8 mg/kg 静脉给药后,在大鼠体内的t1/2分别为(16.66±1.56)、(16.81±2.21) 和(17.88±2.05) min,AUC0-t 分别为(12.92±13.14)、(37.3±18.58) 和 (68.22±20.91) min?mg?L-1。结论:所建立的UPLC方法操作简便、快速、专属性强,能满足藤黄酸葡萄糖酯在大鼠体内的药代动力学研究。AIM: To develop an UPLC method for the determination of plasma concentration of gly- co-gambogic acid (Glyco-GA) and study the phar- macokinetics of Glyco-GA in rat plasma. METH- ODS: An UPLC method was established for the de- termination of Glyco-GA in rat plasma and using Gambogenic acid as the internal standard. The plas- ma concentration of Glyco-GA in rats was deter- mined by UPLC after intravenous administration of Glyco-GA at a does of 2, 4 and 8 mg/kg, and the pharmacokinetic parameters were calculated by DAS 2.1. RESULTS:Calibration curve was linear over the range of 0.05 - 14.0 mg/L ( r = 0. 9999 ). The lower limit of quantification was 0.05 mg/L. The extraction recoveries were higher than 87%. The in- tra-day and inter-day precision (RSD%) was lower than 10%, respectively. This method was applied to a pharmacokinetic study after i.v. administration of Glyco-GA in rats at a does of 2, 4 and 8 mg/kg. The T1/2 of Glyco-GA was ( 16.66 ± 1.56), ( 16.81 ±2.21) and (17.88 ±2.05) rain, the AUG_0-t was (12.92 ±13.14), (37.3 ±18.58) and (68.22 ± 20.91 ) min · mg · L^-1, respectively. CONCLU- SION: A simple, rapid and specific UPLC method for the analysis of Glyco-GA was successfully devel- oped and applied to a pharmacokinetic study of Gly- co-GA in rat plasma.
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