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兔血浆利福平的反相高效液相色谱分析及药代动力学研究
引用本文:马荣,陈振,张惠勇,刘晓印,杨小英,党宏万,戈朝晖.兔血浆利福平的反相高效液相色谱分析及药代动力学研究[J].宁夏医科大学学报,2014(1):25-28.
作者姓名:马荣  陈振  张惠勇  刘晓印  杨小英  党宏万  戈朝晖
作者单位:[1]宁夏医科大学,银川750004 [2]宁夏医科大学总医院药剂科,银川750004 [3]宁夏医科大学总医院骨科,银川750004
基金项目:国家自然科学基金(30960391); 宁夏自然科学基金(NZ13144)
摘    要:目的建立兔血浆利福平(rifampicin,RFP)反相高效液相色谱分析方法(reversed-phase high-performance liquid chromatography,RP-HPLC)。研究其静脉给药后兔体内血浆药代动力学参数。方法以Agilent ZORBAX XDB-C18柱(5μm,4.6mm×150mm)为分析柱,流动相为0.02mol·L^-1磷酸二氢钠缓冲液(PH7.0)∶甲醇=30∶70;流速1.0mL·min^-1;柱温:35℃,检测波长330nm。8只新西兰大白兔分别按RFP12mg·kg^-1静滴,RP-HPLC法检测血浆药物浓度。所得血药浓度数据经DAS软件拟合分析。结果 RFP在0.5~72μg·mL^-1血浆浓度范围内线性关系良好(r=0.99969),平均提取回收率为99.72%,日内、日间变异系数(RSD=5)分别为2.6%~4.4%和2.2%~2.9%。静脉滴注RFP在兔体内药代动力学过程符合双隔室模型(权重系数为1/cc),T1/2=(2.87±0.78)h,Cmax=(12.49±1.57)mg·L^-1,AUC(0-∞)=(50.05±14.50)mg·(h·L)^-1。结论本研究建立的兔血浆利福平RP-HPLC方法简便、准确、重现性好,可用于兔体内利福平血药浓度的测定,兔体内利福平药代动力学过程符合双隔室模型,体内药代谢动力学参数为利福平其它剂型的研究提供参考。

关 键 词:利福平  血浆  高效液相色谱法  药代动力学

RP-HPLC Determination and Pharmacokinetic Study of Rifampicin in Rabbit Plasma
MA Rong,CHEN Zhen,ZHANG Huiyong,LIU Xiaoyin,YANG Xiaoying,DANG Hongwan,GE Zhaohui.RP-HPLC Determination and Pharmacokinetic Study of Rifampicin in Rabbit Plasma[J].Journal of Ningxia Medical College,2014(1):25-28.
Authors:MA Rong  CHEN Zhen  ZHANG Huiyong  LIU Xiaoyin  YANG Xiaoying  DANG Hongwan  GE Zhaohui
Institution:1. Graduate School of Ningxia Med. Univ. , Yinehuan 750004 ; 2. Dept. of Pharmacy, General Hospital of Ningxia Med. Univ. , Yinchuan 750004; 3. Dept . of Orthopedics Sugery, the General Hospital of Ningxia Med. Univ. , Yinchuan 750004)
Abstract:Objectiye To develop a method for determination of rifampicin (RFP) in plasma samples by reversed -phase high- performance liquid chromatography( RP- HPLC) and to explore the pharmacokinetic of RFP in rabbits. Methods RP - HPLC was carried out on a Agilent ZORBAX XDB - C18 column(5μm,4.6mm×150mm) using 0.02mol· L^-1 phosphate buffer methanol (30: 70, adjusted pH to 7.0) at 1.0 mL · min^-1. The plasma were analyzed at 330 nm wavelength after methanol protein precipitation. 8 New Zealand white rabbits were injected intravenously by 12mg · kg^-1 INH . Plasma concentration data obtained were fitted by DAS software. Results There was a good linear relationship within the range of 0.5 - 72μg · mL^-1 ( r = 0. 99969). The extraction recovery was 99.72%. The precsion of intro - day and inter - day was 2.6% 4.4% and 2.2% -2.9% ,respectively. RFP pharmacokinetics in rabbits process was in line with double compartment model( weighting factor for the 1/cc), T1/2 = (2.87 ± 0. 78 ) h, Cmax = ( 12.49± 1.57 ) mg · L^-1, AUC(0-∞) = (50.05 ± 14.50) mg·(h · L)^-1. Conclusion This method is simple, accurate, reproducible, and suitable for the determination of pharmacokinetics rifampicin in rabbit plasma. RFP pharmacokinetics in rabbits process in line with double compartment model , In vivo drug of pharmacokinetics provide the reference to the research of rifampicin other dosage forms.
Keywords:rifampicin  plasma  HPLC  pharmacokinetic
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