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大鼠离体原代肝细胞中布洛芬代谢的研究
引用本文:张文军,姜红,娄建石,焦建杰,董伟林,朱立勤.大鼠离体原代肝细胞中布洛芬代谢的研究[J].中国药房,2008,19(7):508-510.
作者姓名:张文军  姜红  娄建石  焦建杰  董伟林  朱立勤
作者单位:1. 天津医科大学总医院药剂科,天津市,300052
2. 天津医科大学总医院药剂科,天津市,300052;天津医科大学药理学教研室,天津市,300070
3. 天津医科大学药理学教研室,天津市,300070
4. 天津医科大学实验中心,天津市,300070
5. 天津市第一中心医院,天津市,300192
摘    要:目的:研究布洛芬在大鼠原代培养肝细胞中的代谢情况。方法:建立大鼠肝细胞的分离及原代培养方法,考察肝细胞对布洛芬的代谢情况;采用2步灌流技术并运用胶原酶消化法,分离肝细胞并分别与2.50、5.00、20.00μg·mL-1浓度布洛芬进行悬浮共培养,在不同时间点取样,应用高效液相色谱法测定布洛芬的浓度并计算其它药动学参数。结果:240min内肝细胞活率>80%,能满足代谢要求;布洛芬低、中、高3种浓度药动学数据Ke为(0.0064±0.0011)、(0.0086±0.009)、(0.0091±0.0015)min-1,t1/2为(110.0562±17.16)、(81.3873±9.2815)、(77.9516±12.1355)min;AUC为(272.9287±35.58)、(448.9899±23.0295)、(2157.6777±318.8730)μg·mL·min-1;CLs为(0.0093±0.0011)、(0.0112±0.0005)、(0.0094±0.0014)mL·min-1。结论:利用原代肝细胞培养技术对布洛芬代谢进行研究,可为临床优化治疗、合理用药等方面提供有价值的实验数据。

关 键 词:布洛芬  大鼠  肝细胞  代谢  药动学参数
文章编号:1001-0408(2008)07-0508-03
收稿时间:2007-04-05
修稿时间:2007-05-29

Metabolism of Ibuprofen in Primarily Cultured Hepatocytes of Rats
ZHANG Wen-jun,JIANG Hong,LOU Jian-shi,JIAO Jian-jie,DONG Wei-lin,ZHU Li-qin.Metabolism of Ibuprofen in Primarily Cultured Hepatocytes of Rats[J].China Pharmacy,2008,19(7):508-510.
Authors:ZHANG Wen-jun  JIANG Hong  LOU Jian-shi  JIAO Jian-jie  DONG Wei-lin  ZHU Li-qin
Institution:ZHANG Wen-jun, JIANG Hong, JIANG Hong, LOU Jian-shi, JIAO Jian-jie, DONG Wei-lin, ZHU Li-qin(1. Dept. of Pharmacy, The General Hospital of Tianjin Medical University, Tianjin 300052, China;2. Dept. of Pharmacology, Tianjin Medical University, Tianjin 300070, China;3. Laboratory Center, Tianjin Medical University, Tianjin 300070, China;4. Tianjin First Central Hospital, Tianjin 300192, China)
Abstract:OBJECTIVE: To study the metabolism of ibuprofen in primarily cultured hepatocytes of rats. METHODS: The method for the isolation and primary culture of rats' hepatocytes was establisehed and the metabolism of ibuprofen in isolated hepatocytes was investigated. Hepatocytes were isolated from rats using two step perfusion and collagenase digestion procedure and co-cultured with different concentrations of ibuprofen (2.50, 5.00, and 20.00 μg·mL^-1, respectively) . Samples were taken at different time point for the HPLC determination of concentration of ibuprofen in hepatocyte suspension and computation of its pharmacokinetic parameters. RESULTS: The metabolism of ibuprofen could be achieved if hepatocytes activity was more than 80% in 240 min. The pharmacokinetic parameters of ibuprofen at low, middle and high concentrations were as follows: Ke: (0.006±0.0011), (0.0086±0.009), and (0.0091±0.0015) min^-1, respectively; t1/2(110.0562±17.16), (81.3873±9.2815), and (77.9516±12.1355) min, respectively; AUC: (272.9287±35.58), (448.9899±23.0295), and (2 157.6777±318.8730)μg·mL·min^-1, respectively. CLs: (0.0093±0.0011), (0.0112±0.0005), and (0.0094±0.0014) mL·min^-1 respectively. CONCLUSION: Applying primary hepatocyte culture technology in the study of metabolism of ibuprofen cau provide valuable experiment data for clinical optimal treatment and rational use of drugs etc.
Keywords:Ibuprofen  Rats  Hepatocyte  Metabolism  Pharmacokinetic parameters
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