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    冰片对吉西他滨在脑胶质瘤模型大鼠体内药动学的影响

    Effects of borneol on the pharmacokinetics of gemcitabine in 9Lacz cell-bearing rats

    • 摘要: 目的 考察冰片对吉西他滨在9Lacz脑胶质瘤模型大鼠体内药动学的影响。方法 建立大鼠9Lacz脑胶质瘤动物模型。模型大鼠随机分为3组,分别为单用吉西他滨给药组(吉西他滨150 mg/kg)、溶媒对照组(吉西他滨150 mg/kg+溶媒2 ml)、吉西他滨联合冰片给药组(吉西他滨150 mg/kg+300 mg/kg冰片混悬溶液)。利用微透析法于注射后系列时间点收集脑肿瘤侧透析液,采用UPLC-MS/MS法检测透析液中吉西他滨的浓度,并计算其药动学参数。结果 吉西他滨联合冰片给药组与单用吉西他滨组比较,Cmax及AUC(0-∞)增加,t1/2延长,差异有统计学意义(P<0.01)。结论 冰片可提高吉西他滨在9Lacz脑胶质瘤模型大鼠脑肿瘤区域的生物利用度。

       

      Abstract: Objective To investigate the effects of borneol on the pharmacokinetics of gemcitabine in 9Lacz cell-bearing rats. Methods A rat model of glioma was established using 9Lacz cells. The modeled rats were randomly divided into three groups: a gemcitabine group (150 mg/kg gemcitabine), a vehicle control group (150 mg/kg gemcitabine+2 ml vehicle), and a gemcitabine combined with borneol group (150 mg/kg gemcitabine+300 mg/kg borneol). Then,the microdialysis sampling method was used to collect microdialysis solution around the brain tumor at different time points, where the concentration of gemcitabine was detected by UPLC-MS/MS. The pharmacokinetic parameters were calculated. Results The gemcitabine and borneol group presented remarkable increases in the values of t1/2、AUC(0-∞) and Cmax, compared with the gemcitabine group (P<0.01). Conclusions Borneol can improve the bioavailability of gemcitabine in 9Lacz cell-bearing rats.

       

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