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作 者:陈力[1] 唐玲[1] 沈正泽[1] 金梅[1] 向萍[1] 赵国荣[1] 何海霞[2]
机构地区:[1]重庆医科大学附属永川医院,永川区402160 [2]重庆医科大学附属第一医院,重庆市400016
出 处:《中国药房》2010年第41期3875-3877,共3页China Pharmacy
摘 要:目的:研究脂质饮食对莫昔沙星药动学的影响。方法:8只Beagle犬分别在空腹或脂质饮食状态下灌服莫昔沙星胶囊17mg·kg-1,1周后交叉实验;采用高效液相色谱法测定不同时间(72h内)血药浓度,用3p97软件计算二者的药动学参数并进行比较。结果:Beagle犬空腹组和脂质饮食组的药-时曲线分别符合二室模型和一室模型;空腹和脂质饮食状态下莫昔沙星主要药动学参数t1/2(βt1/2ke)分别为(24.89±6.77)、(12.32±2.96)h,tmax分别为(2.00±0.76)、(9.00±1.85)h,Cmax分别为(7.07±0.67)、(4.16±1.32)μg·mL-1,AUC0~t分别为(84.30±10.86)、(85.78±27.38)μg·h·mL-1;除AUC0~t外,其余各参数两两比较均有显著性差异(P<0.01)。结论:脂质饮食可明显延迟莫昔沙星的吸收,不利于其抗菌作用的发挥。OBJECTIVE:To study the effect of lipide diet on pharmacokinetics of moxifloxacin.METHODS:In randomized crossover experiment,8 Beagle dogs were given moxifloxacin 17 mg·kg^-1 at the condition of empty stomach or after lipide diet for 1 week.Plasma concentration of moxifloxacin was determined by HPLC at different time(during 72 h).The pharmacokinetic parameters were calculated by 3p97 software.RESULTS:The plasma concentration-time curves were two or one compartment model at the condition of empty stomach or after lipide diet.Main pharmacokinetic parameters were as follows:t1/2β(t1/2ke):(24.89±6.77) h vs.(12.32±2.96) h;tmax:(2.00±0.76) h vs.(9.00±1.85) h;Cmax:(7.0±0.67) μg·mL^-1 vs.(4.16±1.32) μg·mL^-1;AUC0~t:(84.30±10.86) μg·h·mL^-1 vs.(85.78±27.38) μg·h·mL^-1,respectively.There were significant differences in pharmacokinetic parameters except for AUC0~t(P0.01).CONCLUSION:Lipide diet can delay the absorption of moxifloxacin and inhibit its antibacterial activity.
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