Bruguerolle B, Prat M
J Pharm Pharmacol. 1987 Feb;39(2):148-9. doi: 10.1111/j.2042-7158.1987.tb06966.x.
The chronokinetics of bupivacaine have been examined in the mouse. Different groups of adult male NMRI mice maintained under controlled environmental conditions received a single intraperitoneal injection of bupivacaine (20 mg kg-1) at one of four different fixed time points in a 24 h period i.e. 10:00, 16:00, 22:00 and 04:00 h. Blood samples were taken 0.25, 0.5, 0.75, 1, 1.5, 3, 4 and 6 h after drug administration and total serum levels of bupivacaine were determined by a gas-liquid chromatography with a flame ionization detector. Statistically significant temporal changes were found in the following pharmacokinetic parameters: highest Cmax value = 0.900 +/- 0.080 micrograms mL-1 at 22:00 h (amplitude, maximum-minimum/mean X 100, is 64%); highest Cmax/Tmax ratio = 3.596 +/- 0.339 at 22:00 h (amplitude = 85%); highest beta elimination half-life, T1/2 beta, = 3.950 +/- 0.246 h at 22:00 h (amplitude = 35%); area under concentration curve (AUC infinity 0) was not found to be significantly different among the hours of administration. The temporal kinetic changes demonstrated suggest a possible circadian difference in bupivacaine efficacy and/or toxicity.
已在小鼠中研究了布比卡因的时效动力学。将成年雄性NMRI小鼠分成不同组,在可控环境条件下饲养,于24小时内四个不同的固定时间点之一,即10:00、16:00、22:00和04:00,单次腹腔注射布比卡因(20 mg kg-1)。给药后0.25、0.5、0.75、1、1.5、3、4和6小时采集血样,采用带火焰离子化检测器的气液色谱法测定布比卡因的总血清水平。在以下药代动力学参数中发现了具有统计学意义的时间变化:最高Cmax值 = 0.900 +/- 0.080微克/毫升,出现在22:00时(波动幅度,最大值 - 最小值/平均值×100,为64%);最高Cmax/Tmax比值 = 3.596 +/- 0.339,出现在22:00时(波动幅度 = 85%);最高β消除半衰期,T1/2β, = 3.950 +/- 0.246小时,出现在22:00时(波动幅度 = 35%);给药各小时之间的浓度曲线下面积(AUC infinity 0)未发现有显著差异。所显示的时效动力学变化表明布比卡因的疗效和/或毒性可能存在昼夜差异。