Cheymol G, Bernheim C, Besson J, Dry J, Portet R
Br J Clin Pharmacol. 1979 Mar;7(3):303-9. doi: 10.1111/j.1365-2125.1979.tb00937.x.
1 Thirty-three patients with no evidence of endocrine disease, hepatic or renal insufficiency or sleep disorders, were classified in groups 1 to 4 in order of increasing of percentage of ideal body weight (IBW) respectively: less than 90% of IBW, 90--120%, 120--180%, and greater than 180% of IBW. After oral administration of 200 mg butobarbitone, concentration of the intact drug was measured by gas liquid chromatographic assay in urine samples collected during 72 h and at three times in blood. 2 A highly significant negative relationship was found between the cumulative excretion of butobarbitone with urine and the logarithm of the percentage of IBW. In contrast for a given weight, excretion of the drug with urine was found to be weakly correlated with the diuresis. 3 The cumulative urinary elimination of butobarbitone was significantly different between the groups studied, except of the difference between the group 2 and 3 of the patients. No significant difference was found between the renal clearances of butobarbitone in the four groups of subjects. 4 We conclude that redistribution of butobarbitone into adipose tissues can explain the obtained results and that obesity modifies the pharmacokinetics of the drug.
33名无内分泌疾病、肝肾功能不全或睡眠障碍证据的患者,根据理想体重(IBW)百分比的增加顺序分别分为1至4组:低于IBW的90%、90%-120%、120%-180%以及高于IBW的180%。口服200毫克布他比妥后,通过气液色谱分析法测定在72小时内收集的尿液样本以及在三个时间点采集的血液样本中完整药物的浓度。
发现布他比妥随尿液的累积排泄量与IBW百分比的对数之间存在高度显著的负相关关系。相比之下,对于给定体重,药物随尿液的排泄量与尿量之间的相关性较弱。
除了第2组和第3组患者之间的差异外,所研究组之间布他比妥的累积尿排泄量存在显著差异。四组受试者中布他比妥的肾清除率之间未发现显著差异。
我们得出结论,布他比妥在脂肪组织中的再分布可以解释所获得的结果,并且肥胖会改变该药物的药代动力学。