Schwartz S N, Pazin G J, Lyon J A, Ho M, Pasculle A W
J Infect Dis. 1978 Oct;138(4):499-505. doi: 10.1093/infdis/138.4.499.
For determination of the best basis on which to calculate dosages of gentamicin or tobramycin to be administered to obese patients, the pharmacokinetics of these drugs were studied in 13 obese subjects and 13 subjects of a normal weight following intravenous infusion of 1 mg/kg. Half-lives, elimination constants, and absolute and relative volumes of distribution were calculated. Concentrations of drug in serum were significantly higher and relative volumes of distribution were significantly lower in obese subjects as compared with controls. However, relative volumes of distribution based on lean body mass of obese subjects were significantly greater than those of normal-weight subjects. These results indicate that gentamicin and tobramycin are distributed less to adipose tissue than to other tissues, but partial distribution to adipose tissue does occur. The mean relative volume of distribution in obese subjects closely approximated that in normal subjects when normalized body mass plus 40% of the adipose mass was used as the total weight in obese subjects.
为确定计算肥胖患者庆大霉素或妥布霉素给药剂量的最佳依据,对13名肥胖受试者和13名正常体重受试者静脉输注1mg/kg后这两种药物的药代动力学进行了研究。计算了半衰期、消除常数以及绝对和相对分布容积。与对照组相比,肥胖受试者血清中的药物浓度显著更高,相对分布容积显著更低。然而,基于肥胖受试者瘦体重的相对分布容积显著大于正常体重受试者。这些结果表明,庆大霉素和妥布霉素在脂肪组织中的分布少于其他组织,但确实会部分分布到脂肪组织中。当将肥胖受试者的体重标准化后加上40%的脂肪量作为总体重时,肥胖受试者的平均相对分布容积与正常受试者的非常接近。