Riviere J E, Coppoc G L, Hinsman E J, Carlton W W
Antimicrob Agents Chemother. 1981 Sep;20(3):387-92. doi: 10.1128/AAC.20.3.387.
Most clinical schemes used to adjust gentamicin dosage regimens in renal insufficiency assume that the volume of distribution remains constant. The purpose of this investigation was to determine the pharmacokinetic parameters of gentamicin (two-compartment open model) before and at two points during the acute phase of experimentally induced nephrotoxic (injection of anti-glomerular basement membrane antibody) glomerulonephritis in beagle dogs. Disease was verified by decreased 24-h creatinine clearance, increased 24-h urinary protein excretion, and characteristic immunofluorescent, light- and electron-microscopic lesions. After disease induction, the concentration of drug in serum at time zero (Cp0) was significantly decreased and the volume of the central compartment (Vc) and the volume of distribution (Vd(area)) were increased in all treated dogs. These findings suggest that the assumption of unchanged volume of distribution in acute glomerulonephritis could lead to a serious overestimation of serum drug concentration.
大多数用于调整肾功能不全患者庆大霉素给药方案的临床方案都假定分布容积保持不变。本研究的目的是确定在实验性诱导肾毒性(注射抗肾小球基底膜抗体)的比格犬急性肾小球肾炎急性期之前及期间两个时间点的庆大霉素药代动力学参数(二室开放模型)。通过24小时肌酐清除率降低、24小时尿蛋白排泄增加以及特征性免疫荧光、光镜和电镜病变来证实疾病。诱导疾病后,所有治疗犬的零时血清药物浓度(Cp0)显著降低,中央室容积(Vc)和分布容积(Vd(area))增加。这些发现表明,在急性肾小球肾炎中假定分布容积不变可能导致血清药物浓度的严重高估。