Kitaura T, Tsukiai S, Arai S, Miyake K, Kimura M, Fukuchi H
Department of Pharmaceutical Services, Hiroshima University Hospital, Japan.
J Pharmacobiodyn. 1988 Oct;11(10):694-9. doi: 10.1248/bpb1978.11.694.
Penetrations of latamoxef (LMOX) and cefaclor (CCL) into the aqueous humor after intravenous or oral administration were investigated in rabbits. Concentrations of antibiotics in plasma and aqueous humor after administration were determined periodically by microbiological assay. LMOX disappeared from plasma in a monoexponential manner with a half-life of 43 min after intravenous administration at a dose of 50 mg/kg. The maximum concentration of LMOX in aqueous humor (6.4 micrograms/ml) was observed 1 h after administration. When CCL was administered orally at a dose of 50 mg/kg, the maximum concentration of CCL in aqueous humor was 1.00 microgram/ml 1.5 h after administration, whereas the maximum plasma concentration of 19.2 micrograms/ml was observed at 30 min. Pharmacokinetic analysis (simultaneous simulation) of plasma and aqueous humor concentration-time courses was made using the best fitted compartment model examined (modified two-compartment model). Prediction of the concentration of antibiotics in aqueous humor from the plasma concentration profile was also examined using the same compartment model in a separate experiment. The predicted concentration in aqueous humor was proved to coincide reasonably well with the measured concentration.
在兔子身上研究了静脉注射或口服拉氧头孢(LMOX)和头孢克洛(CCL)后抗生素在房水中的渗透情况。给药后定期通过微生物学测定法测定血浆和房水中抗生素的浓度。静脉注射剂量为50mg/kg的LMOX后,其在血浆中呈单指数方式消失,半衰期为43分钟。给药后1小时观察到房水中LMOX的最大浓度为6.4微克/毫升。当口服剂量为50mg/kg的CCL时,给药后1.5小时房水中CCL的最大浓度为1.00微克/毫升,而在30分钟时观察到血浆最大浓度为19.2微克/毫升。使用所检验的最佳拟合房室模型(改良二室模型)对血浆和房水浓度-时间过程进行药代动力学分析(同步模拟)。在另一个实验中,还使用相同的房室模型检验了根据血浆浓度曲线预测房水中抗生素浓度的情况。结果证明,房水中预测浓度与实测浓度相当吻合。