Barza M, Kane A, Baum J
Invest Ophthalmol Vis Sci. 1983 Dec;24(12):1602-6.
Although intravitreal injection of antibiotics is being used more widely in treatment of bacterial endophthalmitis, the pharmacokinetic principles that underlie such therapy have been derived exclusively from experiments in the rabbit. Therefore, we studied several representative antibiotics in normal eyes of rhesus monkeys. Carbenicillin (1,000 micrograms), cefazolin (1,000 micrograms), or gentamicin (100 micrograms) was injected intravitreally. Vitreous and aqueous humors were aspirated at intervals up to 96 hours after injection. The half-life values in the vitreous humor were: carbenicillin 10 hours, cefazolin 7 hours, and gentamicin 33 hours. Concomitant intraperitoneal administration of probenecid prolonged the vitreal half-life of carbenicillin to 20 hours and of cefazolin to 30 hours. The estimated vitreous volumes in these monkeys were approximately 3.0-4.0 ml. These results are consistent with the hypothesis that, in primates as in rabbits, beta-lactam antibiotics are eliminated via the retinal route and the aminoglycoside via the anterior route. This supports the applicability of the rabbit model to the treatment of endophthalmitis in humans.
尽管玻璃体内注射抗生素在细菌性眼内炎治疗中的应用越来越广泛,但这种治疗所依据的药代动力学原理完全来自于在兔子身上进行的实验。因此,我们在恒河猴的正常眼睛中研究了几种代表性抗生素。将羧苄青霉素(1000微克)、头孢唑林(1000微克)或庆大霉素(100微克)玻璃体内注射。在注射后长达96小时的间隔时间抽取玻璃体液和房水。玻璃体液中的半衰期值分别为:羧苄青霉素10小时、头孢唑林7小时、庆大霉素33小时。同时腹腔注射丙磺舒可将羧苄青霉素在玻璃体内的半衰期延长至20小时,头孢唑林延长至30小时。这些猴子的估计玻璃体液量约为3.0 - 4.0毫升。这些结果与以下假设一致:在灵长类动物中,如同在兔子中一样,β-内酰胺类抗生素通过视网膜途径消除,氨基糖苷类抗生素通过前部途径消除。这支持了兔子模型在人类眼内炎治疗中的适用性。