Ellis P P, Rendi M A
Can J Ophthalmol. 1981 Apr;16(2):79-83.
A study was undertaken to determine the extent of inactivation of gentamicin, tobramycin, ticarcillin and carbenicillin when given subconjunctivally in amino-glycoside-penicillin combinations. Rabbits were injected with such a combination in either the same or opposite subconjunctival sites. The aqueous humor was aspirated and bioassayed for antibiotic activity at 1 and 4 hours after injection. The influence of the aqueous humour upon antibiotic inactivation was studied by in vitro experiments. Ticarcillin penetrated into the aqueous humour better than carbenicillin. Some chemical inactivation of all the antibiotics given in combination occurred. There was less inactivation of the aminoglycosides at 4 hours when the antibiotics had been injected at opposite poles. The inactivation occurred primarily within the aqueous humour but to a lesser extent in the subconjunctival space. The degree of inactivation is likely of little clinical significance with the doses usually used.
进行了一项研究,以确定庆大霉素、妥布霉素、替卡西林和羧苄西林以氨基糖苷类 - 青霉素组合结膜下给药时的失活程度。将这些组合注射到兔子的同侧或对侧结膜下部位。在注射后1小时和4小时抽取房水并进行抗生素活性生物测定。通过体外实验研究了房水对抗生素失活的影响。替卡西林比羧苄西林更易渗透到房水中。联合使用的所有抗生素都发生了一些化学失活。当抗生素在对侧极点注射时,4小时时氨基糖苷类的失活较少。失活主要发生在房水中,但在结膜下间隙中程度较小。就通常使用的剂量而言,失活程度可能没有什么临床意义。