McDermott M L, Hazlett L D, Barrett R
Department of Opthalmology, Kresge Eye Institute, Wayne State University, Detroit, Michigan 48201, USA.
Cornea. 1997 Mar;16(2):209-14.
Possible toxic effects of ofloxacin on human corneal endothelia were assessed by using electron microscopy and in vitro specular perfusion.
Five pairs of corneas [with one cornea of each pair receiving balanced salt solution (Endosol; Allergan, Irvine, CA, U.S.A.) and the other receiving Endosol with 10 micrograms/ml of ofloxacin] underwent perfusion for 3 h with corneal pachymetry every 15 min followed by tissue fixation. A mean corneal swelling rate was calculated from a first-order regression line fit for each of the five experiments. The swelling rates between groups was compared by-using a paired t test. Scanning and transmission electron micrographs were examined for cellular architecture. Another group of five pairs of corneas was perfused the same way with the only difference being a test dose of 30 micrograms/ml.
The mean swelling rate for corneas perfused with 10 micrograms/ml of ofloxacin of -3.5 microns/h was not significantly different from that of the Endosol-alone corneas at -3.0 microns/h (p = 0.71). The mean swelling rate for corneas perfused at 30 micrograms/ml of ofloxacin was -4.1 microns/h, not significantly different from Endosol-alone perfused corneas at -6.5 microns/h (p = 0.08). No consistent ultrastructural changes could be attributed to exposure to 10 or 30 micrograms/ml of ofloxacin.
Human corneal endothelium can be exposed to ofloxacin at a dose of 30 micrograms/ml for a period of 3 h without adverse ultrastructural or physiologic side effects.
通过电子显微镜检查和体外镜面灌注评估氧氟沙星对人角膜内皮细胞的潜在毒性作用。
五对角膜[每对中的一个角膜接受平衡盐溶液(Endosol;美国加利福尼亚州欧文市的Allergan公司),另一个接受含10微克/毫升氧氟沙星的Endosol]进行3小时的灌注,每15分钟测量一次角膜厚度,随后进行组织固定。根据五个实验中每个实验的一阶回归线拟合计算平均角膜肿胀率。使用配对t检验比较各组之间的肿胀率。检查扫描和透射电子显微镜照片以观察细胞结构。另一组五对角膜以相同方式进行灌注,唯一的区别是测试剂量为30微克/毫升。
用10微克/毫升氧氟沙星灌注的角膜平均肿胀率为-3.5微米/小时,与仅用Endosol灌注的角膜(-3.0微米/小时)相比无显著差异(p = 0.71)。用30微克/毫升氧氟沙星灌注的角膜平均肿胀率为-4.1微米/小时,与仅用Endosol灌注的角膜(-6.5微米/小时)相比无显著差异(p = 0.08)。未发现一致的超微结构变化可归因于暴露于10或30微克/毫升的氧氟沙星。
人角膜内皮细胞可以暴露于30微克/毫升的氧氟沙星中3小时,而不会产生不良的超微结构或生理副作用。