Institutional members access full text with Ovid®

Share this article on:

The Efficacy of Topical Ciprofloxacin and Norfloxacin in the Treatment of Experimental Pseudomonas Keratitis.

Reidy, James J. M.D.; Hobden, Jeffery A. M.S.; Hill, James M. Ph.D.; Forman, Kim; O'Callaghan, Richard J. Ph.D.
Cornea: January 1991

: An aminoglycoside-resistant strain of Pseudomonas aeruginosa was injected intrastromally into the corneas of rabbits, and keratitis was allowed to develop over a 22-h period. Rabbits were treated with either 0.75% ciprofloxacin, 1% norfloxacin, or 1.36% tobramycin administered topically every 15 min for 1 h and then every 30 min for the following 3 h. All therapy ceased 26 h postinoculation. Rabbits were killed 1 h after the treatment, and the number of bacteria per cornea were quantified in terms of bacterial colony-forming units. Aqueous humor specimens were obtained from rabbits receiving norfloxacin and ciprofloxacin, and bioassays were performed to determine drug concentration. Ciprofloxacin caused a 5 log reduction in the number of bacterial colony-forming units, as compared with untreated controls (p < 0.0001); it also produced a significantly greater reduction in bacterial colony-forming units than either norfloxacin or fortified tobramycin drops (p < 0.0001). Norfloxacin produced a 2 log reduction in bacterial colony-forming units, as compared with untreated controls (p < 0.0001). The mean aqueous concentration of norfloxacin (7.5 [mu]g/ml) was substantially less than that achieved by ciprofloxacin (30.5 [mu]g/ml). We conclude that ciprofloxacin may be a useful broad spectrum, topical chemotherapeutic agent in the therapy of aminoglycoside-resistant P. aeruginosa keratitis.

(C) Lippincott-Raven Publishers.