We reviewed the results of sterility testing from culture media of 1,1
34 donor corneas preserved by organ culture at 37-degrees-C in our eye
bank. All corneas were stored in minimal essential medium containing
2% fetal calf serum, 0.1 mg/ml penicillin G, 0.1 mg/ml streptomycin, a
nd 2.5 mug/ml amphotericin B. After removal of ocular adnexal tissue,
donor globes were rinsed with sterile saline solution, incubated in 3%
polyvinylpyrrolidone-iodine solution for 3-5 min, and subsequently ri
nsed again with sterile saline solution. Samples for microbiological e
valuation were obtained from the initial evaluation medium, at every m
edium change (every 10 days), and from the medium used for deswelling
of the individual cornea 1 day before transplantation. Incidence of co
ntamination was 0.53% (6 of 1,134 corneas). Three corneas were contami
nated by Micrococcus species, three by fungi. We conclude from our stu
dy that a combination of rinsing donor globes with sterile saline solu
tion, the initial use of a disinfectant, and the employment of penicil
lin/streptomycin and amphotericin B in the organ culture medium, which
have been commonly used in cell culture for decades, result in a low
incidence of bacterial and fungal contamination of corneas preserved b
y organ culture.