Purpose. To characterize the anterior segment effects of cidofovir, us
ing an animal model. Methods. Cidofovir drops, at concentrations of 0.
04%, 0.4% and 4%, were instilled in eyes of guinea pigs once daily for
10 days. Fellow eyes (controls) received normal saline. The corneal e
pithelium was debrided at day one and then at every other day for 10 d
ays. Subconjunctival injections of 20 mu l of 4% cidofovir were given
in another group of animals. A micromanometer was used to determine th
e intraocular pressure (IOP). Eyes were studied histopathologically at
the conclusion of the study. Results. There was no significant drop i
n IOP after 10 days, using the 0.04% concentration of cidofovir drops.
Histology revealed mild corneal edema and inflammatory infiltrate; ir
is, ciliary body and retina were normal. There was a statistically sig
nificant drop in IOP in the eyes treated with 0.4% and 4.0%, cidofovir
eye drops at 10 days (p = 0.005 and p < 0.0001, respectively) compare
d to baseline. Morphological changes included moderate to severe corne
al edema, vascularization and inflammatory infiltration. The iris and
ciliary body revealed mild inflammatory changes only at the 4% cidofov
ir dose. No changes were seen in the retina with any doses. No change
in IOP was observed following subconjunctival injections of 4% cidofov
ir, and histologically, only localized inflammatory changes in the con
junctiva were observed. Conclusions. The IOP-decreasing effect of cido
fovir occurs at doses below those causing intraocular inflammation and
is likely due to an effect on the anterior segment. The anterior segm
ent effects of cidofovir in guinea pigs were similar to those in human
s. Thus, the guinea pig appears to be a good animal model for studying
the effects of cidofovir on the anterior segment structures.