C. Vass et al., Intrascleral concentration vs depth profile of mitomycin-C after episcleral application: Impact of irrigation, EXP EYE RES, 70(2), 2000, pp. 139-143
Mitomycin-C has been reported to cause toxic effects on the ciliary body af
ter episcleral application during glaucoma surgery, We investigated the int
rascleral diffusion of mitomycin-C in an experimental model. The episcleral
sides of scleral quadrants of 14 human donor eyes were exposed for 5 min t
o sponges (corneal light shield, Merocel corp., Mystic, CT, U.S.A.) soaked
with 200 mu g ml(-1) mitomycin-C. After the exposure one of four quadrants
was not irrigated and the episcleral sides of three quadrants were irrigate
d with 40, 100 and 200 ml saline. A 9 mm scleral disk was punched out with
a trephine and frozen on a kryotome plate 2 min after the end of mitomycin-
C exposure. An 8 mm diameter scleral disk was then cut with a trephine, aga
in frozen on a krgotome plate and then horizontally dissected with a kryoto
me. For analysis purposes seven cuts of 20 mu m thickness were combined to
one layer of 140 mu m. Six layers could be reproduced and were analysed. Th
e mitomycin-C concentrations of these layers were analysed by high-performa
nce liquid chromatography. A concentration vs depth profile was calculated
for each group, and the half-width of concentration was calculated by log-l
inear regression.
The mitomycin-C concentration of layer 1 was 24.51 mu g g(-1) (+/-7.52) wit
hout irrigation, 13.15 mu g g(-1) (+/- 4.38) after 40 ml irrigation, 10.29
(+/-3.53) after 100 ml irrigation and 8.4 mu g g(-1) (+/-1.62) after 200 ml
irrigation. In layers 1-3 the concentration of mitomycin-C was significant
ly reduced by irrigation (ANOVA). In the deeper intrascleral layers irrigat
ion had no effect on the mitomycin-C concentrations. Between layers 2 and 6
the half-width of the mitomycin-C concentration was 101 mu m (no-irrigatio
n group), 141 mu m (40 ml irrigation group), 153 mu m (100 ml irrigation gr
oup), and 164 mu m (200 ml irrigation group). Irrigation reduced the mitomy
cin-C concentration only down to half of the scleral thickness, leaving the
deep intrascleral concentrations unchanged. (C) 2000 Academic Press.