C. Bucolo et al., METHYLPREDNISOLONE DELIVERY BY HYALOBEND(R) CORNEAL SHIELDS AND ITS EFFECTS ON RABBIT OCULAR INFLAMMATION, Journal of ocular pharmacology and therapeutics, 12(2), 1996, pp. 141-149
Release of methylprednisolone from hyaluronic acid derivative corneal
shields (Hyalobend(R)), in vitro and in vivo, was evaluated as well as
ocular anti-inflammatory activity in the rabbit eye. The release of m
ethylprednisolone from Hyalobend(R) corneal shields in vitro followed
zero-order kinetics. After placing Hyalobend(R) corneal shields in rab
bit eye, aqueous and tear fluid methylprednisolone levels were detecte
d up to 48 hours and compared with the levels obtained with methylpred
nisolone suspension. Hyalobend(R) corneal shields maintain almost cons
tant methylprednisolone levels in the rabbit tear fluid. On the contra
ry, the suspension gave very high tear values of steroid concentration
s in the first 30 minutes but undetectable in less than 200 minutes. H
yalobend(R) corneal shields ensured effective levels of methylpredniso
lone into the rabbit aqueous for up to 48 hours. Aqueous levels of dru
g, in the group treated with the suspension, decreased progressively a
nd after 480 minutes were undetectable. Hyalobend(R) corneal shields s
ignificantly reduced the conjunctival inflammation elicited by sodium
arachidonate compared with control. Furthermore, Hyalobend(R) corneal
shields treatment significantly reduced the levels of PGE(2) in the te
ar fluid. Hyalobend(R) corneal shields increase the residence time of
methylprednisolone in rabbit tear fluid and enhance the penetration in
to the aqueous humor as well as reduced the primary signs of ocular in
flammation.