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Vol. 30, Issue 4, 421-429, April 2002
Allergan, Inc., Irvine, California (A.A.A., M.S., J.B., L.W.,
D.T.-L.); and Huntingdon Life Sciences, Huntingdon, Cambridgeshire,
United Kingdom (B.J.)
The objectives of the study were to evaluate the distribution of
brimonidine (
2-adrenergic agonist) into anterior and
posterior ocular tissues. Single or multiple doses of a 0.2 or 0.5%
brimonidine tartrate solution were administered to one or both eyes of
monkeys or to one eye of rabbits. Brimonidine was administered
intraperitoneally to rats. After topical administration,
[14C]brimonidine was rapidly absorbed into the cornea and
conjunctiva and distributed throughout the eye.
[14C]Radioactivity was higher and cleared more slowly in
pigmented tissues (iris/ciliary body, choroid/retina, and optic nerve)
than in nonpigmented tissues. Single and multiple dosing led to a
similar drug distribution, with higher levels of brimonidine measured in pigmented tissues after multiple dosing. Most of the radioactivity extracted from ocular tissues represented unchanged brimonidine. In the
rabbits and the monkey treated in only one eye, levels of radioactivity
in the untreated eye were low, consistent with the low systemic levels
and rapid drug clearance. Posterior ocular tissue concentrations of
radioactivity exceeded systemic blood concentrations. The vitreous
humor brimonidine concentrations in monkeys treated topically with
0.2% brimonidine tartrate was 82 ± 45 nM. Vitreous levels in
rabbits confirmed the penetration of brimonidine to the posterior
segment. Similar concentrations of brimonidine (22 to 390 nM) were
measured in the vitreous and retina of rats injected intraperitoneally
with brimonidine. Both topically applied and systemically administered
brimonidine reach the back of the eye at nanomolar concentrations
sufficient to activate
2-adrenergic receptors. The
brimonidine levels achieved at the retina are relevant for
neuroprotection models.
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