1. Vitreous concentration of topically applied brimonidine-purite 0.15%.
- Author
-
Kent AR, King L, and Bartholomew LR
- Subjects
- Administration, Topical, Adrenergic alpha-Agonists pharmacokinetics, Aged, Biological Availability, Brimonidine Tartrate, Female, Gas Chromatography-Mass Spectrometry, Humans, Male, Ophthalmic Solutions pharmacokinetics, Tissue Distribution, Vitrectomy, Antihypertensive Agents pharmacokinetics, Quinoxalines pharmacokinetics, Vitreous Body metabolism
- Abstract
Purpose: The aim of this study was to determine the vitreous brimonidine concentration of topically applied brimonidine-Purite 0.15%., Methods: Patients scheduled for a pars plana vitrectomy were invited to participate in this study after institutional review board (IRB) approval was obtained. Each patient was asked to apply brimonidine-Purite (0.15%) drops in the designated eye either every 12 h (b.i.d.; 9 patients) or every 8 h (t.i.d.; 10 patients) for the 2 weeks proceeding scheduled surgery. The importance of the last topical dose being 12 h (b.i.d. group) or 8 h (t.i.d. group) before the scheduled surgery, was emphasized. Four (4) patients served as controls and did not receive any drops. Vitreous (approximately 0.5-1.0 mL) was aspirated prior to opening the infusion line. Specimens were frozen at -68 degrees C until analyzed., Results: In the b.i.d. group, the mean concentration of brimonidine was 16.74 nM+/-10.33 standard deviation (range, 0.42-34.68 nM; median, 16.38); in the t.i.d. group, the mean concentration of brimonidine was 19.16 nM+/-15.40 standard deviation (range, 0.22-39.48 nM; median, 16.98). A significant difference was observed between the (no drug) control vitreous brimonidine levels and b.i.d. or t.i.d. vitreous levels (P<0.01, <0.01, respectively; n=4, 9, and 10, respectively); and in brimonidine levels between t.i.d. phakic patients and t.i.d. patients with posterior chamber lens (P=0.04; n=4 and 6, respectively)., Conclusions: Brimonidine-Purite 0.15%, topically applied b.i.d. or t.i.d. for 2 weeks prior to collection, acquired vitreous levels of brimonidine at or above the 2-nM concentration known to activate the neuroprotective alpha-2 receptor in animals.
- Published
- 2006
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