Vitreous concentration of topically applied brimonidine tartrate 0.2%☆
Presented in part at the American Glaucoma Society, San Antonio, Texas, March 2000.
Received 9 May 2000; accepted 22 November 2000.
Abstract
Objective
To determine the vitreous concentration of brimonidine after topical administration of Alphagan.
Design
Prospective observational case series.
Participants
Eighteen patients scheduled for elective pars plana vitrectomy.
Methods
Brimonidine tartrate, 0.2%, was topically administered twice or three times daily for 4 to 14 days preoperatively in 13 patients. Four patients served as controls, without application of brimonidine. A dry, undiluted vitrectomy specimen obtained intraoperatively was collected, frozen, and sent to an independent bioanalytical facility for quantitative determination of vitreous concentration of brimonidine using gas chromatography/mass spectrometry.
Main outcome measures
The concentration of brimonidine in human vitreous.
Results
All patients treated with brimonidine measured above the lower limit of quantitation with a mean vitreous concentration of 185 ± 500 nM. All patients not treated with brimonidine measured at or below the lower limit of quantitation of 0.05 nM. There was a trend toward higher concentration in patients who were either aphakic or pseudophakic compared with those that were phakic.
Conclusions
Topically applied brimonidine results in vitreous levels at or above 2 nM, the concentration shown to activate α2-receptors.
Manuscript no. 200281.
aStorm Eye Institute, Medical University of South Carolina, Charleston, South Carolina, USA
bOschner Clinic, Department of Ophthalmology, New Orleans, Louisiana, USA