Methazolamide 1% in cyclodextrin solution lowers IOP in human ocular hypertension

E. Guomundsdottir, E. Stefansson*, G. Bjarnadottir, J. F. Sigurjonsdottir, G. Guomundsdottir, M. Masson, T. Loftsson

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)

Abstract

Purpose. To formulate aqueous eye drops containing methazolamide 1% in cyclodextrin solution and to evaluate their effect on intraocular pressure (IOP) in a double-blind randomized trial in humans. Methazolamide, a carbonic anhydrase inhibitor (CAI), has been used in oral doses in the treatment of glaucoma but hitherto has not been successfully formulated in eye drops. In this study the effects of methazolamide are compared with those of dorzolamide (Trusopt). Methods. Methazolamide 1% was formulated in a 2-hydroxypropyl-β-cyclodextrin with hydroxypropyl methylcellulose in aqueous solution. Eight persons with ocular hypertension were treated with the methazolamide-cyclodextrin eye drops and eight persons with dorzolamide (Trusopt), both groups at dosages of three times a day for 1 week. IOP was measured before treatment was begun and on days 1, 3, and 8 at 9 AM (peak) and 3 PM (trough). Results. After 1 week of treatment, the peak IOP in the methazolamide group had decreased from 24.4 ± 2.1 mm Hg (mean ± SD) to 21.0 ± 2.0 mm Hg, which is a 14% pressure decrease (P = 0.006). In the dorzolamide group, the peak IOP decreased from 23.3 ± 2.1 mm Hg to 17.2 ± 3.1 mm Hg, which is a 26% pressure decrease (P < 0.001). On average, the IOP declined 3.4 ± 1.8 mm Hg after methazolamide administration and 6.1 ± 3.6 mm Hg after dorzolamide. Conclusions. Through cyclodextrin complexation, it is possible to produce topically active methazolamide eye drops that lower IOP. This is the first double-blind clinical trial that demonstrates the efficacy of the classic CAIs in eye drop formulation.

Original languageEnglish
Pages (from-to)3552-3554
Number of pages3
JournalInvestigative Ophthalmology and Visual Science
Volume41
Issue number11
Publication statusPublished - 2000

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