28-day intraocular pressure reduction with a single dose of brimonidine tartrate-loaded microspheres

被引:38
作者
Fedorchak, Morgan V. [1 ,2 ,3 ,4 ,7 ,8 ]
Conner, Ian P. [1 ]
Medina, Carlos A. [1 ]
Wingard, Jeremy B. [1 ]
Schuman, Joel S. [1 ,2 ,3 ,5 ,7 ,8 ]
Little, Steven R. [1 ,4 ,5 ,6 ,7 ,8 ]
机构
[1] Univ Pittsburgh, UPMC Eye Ctr, Sch Med, Dept Ophthalmol, Pittsburgh, PA 15213 USA
[2] UPMC, Louis J Fox Ctr Vision Restorat, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Pittsburgh, PA 15261 USA
[4] Univ Pittsburgh, Swanson Sch Engn, Dept Chem Engn, Pittsburgh, PA 15261 USA
[5] Univ Pittsburgh, Swanson Sch Engn, Dept Bioengn, Pittsburgh, PA 15261 USA
[6] Univ Pittsburgh, Dept Immunol, Pittsburgh, PA 15261 USA
[7] UPMC, McGowan Inst Regenerat Med, Pittsburgh, PA 15260 USA
[8] Univ Pittsburgh, Pittsburgh, PA 15260 USA
关键词
glaucoma; microsphere; controlled release; brimonidine; rabbit; intraocular pressure; polymer; OPEN-ANGLE GLAUCOMA; SUBCONJUNCTIVAL INJECTION; IN-VITRO; INTRAVITREAL IMPLANT; CONTROLLED-RELEASE; OCULAR ABSORPTION; DRUG-DELIVERY; MACULAR EDEMA; UNITED-STATES; RABBIT EYES;
D O I
10.1016/j.exer.2014.06.013
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Treatment of glaucoma by intraocular pressure (IOP) reduction is typically accomplished through the administration of eye drops, the difficult and frequent nature of which contributes to extremely low adherence rates. Poor adherence to topical treatment regimens in glaucoma patients can lead to irreversible vision loss and increased treatment costs. Currently there are no approved treatments for glaucoma that address the inherent inefficiencies in drug delivery and patient adherence. Brimonidine tartrate (BT), a common glaucoma medication, requires dosing every 8-12 h, with up to 97% of patients not taking it as prescribed. This study provides proof-of-principle testing of a controlled release BT formulation. BT was encapsulated in poly(lactic-co-glycolic) acid microspheres and drug release was quantified using UV-Vis spectroscopy. For in vivo studies, rabbits were randomized to receive a single subconjunctival injection of blank (no drug) or BT-loaded microspheres or twice daily topical 0.2% BT drops. The microspheres released an average of 2.1 +/- 0.37 mu g BT/mg microspheres/day in vitro. In vivo, the percent decrease in IOP from baseline was significantly greater in the treated eye for both topical drug and drug-loaded microspheres versus blank microspheres throughout the 4-week study, with no evidence of migration or foreign body response. IOP measurements in the contralateral, untreated eyes also suggested a highly localized effect from the experimental treatment. A treatment designed using the release systems described in this study would represent a vast improvement over the current clinical standard of 56-84 topical doses over 28 days. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:210 / 216
页数:7
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