Drug delivery methods for posterior segment disease

被引:74
作者
Hsu, Jason [1 ]
机构
[1] Wills Eye Inst, Retina Serv, Philadelphia, PA 19107 USA
关键词
dexamethasone; drug delivery; fluocinolone acetonide; uveitis;
D O I
10.1097/ICU.0b013e3281108000
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose of review New pharmacotherapies for posterior segment diseases of the eye have been recently introduced which use novel drug delivery methods. the various current and potential future methods will be discussed. Recent findings Drug delivery systems have been developed which can provided controlled release of drug for potentially long periods of time. Ideal candidates for these devices are chronic conditions that require repeated local administration of drug, such as noninfectious intermediate or posterior uveitis neovascular age-related macular degeneration and persistent macular edema due to diabetic retinopathy or venous occlusive disease. Recently Retisert (Bausch & Lomb, Rochester, New York, USA) a nonbiodegradable fluocinolone acetonide implant, was approved for use in noninfectious vitis affecting the posterior segment and is currently in clinical trial for the treatment of macular edema. A biodegradable dexamethasone implant is currently in clinical trials for the treatment of uveitis and diabetic macular edema. Summary With the development of therapeutic agents that require repeated administration comes a need for new strategies to improve safety and maximize efficacy. Novel drug delivery systems involving nonbiodegradable or biodegradable implants microparticulates or nanoparticulates liposomes, or transscleral iontophoresis may provide the solution.
引用
收藏
页码:235 / 239
页数:5
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