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Dexamethasone nanowafer as an effective therapy for dry eye disease

地塞米松 眼药水 体内 医学 药理学 加药 促炎细胞因子 角膜 眼科 炎症 化学 内科学 生物 生物技术
作者
Terry G. Coursey,Johanna Tukler Henriksson,Daniela C. Marcano,Crystal S. Shin,Lucas Isenhart,Faheem Ahmed,Cintia S. de Paiva,Stephen C. Pflugfelder,Ghanashyam Acharya
出处
期刊:Journal of Controlled Release [Elsevier BV]
卷期号:213: 168-174 被引量:83
标识
DOI:10.1016/j.jconrel.2015.07.007
摘要

Dry eye disease is a major public health problem that affects millions of people worldwide. It is presently treated with artificial tear and anti-inflammatory eye drops that are generally administered several times a day and may have limited therapeutic efficacy. To improve convenience and efficacy, a dexamethasone (Dex) loaded nanowafer (Dex-NW) has been developed that can release the drug on the ocular surface for a longer duration of time than drops, during which it slowly dissolves. The Dex-NW was fabricated using carboxymethyl cellulose polymer and contains arrays of 500 nm square drug reservoirs filled with Dex. The in vivo efficacy of the Dex-NW was evaluated using an experimental mouse dry eye model. These studies demonstrated that once a day Dex-NW treatment on alternate days during a five-day treatment period was able to restore a healthy ocular surface and corneal barrier function with comparable efficacy to twice a day topically applied dexamethasone eye drop treatment. The Dex-NW was also very effective in down regulating expression of inflammatory cytokines (TNF-α, and IFN-γ), chemokines (CXCL-10 and CCL-5), and MMP-3, that are stimulated by dry eye. Despite less frequent dosing, the Dex-NW has comparable therapeutic efficacy to topically applied Dex eye drops in experimental mouse dry eye model, and these results provide a strong rationale for translation to human clinical trials for dry eye.
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