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一种药物释放接触镜治疗青光眼一个月的体内性能。

In vivo performance of a drug-eluting contact lens to treat glaucoma for a month.

机构信息

Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Boston, MA 02114, USA; David H. Koch Institute for Integrative Cancer Research, 77 Massachusetts Ave, Building 76-66, Massachusetts Institute of Technology, Cambridge, MA 02139, USA; Laboratory for Biomaterials and Drug Delivery, Department of Anesthesiology, Division of Critical Care Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Biomaterials. 2014 Jan;35(1):432-9. doi: 10.1016/j.biomaterials.2013.09.032. Epub 2013 Oct 4.

Abstract

For nearly half a century, contact lenses have been proposed as a means of ocular drug delivery, but achieving controlled drug release has been a significant challenge. We have developed a drug-eluting contact lens designed for prolonged delivery of latanoprost for the treatment of glaucoma, the leading cause of irreversible blindness worldwide. Latanoprost-eluting contact lenses were created by encapsulating latanoprost-poly(lactic-co-glycolic acid) films in methafilcon by ultraviolet light polymerization. In vitro and in vivo studies showed an early burst of drug release followed by sustained release for one month. Contact lenses containing thicker drug-polymer films demonstrated released a greater amount of drug after the initial burst. In vivo, single contact lenses were able to achieve, for at least one month, latanoprost concentrations in the aqueous humor that were comparable to those achieved with topical latanoprost solution, the current first-line treatment for glaucoma. The lenses appeared safe in cell culture and animal studies. This contact lens design can potentially be used as a treatment for glaucoma and as a platform for other ocular drug delivery applications.

摘要

近半个世纪以来,人们一直提议将隐形眼镜作为眼部药物输送的一种手段,但实现药物的控制释放一直是一个重大挑战。我们开发了一种载药隐形眼镜,旨在延长拉坦前列素的释放时间,用于治疗青光眼,这是全球导致不可逆性失明的主要原因。通过紫外线光聚合将拉坦前列素-聚(乳酸-共-乙醇酸)薄膜包埋在甲基丙烯酰胺中,从而制备出载拉坦前列素隐形眼镜。体外和体内研究表明,药物释放存在早期突释,随后持续释放一个月。含有较厚药物-聚合物薄膜的隐形眼镜在初始突释后释放出更多的药物。在体内,单个隐形眼镜至少能够在一个月内使房水中的拉坦前列素浓度达到与局部使用拉坦前列素溶液(目前治疗青光眼的一线药物)相当的水平。该隐形眼镜在细胞培养和动物研究中表现出安全性。这种隐形眼镜设计有可能被用于治疗青光眼,也可以作为其他眼部药物输送应用的平台。

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The stabilization mechanism of latanoprost.拉坦前列素的稳定机制。
Int J Pharm. 2011 May 30;410(1-2):23-30. doi: 10.1016/j.ijpharm.2011.03.006. Epub 2011 Mar 22.
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Contact lenses for drug delivery.用于药物递送的隐形眼镜。
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