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从结膜囊插入物中持续释放溴莫尼定以降低青光眼治疗的眼内压。

Sustained release of brimonidine from conjunctival sac insert to reduce intraocular pressure for glaucoma treatment.

机构信息

Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Shanghai Medical College, Fudan University; NHC Key Laboratory of Myopia (Fudan University); Key Laboratory of Myopia, Chinese Academy of Medical Sciences; Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China.

Department of Ophthalmology, General Hospital of Ningxia Medical University, Yinchuan, Ningxia, China.

出版信息

Expert Opin Drug Deliv. 2024 Jun;21(6):975-986. doi: 10.1080/17425247.2024.2378082. Epub 2024 Jul 16.

Abstract

BACKGROUND

Glaucoma is one of the major irreversible blinding eye diseases in the world. Reducing intraocular pressure (IOP) is the primary treatment option, and taking eye drops daily is the common method. However, short drug duration and poor bioavailability of eye drops may lead to unsatisfied therapeutic effects and inadequate patient compliance.

METHODS

A brimonidine-loaded silicone rubber insert (BRI@SR@PT) was prepared by loading brimonidine into a surface-modified silicone rubber ring, followed by polydopamine/thermoplastic polyurethane coatings. The physical properties, cytocompatibility and drug release of BRI@SR@PT were investigated. The BRI@SR@PT was administrated in the conjunctival sac of rabbit eyes, and its drug release, IOP-lowering efficacy and biosafety were assessed.

RESULTS

The BRI@SR@PT presented great thermal stability and excellent elasticity. The BRI@SR@PT was able to release BRI sustainably for 28 days with little toxicity . Compared to BRI eye drops, the BRI@SR@PT effectively lowered IOP for 21 days based on the sustained BRI release with great biosafety when administrated in conjunctival sac of rabbit eyes in a noninvasive fashion.

CONCLUSIONS

The conjunctival sac insert (BRI@SR@PT), as a promising drug-delivery platform, may provide a sustained IOP-lowering treatment for patients with ocular hypertension or glaucoma, without the need for invasive procedures.

摘要

背景

青光眼是全球主要的不可逆致盲眼病之一。降低眼内压(IOP)是主要的治疗选择,每天滴眼是常见的方法。然而,滴眼持续时间短和生物利用度差可能导致治疗效果不满意和患者依从性不足。

方法

通过将溴莫尼定载入表面改性的硅橡胶环中,再进行聚多巴胺/热塑性聚氨酯涂层,制备了载溴莫尼定的硅橡胶植入物(BRI@SR@PT)。研究了 BRI@SR@PT 的物理性质、细胞相容性和药物释放。将 BRI@SR@PT 植入兔眼结膜囊,评估其药物释放、降眼压效果和生物安全性。

结果

BRI@SR@PT 具有良好的热稳定性和优异的弹性。BRI@SR@PT 能够持续 28 天释放溴莫尼定,且毒性较小。与溴莫尼定滴眼剂相比,BRI@SR@PT 通过持续释放溴莫尼定有效降低眼压 21 天,当以非侵入性方式植入兔眼结膜囊时具有良好的生物安全性。

结论

结膜囊植入物(BRI@SR@PT)作为一种有前途的药物递送平台,可能为眼压升高或青光眼患者提供持续的降眼压治疗,无需进行侵入性手术。

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