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用于布林佐胺和噻吗洛尔联合给药的局部用凝胶/微球滴眼液:与传统滴眼液在兔体内的对比研究

Topical Gel/Microsphere Eyedrop for Combined Delivery of Brimonidine and Timolol: A Comparative Study With Traditional Eye Drops in Rabbits.

作者信息

Fan Xin, Harding Phillip A, Ziaei Parissa, Chaudhry Ahmad B, West Raymond E, Nolin Thomas D, DiLeo Morgan V

机构信息

Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA, USA.

Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Transl Vis Sci Technol. 2025 Jul 1;14(7):15. doi: 10.1167/tvst.14.7.15.

Abstract

PURPOSE

Topical eye drops combining multiple antiglaucoma agents are often required when monotherapy fails to reduce intraocular pressure (IOP). However, their effectiveness is compromised by low bioavailability and poor patient compliance. To address these issues, we developed a novel gel/microsphere eye drop (GME) containing brimonidine and timolol, aimed at enhancing ocular bioavailability, reducing dosing frequency, and improving patient compliance.

METHODS

The GME system comprises separate formulations of brimonidine-loaded and timolol-loaded polymer microspheres within a thermoresponsive hydrogel, enabling simple off-the-shelf preparation. We examined the in vitro drug release, compared the biodistribution with traditional eye drops, and assessed pharmacodynamic effects in New Zealand white rabbits and Dutch Belted rabbits.

RESULTS

Brimonidine and timolol reached high concentrations in the aqueous and vitreous humor at 1 hour following eye drop administration, declining to nearly undetectable levels by 24 hours. The GME system at a similar dose extended the drug release to 27 days with initially lower drug levels but decreasing more slowly. The GME system also resulted in significantly lower plasma drug concentrations than eye drops, suggesting a reduced risk of systemic side effects. Neither the GME nor eye drops significantly reduced IOP in normotensive rabbits.

CONCLUSIONS

The GME system presents a promising alternative to traditional eye drops for controlled drug release in ocular applications, enabling sustained drug delivery while minimizing systemic exposure and thereby potentially enhancing the safety and efficacy of ocular therapies.

TRANSLATIONAL RELEVANCE

The GME system bridges basic research and clinical application by providing a controlled-release platform that sustains drug delivery, reduces systemic side effects, and enhances patient adherence.

摘要

目的

当单一疗法无法降低眼压(IOP)时,通常需要联合多种抗青光眼药物的局部滴眼剂。然而,它们的有效性因生物利用度低和患者依从性差而受到影响。为了解决这些问题,我们开发了一种含有溴莫尼定和噻吗洛尔的新型凝胶/微球滴眼剂(GME),旨在提高眼部生物利用度、减少给药频率并改善患者依从性。

方法

GME系统由热响应水凝胶中分别装载溴莫尼定和噻吗洛尔的聚合物微球制剂组成,便于现成制备。我们研究了体外药物释放,将其生物分布与传统滴眼剂进行比较,并评估了在新西兰白兔和荷兰带兔中的药效学作用。

结果

滴眼给药1小时后,溴莫尼定和噻吗洛尔在房水和玻璃体液中达到高浓度,到24小时时降至几乎检测不到的水平。相似剂量的GME系统将药物释放延长至27天,初始药物水平较低但下降更缓慢。GME系统还导致血浆药物浓度明显低于滴眼剂,表明全身副作用风险降低。GME和滴眼剂均未显著降低正常血压兔的眼压。

结论

GME系统为眼部应用中的药物控释提供了一种有前景的传统滴眼剂替代方案,能够实现持续药物递送,同时最小化全身暴露,从而潜在地提高眼部治疗的安全性和有效性。

转化相关性

GME系统通过提供一个控释平台来弥合基础研究与临床应用之间的差距,该平台可维持药物递送、减少全身副作用并提高患者依从性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917e/12302038/6239ce50d1dc/tvst-14-7-15-f001.jpg

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