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载毛果芸香碱抗氧化功能化可生物降解温敏水凝胶的体内药理学评价在青光眼兔模型中的应用。

In vivo Pharmacological Evaluations of Pilocarpine-Loaded Antioxidant-Functionalized Biodegradable Thermogels in Glaucomatous Rabbits.

机构信息

Department of Mechanical Engineering, University of Texas at Tyler, Tyler TX, 75799, USA.

Department of Chemical and Materials Engineering, Chang Gung University, Taoyuan 33302, Taiwan, ROC.

出版信息

Sci Rep. 2017 Feb 10;7:42344. doi: 10.1038/srep42344.

Abstract

To alleviate oxidative stress-induced ocular hypertension, grafting of antioxidant molecules to drug carriers enables a dual-function mechanism to effectively treat glaucomatous intraocular pressure (IOP) dysregulation. Providing potential application for intracameral administration of antiglaucoma medications, this study, for the first time, aims to examine in vivo pharmacological efficacy of pilocarpine-loaded antioxidant-functionalized biodegradable thermogels in glaucomatous rabbits. A series of gallic acid (GA)-grafted gelatin-g-poly(N-isopropylacrylamide) (GN) polymers were synthesized via redox reactions at 20-50 °C. Our results showed that raising redox radical initiation reaction temperature maximizes GA grafting level, antioxidant activity, and water content at 40 °C. Meanwhile, increase in overall hydrophilicity of GNGA carriers leads to fast polymer degradation and early pilocarpine depletion in vivo, which is disadvantageous to offer necessary pharmacological performance at prolonged time. By contrast, sustained therapeutic drug concentrations in aqueous humor can be achieved for long-term (i.e., 28 days) protection against corneal aberration and retinal injury after pilocarpine delivery using dual-function optimized carriers synthesized at 30 °C. The GA-functionalized injectable hydrogels are also found to contribute significantly to enhancement of retinal antioxidant defense system and preservation of histological structure and electrophysiological function, thereby supporting the benefits of drug-containing antioxidant biodegradable thermogels to prevent glaucoma development.

摘要

为了减轻氧化应激引起的眼内高压,将抗氧化分子嫁接到药物载体上,可以实现双重功能机制,有效地治疗青光眼性眼内压(IOP)失调。本研究首次将载有匹鲁卡品的抗氧化功能化可生物降解温敏水凝胶应用于兔眼青光眼模型,旨在考察其体内药代动力学疗效。通过在 20-50°C 下的氧化还原反应,合成了一系列没食子酸(GA)接枝的明胶-g-聚(N-异丙基丙烯酰胺)(GN)聚合物。研究结果表明,提高氧化还原引发反应温度可以使 GA 接枝水平、抗氧化活性和含水量在 40°C 时达到最大值。同时,GNGA 载体整体亲水性的增加导致体内聚合物快速降解和早期匹鲁卡品耗竭,这不利于在延长时间内提供必要的药理性能。相比之下,使用在 30°C 下合成的优化双重功能载体,可在长达 28 天的时间内持续稳定地向房水中输送药物,从而保护角膜像差和视网膜免受损伤。此外,GA 功能化的可注射水凝胶还可以显著增强视网膜抗氧化防御系统,保持组织结构和电生理功能,从而支持含药抗氧化可生物降解温敏水凝胶在预防青光眼发展方面的优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06dd/5301226/62802998d4c6/srep42344-f1.jpg

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