Graduate Institute of Biomedical Engineering, Chang Gung University, Taoyuan 33302, Taiwan, ROC.
Graduate Institute of Biomedical Engineering, Chang Gung University, Taoyuan 33302, Taiwan, ROC; Department of Ophthalmology, Chang Gung Memorial Hospital, Linkou, Taoyuan 33305, Taiwan, ROC; Department of Materials Engineering, Ming Chi University of Technology, New Taipei City 24301, Taiwan, ROC.
Mater Sci Eng C Mater Biol Appl. 2020 Oct;115:111095. doi: 10.1016/j.msec.2020.111095. Epub 2020 May 14.
Dry eye disease (DED) is the most common ocular disorder that causes persistent discomfort and blurry vision in patients. Despite pharmacotherapy strategies, the current topical administration of eye drops remains a great challenge owing to their low bioavailability and short residence time. Herein, we demonstrate an effective topical treatment of DED via rational design of a long-acting and mucoadhesive drug delivery system. Specifically, the drug carrier is a chemically ternary material system consisting of gelatin that serves as an enzyme-mediated degradable matrix, poly(N-isopropylacrylamide) as a thermo-responsive regulator, and lectin Helix pomatia agglutinin as a mucus-binding component. The long-acting drug release performance is exploited via initiator effects during the synthesis of the thermo-responsive polymer, while the mucoadhesive feature is inherited from the mucus-binding material. In a rabbit model of DED, a pharmacotherapy based on one-time topical administration of epigallocatechin gallate-loaded carrier onto the cul-de-sac could effectively repair the defective corneal epithelium via mitigating cellular inflammation, oxidative stress, and cell apoptosis for a sustained period over 14 days. These findings on the initiator and synergy effects in the development of the advanced ophthalmic formulation show great promise for efficient management of complex ocular diseases by a simple topical administration route.
干眼症(DED)是最常见的眼部疾病,会导致患者持续不适和视力模糊。尽管有药物治疗策略,但由于眼用制剂的生物利用度低和驻留时间短,目前的局部给药仍然是一个巨大的挑战。在此,我们通过合理设计长效和黏膜黏附性药物传递系统,展示了一种有效的 DED 局部治疗方法。具体而言,药物载体是一种化学三元材料系统,由明胶作为酶介导可降解基质、聚(N-异丙基丙烯酰胺)作为温敏调节剂和凝集素 Helix pomatia agglutinin 作为黏液结合成分组成。通过在温敏聚合物合成过程中的引发剂效应来实现长效药物释放性能,而黏膜黏附特性则来自于黏液结合材料。在 DED 的兔模型中,基于姜黄素载药载体一次性局部给药的药物治疗可以通过减轻细胞炎症、氧化应激和细胞凋亡,在 14 天以上的时间内有效修复受损的角膜上皮。这些关于引发剂和协同效应在先进眼科制剂开发中的发现,为通过简单的局部给药途径有效管理复杂眼部疾病提供了巨大的希望。