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通过微创给药实现长效释放的抗黄斑变性多功能纳米疗法

Multifunctional Nanotherapeutics with Long-Acting Release against Macular Degeneration by Minimally Invasive Administration.

作者信息

Chang Wanwan, Lv Xinying, Zhu Jiafei, Shen Jing-Jing, Yao Jing, Liu Zhuang, Chen Qian

机构信息

School of Pharmacy, Faculty of Medicine & Macao Institute of Materials Science and Engineering, Macau University of Science and Technology, Macau SAR 999078, China.

Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, Suzhou, Jiangsu 215127, China.

出版信息

ACS Nano. 2024 Jul 17. doi: 10.1021/acsnano.4c04494.

Abstract

Neovascular age-related macular degeneration (AMD), a leading cause of blindness, requires frequent intravitreal injection of antivascular endothelial growth factor (anti-VEGF), which could generate a succession of complications with poor patient compliance. The current VEGF-targeting therapies often fail in half of patients due to the complex pathologic microenvironment of excessive reactive oxygen species (ROS) production, and increased levels of inflammation are accompanied by choroidal neovascularization (CNV). We herein reported multifunctional nanotherapeutics featuring superior antioxidant and anti-inflammation properties that aim to reverse the pathological condition, alongside its strong targeted antiangiogenesis to CNV and its ability to provide long-term sustained bioactive delivery via the minimally invasive subconjunctival injection, so as to achieve satisfactory wet AMD treatment effects. Concretely, the nanomedicine was designed by coencapsulation of astaxanthin (AST), a red pigmented carotenoid known for its antioxidative, anti-inflammatory and antiapoptotic properties, and axitinib (AXI), a small molecule tyrosine kinase inhibitor that selectively targets the vascular epidermal growth factor receptor for antiangiogenesis, into the Food and Drug Administration (FDA) approved poly(lactic--glycolic acid) (PLGA), which forms the nanodrug of PLGA@AST/AXI. Our results demonstrated that a single-dose subconjunctival administration of PLGA@AST/AXI showed a rational synergistic effect by targeting various prevailing risk factors associated with wet AMD, ensuring persistent drug release profiles, maintaining good ocular biocompatibility, and causing no obvious mechanical damage. Such attributes are vital and hold significant potential in treating ocular posterior segment diseases. Moreover, this nanotherapeutic strategy represents a versatile and broad-spectrum nanoplatform, offering a promising alternative for the complex pathological progression of other neovascular diseases.

摘要

新生血管性年龄相关性黄斑变性(AMD)是导致失明的主要原因,需要频繁玻璃体内注射抗血管内皮生长因子(anti-VEGF),这可能会引发一系列并发症且患者依从性差。由于过量活性氧(ROS)产生的复杂病理微环境,目前的VEGF靶向治疗在一半的患者中常常失败,并且炎症水平升高伴随着脉络膜新生血管(CNV)。我们在此报告了具有卓越抗氧化和抗炎特性的多功能纳米疗法,旨在逆转病理状况,同时其对CNV具有强大的靶向抗血管生成作用,并且能够通过微创结膜下注射实现长期持续的生物活性递送,从而达到令人满意的湿性AMD治疗效果。具体而言,该纳米药物是通过将虾青素(AST)和阿西替尼(AXI)共包封到美国食品药品监督管理局(FDA)批准的聚乳酸-乙醇酸共聚物(PLGA)中设计而成,其中虾青素是一种红色类胡萝卜素,以其抗氧化、抗炎和抗凋亡特性而闻名,阿西替尼是一种小分子酪氨酸激酶抑制剂,可选择性靶向血管表皮生长因子受体以进行抗血管生成,由此形成PLGA@AST/AXI纳米药物。我们的结果表明,单剂量结膜下注射PLGA@AST/AXI通过靶向与湿性AMD相关的各种主要危险因素显示出合理的协同作用,确保持续的药物释放曲线,保持良好的眼内生物相容性,并且不会造成明显的机械损伤。这些特性对于治疗眼后段疾病至关重要且具有巨大潜力。此外,这种纳米治疗策略代表了一种通用且广谱的纳米平台,为其他新生血管疾病的复杂病理进展提供了一种有前景的替代方案。

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