Huang Xi, Zhang Li, Fu Yanyan, Zhang Meixia, Yang Qian, Peng Jinrong
Department of Ophthalmology, Research Laboratory of Macular Disease, Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Center of Scientific Research, Chengdu Medical College, Chengdu, Sichuan, China.
Front Bioeng Biotechnol. 2023 May 23;11:1199922. doi: 10.3389/fbioe.2023.1199922. eCollection 2023.
Age-related macular degeneration (AMD) is the predominant threat to human vision and ultimately results in blindness. With the increase in the aging population, it has become a more crucial issue to human health. AMD is a multifactorial disease with the unique feature of uncontrollable angiogenesis during initiation and progression. Although increasing evidence indicates that AMD is largely hereditary, the predominant efficient treatment is antiangiogenesis, which mainly involves VEGF and HIF-α as therapeutic targets. The repeated administration of this treatment over the long term, generally through intravitreal injection, has called for the introduction of long-term drug delivery systems, which are expected to be achieved by biomaterials. However, the clinical results of the port delivery system indicate that the optimization of medical devices toward prolonging the activities of therapeutic biologics in AMD therapy seems more promising. These results indicate that we should rethink the possibility and potential of biomaterials as drug delivery systems in achieving long-term, sustained inhibition of angiogenesis in AMD therapy. In this review, the etiology, categorization, risk factors, pathogenesis, and current clinical treatments of AMD are briefly introduced. Next, the development status of long-term drug delivery systems is discussed, and the drawbacks and shortages of these systems are emphasized. By comprehensively considering the pathological aspect and the recent application of drug delivery systems in AMD therapy, we hope to find a better solution for the further development of long-term therapeutic strategies for AMD.
年龄相关性黄斑变性(AMD)是对人类视力的主要威胁,最终可导致失明。随着老龄化人口的增加,它已成为对人类健康更为关键的问题。AMD是一种多因素疾病,在发病和进展过程中具有不可控血管生成这一独特特征。尽管越来越多的证据表明AMD很大程度上具有遗传性,但主要的有效治疗方法是抗血管生成,其主要涉及将血管内皮生长因子(VEGF)和缺氧诱导因子-α(HIF-α)作为治疗靶点。这种治疗通常通过玻璃体内注射进行长期重复给药,因此需要引入长期药物递送系统,而这有望通过生物材料来实现。然而,端口递送系统的临床结果表明,在AMD治疗中优化医疗设备以延长治疗性生物制剂的活性似乎更具前景。这些结果表明,我们应该重新思考生物材料作为药物递送系统在实现AMD治疗中对血管生成的长期、持续抑制方面的可能性和潜力。在本综述中,简要介绍了AMD的病因、分类、危险因素、发病机制和当前的临床治疗方法。接下来,讨论了长期药物递送系统的发展现状,并强调了这些系统的缺点和不足。通过综合考虑病理方面以及药物递送系统在AMD治疗中的最新应用,我们希望为AMD长期治疗策略的进一步发展找到更好的解决方案。