Jemni-Damer Nahla, Guedan-Duran Atocha, Fuentes-Andion María, Serrano-Bengoechea Nora, Alfageme-Lopez Nuria, Armada-Maresca Felix, Guinea Gustavo V, Pérez-Rigueiro José, Rojo Francisco, Gonzalez-Nieto Daniel, Kaplan David L, Panetsos Fivos
Neuro-Computing and Neuro-Robotics Research Group, Complutense University of Madrid, Madrid, Spain.
Innovation Group, Institute for Health Research San Carlos Clinical Hospital (IdISSC), Madrid, Spain.
Front Bioeng Biotechnol. 2020 Nov 3;8:549089. doi: 10.3389/fbioe.2020.549089. eCollection 2020.
Age-related Macular Degeneration (AMD) is an up-to-date untreatable chronic neurodegenerative eye disease of multifactorial origin, and the main causes of blindness in over 65 years old people. It is characterized by a slow progression and the presence of a multitude of factors, highlighting those related to diet, genetic heritage and environmental conditions, present throughout each of the stages of the illness. Current therapeutic approaches, mainly consisting of intraocular drug delivery, are only used for symptoms relief and/or to decelerate the progression of the disease. Furthermore, they are overly simplistic and ignore the complexity of the disease and the enormous differences in the symptomatology between patients. Due to the wide impact of the AMD and the up-to-date absence of clinical solutions, the development of biomaterials-based approaches for a personalized and controlled delivery of therapeutic drugs and biomolecules represents the main challenge for the defeat of this neurodegenerative disease. Here we present a critical review of the available and under development AMD therapeutic approaches, from a biomaterials and biotechnological point of view. We highlight benefits and limitations and we forecast forthcoming alternatives based on novel biomaterials and biotechnology methods. In the first part we expose the physiological and clinical aspects of the disease, focusing on the multiple factors that give origin to the disorder and highlighting the contribution of these factors to the triggering of each step of the disease. Then we analyze available and under development biomaterials-based drug-delivery devices (DDD), taking into account the anatomical and functional characteristics of the healthy and ill retinal tissue.
年龄相关性黄斑变性(AMD)是一种起源多因素的、目前无法治愈的慢性神经退行性眼病,是65岁以上人群失明的主要原因。其特点是进展缓慢且存在多种因素,突出了与饮食、遗传和环境条件相关的因素,这些因素在疾病的各个阶段都存在。目前的治疗方法主要包括眼内给药,仅用于缓解症状和/或减缓疾病进展。此外,这些方法过于简单,忽视了疾病的复杂性以及患者之间症状的巨大差异。由于AMD的广泛影响以及目前缺乏临床解决方案,开发基于生物材料的方法来个性化和可控地递送治疗药物和生物分子是战胜这种神经退行性疾病的主要挑战。在此,我们从生物材料和生物技术的角度对现有的以及正在开发的AMD治疗方法进行批判性综述。我们强调其优点和局限性,并基于新型生物材料和生物技术方法预测未来的替代方案。在第一部分中,我们阐述了该疾病的生理和临床方面,重点关注引发该疾病的多种因素,并强调这些因素对疾病各阶段触发的作用。然后,我们分析现有的以及正在开发的基于生物材料的药物递送装置(DDD),同时考虑健康和患病视网膜组织的解剖和功能特征。