Department of Biochemical Engineering, School of Chemical Engineering and Technology and Key Laboratory of Systems Bioengineering and Frontiers Science Center for Synthetic Biology (Ministry of Education), Tianjin University, Tianjin 300350, China.
Department of Biology & Guangdong Provincial Key Laboratory of Marine Biotechnology, Institute of Marine Sciences, College of Science, Shantou University, Shantou, Guangdong 515063, China.
Acta Biomater. 2021 Mar 15;123:93-109. doi: 10.1016/j.actbio.2021.01.018. Epub 2021 Jan 16.
The abnormal self-assembly of amyloid-β protein (Aβ) into toxic aggregates is a major pathological hallmark of Alzheimer's disease (AD). Modulation of Aβ fibrillization with pharmacological modalities has become an active field of research, which aims to mitigate Aβ-induced neurotoxicity and ameliorate impaired recognition. Among the various strategies for AD treatment, phototherapy, including photothermal therapy (PTT), photodynamic therapy (PDT), and photoresponsive release systems have attracted increased attention because of the spatiotemporal controllability. Under the irradiation of light, the heat or reactive oxygen species generated by photothermal or photodynamic processes significantly enhances the efficacy of the inhibitor or modulator, and the "caged" drug can be accurately released at the intended site, thus avoiding adverse effects. This review, from a viewpoint of materials, focuses on the recent advances in modulating Aβ aggregation by light that irradiates on the materials that function on modulating Aβ aggregation. Representative examples of PTT, PDT, and photoresponsive drug release systems are discussed in terms of inhibitory mechanism, the unique properties of materials, and the design of modulators. The major challenges of phototherapy against AD are addressed and the promising prospects are proposed. It is concluded that the noninvasive light-assisted approaches will become a promising strategy for intensifying the modulation of Aβ aggregation and thus facilitating AD treatment. STATEMENT OF SIGNIFICANCE: Alzheimer's disease (AD) with the hallmark of amyloid-β protein (Aβ) deposition is affecting more than 50 million people globally. It is urgent to explore intelligent materials to modulate Aβ aggregation. This review summarizes the intensified modulation of Aβ aggregation by a variety of photoresponsive materials including photothermal, photosensitizing and photoresponsive release materials, focusing on their characteristics and functionalities. We believe this review would arouse more interest in the research field of stimuli-responsive materials and promote their clinical applications in AD therapy.
淀粉样蛋白-β 蛋白 (Aβ) 的异常自组装形成毒性聚集体是阿尔茨海默病 (AD) 的主要病理标志。用药理学方法调节 Aβ 纤维形成已成为一个活跃的研究领域,旨在减轻 Aβ 诱导的神经毒性和改善受损的识别能力。在 AD 治疗的各种策略中,光疗,包括光热疗法 (PTT)、光动力疗法 (PDT) 和光响应释放系统,由于具有时空可控性而引起了越来越多的关注。在光的照射下,光热或光动力过程产生的热量或活性氧显著增强了抑制剂或调节剂的疗效,并且可以在预期部位准确释放“笼蔽”药物,从而避免不良反应。本综述从材料的角度出发,重点介绍了通过照射在调节 Aβ 聚集的材料上的光来调节 Aβ 聚集的最新进展。根据抑制机制、材料的独特性质和调节剂的设计,讨论了 PTT、PDT 和光响应药物释放系统的代表性实例。讨论了光疗治疗 AD 的主要挑战,并提出了有希望的前景。结论是,非侵入性的光辅助方法将成为增强 Aβ 聚集调节的有前途的策略,从而有助于 AD 的治疗。
以淀粉样蛋白-β 蛋白 (Aβ) 沉积为标志的阿尔茨海默病 (AD) 在全球影响着超过 5000 万人。探索智能材料来调节 Aβ 聚集是当务之急。本综述总结了多种光响应材料(包括光热、光敏和光响应释放材料)对 Aβ 聚集的强化调节,重点介绍了它们的特性和功能。我们相信,这篇综述将引起人们对刺激响应材料研究领域的更多兴趣,并促进它们在 AD 治疗中的临床应用。