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用于阿尔茨海默病靶向治疗的基于细胞原代的仿生纳米材料。

Cell primitive-based biomimetic nanomaterials for Alzheimer's disease targeting and therapy.

作者信息

Yin Tong, Liu Yan, He Bin, Gong Baofeng, Chu Jianjian, Gao Chao, Liang Wendanqi, Hao Mengqi, Sun Wenjing, Zhuang Jianhua, Gao Jie, Yin You

机构信息

Department of Neurology, Second Affiliated Hospital of Naval Medical University (Shanghai Changzheng Hospital), Shanghai, 200003, China.

Department of Clinical Pharmacy, Xinhua Hospital, Clinical pharmacy innovation institute, Shanghai Jiao Tong University of Medicine, Shanghai, 200000, China.

出版信息

Mater Today Bio. 2023 Sep 1;22:100789. doi: 10.1016/j.mtbio.2023.100789. eCollection 2023 Oct.

Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disorder, which is not just confined to the older population. Although developments have been made in AD treatment, various limitations remain to be addressed. These are partly contributed by biological hurdles, such as the blood-brain barrier and peripheral side effects, as well as by lack of carriers that can efficiently deliver the therapeutics to the brain while preserving their therapeutic efficacy. The increasing AD prevalence and the unavailability of effective treatments have encouraged researchers to develop improved, convenient, and affordable therapies. Functional materials based on primitive cells and nanotechnology are emerging as attractive therapeutics in AD treatment. Cell primitives possess distinct biological functions, including long-term circulation, lesion site targeting, and immune suppression. This review summarizes the challenges in the delivery of AD drugs and recent advances in cell primitive-based materials for AD treatment. Various cell primitives, such as cells, extracellular vesicles, and cell membranes, are presented together with their distinctive biological functions and construction strategies. Moreover, future research directions are discussed on the basis of foreseeable challenges and perspectives.

摘要

阿尔茨海默病(AD)是一种进行性神经退行性疾病,并不局限于老年人群体。尽管在AD治疗方面已取得进展,但仍有各种局限性有待解决。这些局限性部分归因于生物障碍,如血脑屏障和外周副作用,以及缺乏能够在保持治疗效果的同时将治疗药物有效递送至大脑的载体。AD患病率的不断上升以及有效治疗方法的缺乏,促使研究人员开发改进的、方便且负担得起的疗法。基于原始细胞和纳米技术的功能材料正成为AD治疗中具有吸引力的治疗手段。原始细胞具有独特的生物学功能,包括长期循环、损伤部位靶向和免疫抑制。本文综述了AD药物递送中的挑战以及基于原始细胞的材料在AD治疗中的最新进展。介绍了各种原始细胞,如细胞、细胞外囊泡和细胞膜,以及它们独特的生物学功能和构建策略。此外,基于可预见的挑战和前景,讨论了未来的研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12c7/10495673/b5b065f230c9/ga1.jpg

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