药物输送
生物相容性
淀粉样纤维
纳米技术
靶向给药
免疫疗法
药品
淀粉样蛋白(真菌学)
药物开发
脂质体
毒品携带者
化学
药物发现
免疫系统
生物相容性材料
组织工程
纳米医学
输送系统
疾病治疗
小分子
抗原呈递
药理学
医学
作者
Brianna McVay,Dana Wolfe,Ayyalusamy Ramamoorthy
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-09-17
卷期号:41 (38): 25849-25867
被引量:5
标识
DOI:10.1021/acs.langmuir.5c03238
摘要
Self-assembly of molecules is increasingly utilized in the design and development of novel materials for various chemical and biomedical applications. Amyloid fibrils, traditionally associated with neurodegenerative diseases, make up a class of biomaterials formed through the self-assembly of peptides and proteins. The excellent stability and biocompatibility of cross-β-sheet nanostructured amyloid fibrils make them promising biomaterials for therapeutic delivery and immunomodulation. Recent studies have demonstrated the ability of amyloid fibrils to encapsulate small molecules, support receptor-specific targeting through surface functionalization, and enable environmentally responsive drug release. Amyloid-based scaffolds have also shown notable potential in vaccine development and the controlled delivery of checkpoint inhibitors. Current research aims to hybridize amyloid-based scaffolds with commonly used drug delivery tools, such as liposomes and hydrogels, to further enhance therapeutic efficacy while minimizing toxicity. In immunological applications, amyloid fibrils serve as both carriers and adjuvants, promoting antigen presentation and sustained immune activation. This review provides an overview of current progress in the design and application of functional amyloid nanostructures for targeted drug delivery and immunotherapy. The growing understanding of engineered amyloid-based drug delivery platforms may drive the development of precision medicine and support the design of innovative biomaterials.
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