Self-Assembled Peptide Drug Delivery Systems

被引:105
作者
Yang, Jia [1 ,2 ]
An, Hong-Wei [1 ,2 ]
Wang, Hao [1 ,2 ]
机构
[1] Natl Ctr Nanosci & Technol NCNST, CAS Ctr Excellence Nanosci, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
self-assembly; peptide; nanomaterial; drug delivery; nanoparticles; nanofibrils; SUPRAMOLECULAR FILAMENT HYDROGELS; ENZYME-RESPONSIVE NANOPARTICLES; TARGETED DELIVERY; CELL APOPTOSIS; CANCER-CELLS; TUMOR; DOXORUBICIN; PH; BIOMATERIALS; NANOCARRIERS;
D O I
10.1021/acsabm.0c00707
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Over the past several decades, rapid advances have been made in the application of nanomaterials in the biomedical field including bioimaging and drug delivery. Owing to the natural biocompatibility, diverse design, and dynamic self-assembly, peptides can be used as modules to construct self-assembled peptide-based nanomaterials, which have a high potential in reducing drug toxicity, improving drug targeting, and enhancing drug delivery efficiency. In this review, three typical design strategies of self-assembled peptide nanomaterials for drug delivery have been summarized induding ex situ construction, in situ morphological transformation, and in situ construction of peptide drug delivery systems (FDDs). Drugs can be loaded to peptide nanomaterials by physical encapsulation or chemical conjugation methods, showing enhanced retention effects at tumor sites to increase the uptake rate of drugs. Interestingly, drug-free peptide nanomaterials also can be nanomedicines for delivery. These advances implicate the bright prospect of the self-assembled peptide in intelligent nanomedicine and clinical translation.
引用
收藏
页码:24 / 46
页数:23
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