Self-Assembling Peptides: From Design to Biomedical Applications

被引:78
作者
La Manna, Sara [1 ]
Di Natale, Concetta [2 ,3 ]
Onesto, Valentina [4 ]
Marasco, Daniela [1 ]
机构
[1] Univ Naples Federico II, Dept Pharm, I-80131 Naples, Italy
[2] IIT CRIB, Ist Italiano Tecnol, Largo Barsanti & Matteucci 53, I-80125 Naples, Italy
[3] Univ Napoli Federico II, Ctr Ric Interdipartimentale Biomat CRIB, Piazzale Tecchio 80, I-80125 Naples, Italy
[4] CNR NANOTEC, CNR, Inst Nanotechnol, Via Monteroni,C-O Campus Ecotekne, I-73100 Lecce, Italy
基金
英国科研创新办公室;
关键词
SAPs; self-assembly; drug delivery; tissue regeneration; biomaterials; hydrogel; ENZYME-RESPONSIVE NANOPARTICLES; DRUG-DELIVERY; SUPRAMOLECULAR HYDROGEL; NANOFIBER SCAFFOLD; AMINO-ACIDS; TISSUE; NANOTUBES; LANREOTIDE; DIPHENYLALANINE; BIOMATERIALS;
D O I
10.3390/ijms222312662
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Self-assembling peptides could be considered a novel class of agents able to harvest an array of micro/nanostructures that are highly attractive in the biomedical field. By modifying their amino acid composition, it is possible to mime several biological functions; when assembled in micro/nanostructures, they can be used for a variety of purposes such as tissue regeneration and engineering or drug delivery to improve drug release and/or stability and to reduce side effects. Other significant advantages of self-assembled peptides involve their biocompatibility and their ability to efficiently target molecular recognition sites. Due to their intrinsic characteristics, self-assembled peptide micro/nanostructures are capable to load both hydrophobic and hydrophilic drugs, and they are suitable to achieve a triggered drug delivery at disease sites by inserting in their structure's stimuli-responsive moieties. The focus of this review was to summarize the most recent and significant studies on self-assembled peptides with an emphasis on their application in the biomedical field.
引用
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页数:23
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