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Self-Assembling Peptides: From Design to Biomedical Applications
被引:50
|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
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.
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页数:23
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