Peptide-based delivery of therapeutics in cancer treatment

被引:51
作者
Samec, Timothy [1 ]
Boulos, Jessica [1 ]
Gilmore, Serena [1 ]
Hazelton, Anthony [1 ]
Alexander-Bryant, Angela [1 ,2 ]
机构
[1] Clemson Univ, Dept Bioengn, Nanobiotechnol Lab, Clemson, SC USA
[2] Rhodes Engn Res Ctr, 301 Engn Serv Dr, Clemson, SC 29631 USA
基金
美国国家科学基金会; 芬兰科学院;
关键词
Peptide delivery; Nanoparticle conjugation; Gene therapy; Drug therapy; Cancer; CELL-PENETRATING PEPTIDE; RECEPTOR-BINDING PEPTIDES; FUSION PEPTIDE; DRUG-DELIVERY; ENDOSOMAL ESCAPE; PHAGE DISPLAY; IN-VITRO; MEMBRANE-FUSION; SIRNA DELIVERY; OVARIAN-CANCER;
D O I
10.1016/j.mtbio.2022.100248
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Current delivery strategies for cancer therapeutics commonly cause significant systemic side effects due to required high doses of therapeutic, inefficient cellular uptake of drug, and poor cell selectivity. Peptide-based delivery systems have shown the ability to alleviate these issues and can significantly enhance therapeutic loading, delivery, and cancer targetability. Peptide systems can be tailor-made for specific cancer applications. This review describes three peptide classes, targeting, cell penetrating, and fusogenic peptides, as stand-alone nanoparticle systems, conjugations to nanoparticle systems, or as the therapeutic modality. Peptide nanoparticle design, characteristics, and applications are discussed as well as peptide applications in the clinical space.
引用
收藏
页数:17
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