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Overcoming Endosomal Entrapment in Drug Delivery
被引:267
|作者:
Pei, Dehua
[1
]
Buyanova, Marina
[1
]
机构:
[1] Ohio State Univ, Dept Chem & Biochem, 484 West 12th Ave, Columbus, OH 43210 USA
基金:
美国国家卫生研究院;
关键词:
CELL-PENETRATING PEPTIDES;
INTRACELLULAR DELIVERY;
MAMMALIAN-CELLS;
SIRNA DELIVERY;
PORE FORMATION;
EFFICIENT DELIVERY;
MINIATURE PROTEINS;
PROTON SPONGE;
GENE-TRANSFER;
CALCIUM-IONS;
D O I:
10.1021/acs.bioconjchem.8b00778
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Intracellular delivery of biological agents such as peptides, proteins, and nucleic acids generally rely on the endocytic pathway as the major uptake mechanism, resulting in their entrapment inside the endosome and lysosome. The recent discovery of cell-penetrating molecules of exceptionally high endosomal escape and cytosolic delivery efficiencies and elucidation of their mechanism of action represent major breakthroughs in this field. In this Topical Review, we provide an overview of the recent progress in understanding and enhancing the endosomal escape process and the new opportunities opened up by these recent findings.
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页码:273 / 283
页数:11
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