Harnessing the Therapeutic Potential of Biomacromolecules through Intracellular Delivery of Nucleic Acids, Peptides, and Proteins

被引:33
|
作者
Tian, Yu [1 ]
Tirrell, Matthew, V [1 ]
LaBelle, James L. [2 ]
机构
[1] Univ Chicago, Pritzker Sch Mol Engn, 5640 S Ellis Ave, Chicago, IL 60637 USA
[2] Univ Chicago, Sect Hematol Oncol, Dept Pediat, 900 E 57th St, Chicago, IL 60637 USA
关键词
biological drugs; drug delivery; intracellular targets; nanomedicines; CELL-PENETRATING PEPTIDES; MURAMYL TRIPEPTIDE PHOSPHATIDYLETHANOLAMINE; RECEPTOR-MEDIATED ENDOCYTOSIS; PERMEABLE MINIATURE PROTEINS; IN-VIVO; LIPID NANOPARTICLES; MESSENGER-RNA; ADENOASSOCIATED VIRUS; CYTOSOLIC DELIVERY; STAPLED PEPTIDE;
D O I
10.1002/adhm.202102600
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Biomacromolecules have long been at the leading edge of academic and pharmaceutical drug development and clinical translation. With the clinical advances of new therapeutics, such as monoclonal antibodies and nucleic acids, the array of medical applications of biomacromolecules has broadened considerably. A major on-going effort is to expand therapeutic targets within intracellular locations. Owing to their large sizes, abundant charges, and hydrogen-bond donors and acceptors, advanced delivery technologies are required to deliver biomacromolecules effectively inside cells. In this review, strategies used for the intracellular delivery of three major forms of biomacromolecules: nucleic acids, proteins, and peptides, are highlighted. An emphasis is placed on synthetic delivery approaches and the major hurdles needed to be overcome for their ultimate clinical translation.
引用
收藏
页数:26
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