Design of biomaterials for intracellular delivery of carbon monoxide

被引:66
作者
Inaba, Hiroshi [1 ]
Fujita, Kenta [2 ]
Ueno, Takafumi [2 ]
机构
[1] Univ Illinois, Roger Adams Lab, Dept Chem, Urbana, IL 61801 USA
[2] Tokyo Inst Technol, Grad Sch Biosci & Biotechnol, Dept Biomol Engn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
关键词
CO-RELEASING MOLECULES; ET-CORMS; TRICARBONYL COMPLEXES; DRUG-DELIVERY; VISIBLE-LIGHT; MANGANESE CARBONYLS; BIOLOGICAL TARGETS; ENZYME; PHOTOCORM; NANOPARTICLES;
D O I
10.1039/c5bm00210a
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Carbon monoxide (CO) is recognized as one of the most important gas signaling molecules involved in governing various therapeutic responses. Intracellular generation of CO is spatiotemporally controlled by catalytic reactions of heme oxygenases (HOs). Thus, the ability to control intracellular CO delivery with modulation of the CO-release rate in specific amounts and locations is expected to improve our fundamental understanding of the functions of CO and the development of clinical applications. For this purpose, CO-releasing molecules (CORMs) have been developed and investigated in vitro and in vivo. Most CORMs are based on transition metal carbonyl complexes. Recently, various biomaterials consisting of metal carbonyls with biomacromolecular scaffolds have been reported to improve the properties of bare metal carbonyls. In this mini-review, current progress in CO delivery, recent strategies for the development of CORMs, and future directions in this field are discussed.
引用
收藏
页码:1423 / 1438
页数:16
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