Cyanine-Flavonol Hybrids for Near-Infrared Light-Activated Delivery of Carbon Monoxide

被引:40
|
作者
Stackova, Lenka [1 ,2 ]
Russo, Marina [1 ,2 ]
Muchova, Lucie [3 ,4 ,5 ]
Orel, Vojtech [1 ,2 ]
Vitek, Libor [3 ,4 ,5 ]
Stacko, Peter [1 ,2 ]
Klan, Petr [1 ,2 ]
机构
[1] Masaryk Univ, Fac Sci, Dept Chem, Kamenice 5, Brno 62500, Czech Republic
[2] Masaryk Univ, Fac Sci, RECETOX, Kamenice 5, Brno 62500, Czech Republic
[3] Charles Univ Prague, Inst Med Biochem, Bojisti 3, Prague 12108 2, Czech Republic
[4] Charles Univ Prague, Gen Fac Hosp, Lab Diagnost, Bojisti 3, Prague 12108 2, Czech Republic
[5] Charles Univ Prague, Fac Med 1, Bojisti 3, Prague 12108 2, Czech Republic
基金
欧盟地平线“2020”;
关键词
CO release; cyanine; near-infrared light; photoCORM; photorelease; MOLECULES; PHOTODECARBONYLATION; CHEMISTRY; CANCER; CHAIN; ACID; DYES;
D O I
10.1002/chem.202003272
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbon monoxide (CO) is an endogenous signaling molecule that controls a number of physiological processes. To circumvent the inherent toxicity of CO, light-activated CO-releasing molecules (photoCORMs) have emerged as an alternative for its administration. However, their wider application requires photoactivation using biologically benign visible and near-infrared (NIR) light. In this work, a strategy to access such photoCORMs by fusing two CO-releasing flavonol moieties with a NIR-absorbing cyanine dye is presented. These hybrids liberate two molecules of CO in high chemical yields upon activation with NIR light up to 820 nm and exhibit excellent uncaging cross-sections, which surpass the state-of-the-art by two orders of magnitude. Furthermore, the biocompatibility and applicability of the system in vitro and in vivo are demonstrated, and a mechanism of CO release is proposed. It is hoped that this strategy will stimulate the discovery of new classes of photoCORMs and accelerate the translation of CO-based phototherapy into practice.
引用
收藏
页码:13184 / 13190
页数:7
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