Sun Panpan, Jia Le, Hai Jun, Lu Siyu, Chen Fengjuan, Liang Kun, Sun Shihao, Liu Hanwen, Fu Xu, Zhu Yanhong, Wang Baodui
State Key Laboratory of Applied Organic Chemistry, Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province, Lanzhou University, Gansu, Lanzhou, 730000, China.
College of Life Science and Technology, National Engineering Research Center for Nanomedicine, Huazhong University of Science and Technology, Wuhan, 430074, P. R. China.
Adv Healthc Mater. 2021 Apr;10(7):e2001728. doi: 10.1002/adhm.202001728. Epub 2020 Dec 11.
Carbon monoxide (CO) as an emerging treatment holds great promise for inducing the apoptosis of cancer cells. Here coordination assembled strategy is first reported for synthesis of Cu(II)-flavone coordination polymer (NCu-FleCP) CO nanoprodrug that is stable in normal physiological conditions, and yet readily reduces to small size prodrug complex and releases CO on demand under glutathione (GSH) and near infrared (NIR) light. Specifically, after uptaking by cancer cells, local GSH attacked coordination bond within NCu-FleCP, resulting in the release of Cu(I) and free Fle. The CC bond of Fle is cleavage under NIR light to release CO for gas therapy, and Cu(I) reacts with local H O through Fenton like reaction to generate hydroxyl radicals ( OH) for chemodynamic therapy. Detailed in vitro and in vivo experiments demonstrate that the CO prodrug system in generating a sufficient quantity of CO and OH offers remarkable destructive effects against cancer cells without causing toxicity to surrounding normal tissues. The study provides a solid foundation to develop smart coordination polymer CO prodrugs with on-demand CO release, enhanced permeability and retention effect, and biodegradability for multimodal synergistic therapy.
一氧化碳(CO)作为一种新兴的治疗手段,在诱导癌细胞凋亡方面具有巨大潜力。本文首次报道了通过配位组装策略合成铜(II)-黄酮配位聚合物(NCu-FleCP)CO纳米前药,该前药在正常生理条件下稳定,但在谷胱甘肽(GSH)和近红外(NIR)光作用下可迅速还原为小尺寸前药复合物并按需释放CO。具体而言,癌细胞摄取后,局部GSH攻击NCu-FleCP内的配位键,导致Cu(I)和游离黄酮释放。黄酮的CC键在近红外光下断裂释放CO用于气体治疗,Cu(I)通过类芬顿反应与局部H₂O反应生成羟基自由基(·OH)用于化学动力治疗。详细的体外和体内实验表明,该CO前药系统能产生足够量的CO和·OH,对癌细胞具有显著的破坏作用,且不会对周围正常组织造成毒性。该研究为开发具有按需释放CO、增强的渗透和滞留效应以及可生物降解性的智能配位聚合物CO前药用于多模式协同治疗提供了坚实基础。