光热治疗
肿瘤微环境
材料科学
活性氧
谷胱甘肽
癌症治疗
癌症
癌细胞
荧光寿命成像显微镜
癌症研究
纳米技术
荧光
生物物理学
化学
生物化学
肿瘤细胞
医学
内科学
生物
酶
物理
量子力学
作者
Yulong Bai,Jingjin Zhao,Liangliang Zhang,Shulong Wang,Jing Hua,Shulin Zhao,Hong Liang
标识
DOI:10.1002/adhm.202102759
摘要
Abstract Tumor microenvironment (TME)‐activated cancer imaging and therapy is a key to achieving accurate diagnosis and treatment of cancer and reducing the side effects. Herein, smart near‐infrared carbon dot‐metal organic framework MIL‐100 (Fe) assemblies are constructed to achieve TME‐activated cancer imaging and chemodynamic‐photothermal combined therapy. First, a near‐infrared emission carbon dot (RCDs) is developed using glutathione (GSH) as the precursor. Then, the RCDs@MIL‐100 self‐assemblies are obtained using RCDs, FeCl 3 , and trimesic acid solutions as raw materials. After the RCDs@MIL‐100 enters the TME, a high concentration of GSH reduces Fe 3+ to Fe 2+ and drains the GSH, triggering the collapse of RCDs@MIL‐100 skeleton and the release of RCDs and Fe 2+ , at which time the RCDs fluorescence is restored and in an “on” state to illuminate the tumor cells, which achieved cancer imaging. The released Fe 2+ reacts with H 2 O 2 in the TME to form highly reactive hydroxyl radicals (•OH) by Fenton reaction, which achieves the chemodynamic therapy of tumors. Thus, efficient synergistic chemodynamic‐photothermal dual mode therapy is achieved under fluorescence imaging guidance with TME response.
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