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
光学
酶
物理
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
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, FeCl3 , and trimesic acid solutions as raw materials. After the RCDs@MIL-100 enters the TME, a high concentration of GSH reduces Fe3+ to Fe2+ and drains the GSH, triggering the collapse of RCDs@MIL-100 skeleton and the release of RCDs and Fe2+ , at which time the RCDs fluorescence is restored and in an "on" state to illuminate the tumor cells, which achieved cancer imaging. The released Fe2+ reacts with H2 O2 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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