谷胱甘肽
氧化还原
活性氧
化学
卟啉
金属有机骨架
生物物理学
荧光
光化学
生物化学
无机化学
有机化学
生物
物理
吸附
酶
量子力学
作者
Shuangshuang Wan,Cheng Qian,Xuan Zeng,Xian‐Zheng Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2019-05-28
卷期号:13 (6): 6561-6571
被引量:251
标识
DOI:10.1021/acsnano.9b00300
摘要
Here, a Mn(III)-sealed metal–organic framework (MOF) nanosystem based on coordination between Mn(III) and porphyrin (TCPP) via a one-pot method was designed and constructed. Mn(III), as a sealer, not only quenched TCPP-based fluorescence but also inhibited reactive oxygen species (ROS) generation, which made MOFs an "inert" theranostic nanoparticle. Interestingly, upon endocytosis by tumor cells, MOFs were disintegrated into Mn(II) and free TCPP by intracellular glutathione (GSH) in tumor cells, owing to redox reaction between Mn(III) and GSH. This disintegration would lead to consumption of antioxidant GSH and activated Mn(II)-based magnetic resonance imaging (MRI) as well as TCPP-based fluorescent imaging. More importantly, such a GSH-regulated TCPP release could implement controllable ROS generation under irradiation, which avoided side effects (inflammation and damage of normal tissues). As a consequence, after unlocking by GSH, Mn(III)-sealed MOFs could significantly improve the therapeutic efficiency of photodynamic therapy by combining controlled ROS generation and GSH depletion after precise dual tumor homing.
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