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Self-assembled single-atom nanozyme for enhanced photodynamic therapy treatment of tumor

机译:用于增强光动力治疗肿瘤的自组装单原子纳佐

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Hypoxia of solid tumor compromises the therapeutic outcome of photodynamic therapy (PDT) that relies on localized O 2 molecules to produce highly cytotoxic singlet oxygen ( 1 O 2 ) species. Herein, we present a safe and versatile self-assembled PDT nanoagent, i.e., OxgeMCC-r single-atom enzyme (SAE), consisting of single-atom ruthenium as the?active catalytic site anchored in a metal-organic framework Mn 3 [Co(CN) 6 ] 2 with encapsulated chlorin e6 (Ce6), which serves as a catalase-like nanozyme for oxygen generation. Coordination-driven self-assembly of organic linkers and metal ions in the presence of a biocompatible polymer generates a nanoscale network that adaptively encapsulates Ce6. The resulted OxgeMCC-r SAE possesses well-defined morphology, uniform size distribution and high loading capacity. When conducting the in situ O 2 generation through the reaction between endogenous H 2 O 2 and single-atom Ru species of OxgeMCC-r SAE, the hypoxia in tumor microenvironment is relieved. Our study demonstrates a promising self-assembled nanozyme with highly efficient single-atom catalytic sites for cancer treatment.
机译:固体肿瘤的缺氧损害了依赖于局部O 2分子的光动力治疗(PDT)的治疗结果,以产生高细胞毒性单态氧(1 o 2)物种。在此,我们介绍了一种安全且通用的自组装的PDT纳米 - 纳代,即Oxgemcc-R单原子酶(SAE),其由单原子钌组成,作为锚定的α-活性催化位点,其固定在金属有机框架Mn 3中[Co (CN)6] 2用封装的氯丙烯E6(CE6),其用作氧化酶状纳佐的氧化酶。在生物相容性聚合物存在下的有机连接剂和金属离子的协调驱动的自组装产生了一种自适应封装CE6的纳米级网络。得到的oxgemcc-r sae具有明确定义的形态,均匀的尺寸分布和高负载能力。当通过内源H 2 O 2和Oxgemcc-R Sae的单源H 2 O 2和单射脉Ru种的反应进行原位O 2时,肿瘤微环境中的缺氧被释放。我们的研究表明,具有高效单原子催化部位的有前途的自组装纳佐,用于癌症治疗。

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