原位
催化作用
光动力疗法
肿瘤缺氧
活性氧
肿瘤微环境
化学
光化学
生物物理学
癌症研究
放射治疗
生物
肿瘤细胞
生物化学
有机化学
医学
内科学
作者
Yiyan Yin,Xiyang Ge,Jin Ouyang,Na Na
标识
DOI:10.1038/s41467-024-46987-1
摘要
Abstract Single-atom catalysts (SACs) have attracted interest in photodynamic therapy (PDT), while they are normally limited by the side effects on normal tissues and the interference from the Tumor Microenvironment (TME). Here we show a TME-activated in situ synthesis of SACs for efficient tumor-specific water-based PDT. Upon reduction by upregulated GSH in TME, C 3 N 4 -Mn SACs are obtained in TME with Mn atomically coordinated into the cavity of C 3 N 4 nanosheets. This in situ synthesis overcomes toxicity from random distribution and catalyst release in healthy tissues. Based on the Ligand-to-Metal charge transfer (LMCT) process, C 3 N 4 -Mn SACs exhibit enhanced absorption in the red-light region. Thereby, a water-splitting process is induced by C 3 N 4 -Mn SACs under 660 nm irradiation, which initiates the O 2 -independent generation of highly toxic hydroxyl radical (·OH) for cancer-specific PDT. Subsequently, the ·OH-initiated lipid peroxidation process is demonstrated to devote effective cancer cell death. The in situ synthesized SACs facilitate the precise cancer-specific conversion of inert H 2 O to reactive ·OH, which facilitates efficient cancer therapy in female mice. This strategy achieves efficient and precise cancer therapy, not only avoiding the side effects on normal tissues but also overcoming tumor hypoxia.
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