用于顺铂耐药非小细胞肺癌光动力/声动力双重疗法的钌复合物的取代基调制激发三重态和活性。

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
ChemBioChem Pub Date : 2024-11-18 DOI:10.1002/cbic.202400801
Dan-Dan Xie, Xue-Lian Li, Li-Zhen Zeng, Xiaoxia Ren, Dan Zhang, Rong Yang, Feng Gao
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引用次数: 0

摘要

我们设计了六种多吡啶基 Ru(II) 复合物,用于单分子光动力和声动力疗法(PDT/SDT)协同多模式抗癌,治疗顺铂耐药的 NSCLC。它们表现出最低的 3ES 值,具有独特的配体内过渡性质,有利于单线态氧的生成。在 808 纳米激光照射或超声波处理下,单线态氧和超氧阴离子的量子产率都非常显著,并能诱导 A549R 细胞凋亡和铁凋亡。细胞毒性实验清楚地表明了 PDT 和 SDT 的协同效应。研究人员详细探讨了这些复合物的结构与其细胞生物学机制之间的关系。利用单分子增敏剂实现 PDT/SDT 的协同效应,可能会为治疗位于深部和缺氧微环境中的耐药肿瘤提供有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Substituent-Modulated Excited Triplet States and Activities of Ruthenium Complexes for Dual Photodynamic/Sonodynamic Therapy to Cisplatin-Resistant Non-Small Cell Lung Cancer.

Six polypyridyl Ru(II) complexes were designed for single-molecule photodynamic and sonodynamic therapy (PDT/SDT) synergistic multimodal anticancer toward cisplatin-resistant NSCLC. They demonstrated lowest 3ES with distinct intraligand transition nature, which is beneficial for singlet oxygen generation. Remarkable quantum yields of both singlet oxygen and superoxide anion under either 808 nm laser irradiation or ultrasonic treatment and could induce apoptosis and ferroptosis of A549R cells. Cytotoxicity experiments clearly demonstrated a synergistic effect between PDT and SDT. The relationship between the structures of these complexes and their cellular biological mechanisms has been explored in detail. Using a single-molecule sensitizer to achieve synergistic PDT/SDT may provide valuable insights for the treatment of drug-resistant tumors that located deeply and in hypoxic microenvironment.

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来源期刊
ChemBioChem
ChemBioChem 生物-生化与分子生物学
CiteScore
6.10
自引率
3.10%
发文量
407
审稿时长
1 months
期刊介绍: ChemBioChem (Impact Factor 2018: 2.641) publishes important breakthroughs across all areas at the interface of chemistry and biology, including the fields of chemical biology, bioorganic chemistry, bioinorganic chemistry, synthetic biology, biocatalysis, bionanotechnology, and biomaterials. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and supported by the Asian Chemical Editorial Society (ACES).
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