化学
单线态氧
光热治疗
系统间交叉
光化学
螯合作用
赫拉
细胞毒性
光动力疗法
纳米颗粒
纳米技术
组合化学
吸收(声学)
氧气
单重态
体外
有机化学
生物化学
材料科学
核物理学
激发态
物理
声学
作者
Mingdang Li,Yunjian Xu,Menglong Zhao,Feiyang Li,Wei Feng,Feng Teng,Shujuan Liu,Qiang Zhao
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2020-12-09
卷期号:59 (24): 17826-17833
被引量:11
标识
DOI:10.1021/acs.inorgchem.0c02631
摘要
Pt(II) photosensitizers are emerging as novel Pt anticancer agents for cancer photodynamic therapy (PDT) to avoid uncontrollable toxicity of cisplatin. However, the application of Pt(II) photosensitizers is limited by tumor hypoxia and the poor penetration depth of excitation light. To overcome these drawbacks, exploiting the next generation of Pt anticancer agents is of urgent need. According to theoretical calculations, novel near-infrared (NIR)-absorbing Pt(II)-chelated azadipyrromethene dyes (PtDP-X, where X = N, C, and S) were designed. Importantly, spin–orbit coupling of the Pt atom could promote the intersystem crossing of a singlet-to-triplet transition for converting oxygen to singlet oxygen (1O2), and the azadipyrromethene skeleton could provide a strong photothermal effect. As expected, PtDP-X exhibited intense NIR absorption and synergistic PDT and photothermal effects with low dark cytotoxicity. Furthermore, water-soluble and biocompatible PtDP-N nanoparticles (PtDP-N NPs) were prepared that achieved effective tumor cell elimination with low side effects under 730 nm light irradiation in vitro and in vivo. This pioneering work could push the exploitation of NIR-absorbing metal-chelated azadipyrromethene dyes, so as to promote the positive evolution of phototherapy agents.
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