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新型半三明治型铑(III)和铱(III)光引发剂用于双重化学和光动力疗法。

Novel half-sandwich rhodium(III) and iridium(III) photosensitizers for dual chemo- and photodynamic therapy.

机构信息

Key Laboratory of Guangxi Key Laboratory of Natural Polymer Chemistry and Physics (Nanning Normal University), Nanning, China.

Chongqing Insistute of Forensic Science, Chongqing, China.

出版信息

Photodiagnosis Photodyn Ther. 2019 Jun;26:448-454. doi: 10.1016/j.pdpdt.2019.04.028. Epub 2019 Apr 30.

Abstract

BACKGROUND AND OBJECTIVE

Photodynamic therapy has emerged as a promising treatment for cancer and other malignancies. Design of photosensitizers with two different action mechanisms may be an essential strategy for the improvement of the efficacy of phototherapeutic drugs. The objective of this study was to evaluate the anticancer photo- and chemocytotoxic effects of the novel half-sandwich rhodium(III) and iridium(III) photosensitizers.

MATERIALS AND METHODS

A series of novel half-sandwich Cp*-Rh(III) and Cp*-Ir(III) complexes containing 9-anthraldehyde thiosemicarbazones, (Cp*)M(L)Cl (M = Rh or Ir, L = 9-anthraldehyde thiosemicarbazones), were compared for cell uptake and photo- and chemocytotoxic effects against human prostate carcinoma (PC3) and human ovarian carcinoma (SKOV3) cell lines.

RESULTS

Cp*-Ir(III) complexes, (Cp*)Ir(L)Cl, showed remarkable phototoxic behavior against human ovarian adenocarcinoma SKOV3 cells (IC = 2.7 and 2.3 μM, respectively, λ > 400 nm), as well as the 7.4 and 5.3-fold lower toxicity in the dark, implying possibility of dual action as chemo- and phototherapeutic agents.

CONCLUSION

The complexes, which present a synergistic effect with good properties of both the Cp*-Rh(III) and Cp*-Ir(III) chemotherapeutic effect and the anthracene photodynamic therapy efficiency, show great potential as a new generation of light activated dual-action anticancer agents for photodynamic therapy.

摘要

背景与目的

光动力疗法已成为癌症和其他恶性肿瘤的一种有前途的治疗方法。设计具有两种不同作用机制的光敏剂可能是提高光疗药物疗效的重要策略。本研究的目的是评估新型半夹心铑(III)和铱(III)光敏剂的抗癌光毒性和化学细胞毒性作用。

材料与方法

一系列新型半夹心 Cp*-Rh(III)和 Cp*-Ir(III)配合物,其中含有 9-蒽醛缩硫代氨基脲,(Cp*-M(L)Cl(M=Rh 或 Ir,L=9-蒽醛缩硫代氨基脲),用于细胞摄取以及对人前列腺癌细胞(PC3)和人卵巢癌细胞(SKOV3)系的光毒性和化学细胞毒性作用进行比较。

结果

Cp*-Ir(III)配合物(Cp*-Ir(L)Cl)对人卵巢腺癌 SKOV3 细胞表现出显著的光毒性行为(IC=2.7 和 2.3μM,分别,λ>400nm),并且在黑暗中毒性低 7.4 和 5.3 倍,这意味着可能作为化学和光疗药物的双重作用。

结论

这些配合物具有 Cp*-Rh(III)和 Cp*-Ir(III)化疗效果以及蒽光动力疗法效率的协同作用,具有良好的性质,显示出作为新一代光激活双重作用抗癌药物用于光动力疗法的巨大潜力。

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