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具有增强光动力疗法活性的绿光激活双功能铂(IV)前药

Green Light Activated Dual-Action Pt(IV) Prodrug with Enhanced PDT Activity.

作者信息

Spector Daniil, Bykusov Vladislav, Isaeva Yulia, Akasov Roman, Zharova Anastasia, Rodin Igor, Vokuev Mikhail, Grishin Yuri, Nikitina Vita, Martynov Alexander, Kuzmin Vladimir, Beloglazkina Elena, Krasnovskaya Olga

机构信息

Chemistry Department, Lomonosov Moscow State University, Leninskie gory 1,3, 119991, Moscow, Russia.

I.M. Sechenov First Moscow State Medical University, Trubetskaya 8-2, Moscow, 119991, Russia.

出版信息

ChemMedChem. 2025 Apr 14;20(8):e202400786. doi: 10.1002/cmdc.202400786. Epub 2025 Feb 9.

Abstract

Light induced release of cisplatin from Pt(IV) prodrugs is a promising tool for precise spatiotemporal control over the antiproliferative activity of Pt-based chemotherapeutic drugs. A combination of light-controlled chemotherapy (PACT) and photodynamic therapy (PDT) in one molecule has the potential to overcome crucial drawbacks of both Pt-based chemotherapy and PDT via a synergetic effect. Herein we report green-light-activated Pt(IV) prodrug GreenPt with BODIPY-based photosentitizer in the axial position with an incredible high light response and singlet oxygen generation ability. GreenPt demonstrated the ability to release cisplatin under low-dose green light irradiation up to 1 J/cm. The investigation of the photoreduction mechanism of GreenPt prodrug using DFT modeling and ΔG PET estimation revealed that the anion-radical formation and substituent photoinduced electron transfer from the triplet excited state of the BODIPY axial ligand to the Pt(IV) center is the key step in the light-induced release of cisplatin. Green-light-activated BODIPY-based photosentitizers 5 and 8 demonstrated outstanding photosensitizing properties with an extraordinary phototoxicity index (PI)>1300. GreenPt prodrug demonstrated gradual intracellular accumulation and light-induced phototoxicity with PI>100, thus demonstrating dual action through light-controlled release of both cisplatin and a potent BODIPY-based photosensitizer.

摘要

光诱导顺铂从铂(IV)前药中释放是一种很有前景的工具,可用于精确时空控制铂基化疗药物的抗增殖活性。将光控化疗(PACT)和光动力疗法(PDT)结合在一个分子中,有可能通过协同效应克服铂基化疗和PDT的关键缺点。在此,我们报道了一种绿光激活的铂(IV)前药GreenPt,其轴向位置带有基于BODIPY的光敏剂,具有极高的光响应和单线态氧生成能力。GreenPt在低剂量绿光照射(高达1 J/cm)下能够释放顺铂。使用DFT建模和ΔG PET估算对GreenPt前药的光还原机制进行研究表明,阴离子自由基的形成以及从BODIPY轴向配体的三重激发态到铂(IV)中心的取代基光诱导电子转移是光诱导顺铂释放的关键步骤。基于绿光激活的BODIPY光敏剂5和8表现出出色的光敏特性,光毒性指数(PI)>1300。GreenPt前药表现出逐渐的细胞内积累和光诱导光毒性,PI>100,从而通过光控释放顺铂和一种有效的基于BODIPY的光敏剂展示了双重作用。

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