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不对称苯并噻吩并 BODIPYs 作为高效近红外重原子自由光敏剂。

Unsymmetrical Benzothieno-Fused BODIPYs as Efficient NIR Heavy-Atom-Free Photosensitizers.

机构信息

College of Chemistry and Chemical Engineering, Yantai University, Yantai 264005, China.

The Key Laboratory of Functional Molecular Solids, Ministry of Education, School of Chemistry and Materials Science, Anhui Normal University, Wuhu 241002, China.

出版信息

J Org Chem. 2024 Apr 5;89(7):4826-4839. doi: 10.1021/acs.joc.4c00034. Epub 2024 Mar 12.

Abstract

Heavy-atom-free photosensitizers are potentially suitable for use in photodynamic therapy (PDT). In this contribution, a new family of unsymmetrical benzothieno-fused BODIPYs with reactive oxygen efficiency up to 50% in air-saturated toluene was reported. Their efficient intersystem crossing (ISC) resulted in the generation of both O and O under irradiation. More importantly, the PDT efficacy of a respective 4-methoxystyryl-modified benzothieno-fused BODIPY in living cells exhibited an extremely high phototoxicity with an ultralow IC value of 2.78 nM. The results revealed that the incorporation of an electron-donating group at the α-position of the unsymmetrical benzothieno-fused BODIPY platform might be an effective approach for developing long-wavelength absorbing heavy-atom-free photosensitizers for precision cancer therapy.

摘要

无重原子敏化剂在光动力疗法(PDT)中具有潜在的应用价值。本研究报道了一类新型的非对称苯并噻吩并 BODIPY,其在空气饱和的甲苯中具有高达 50%的活性氧效率。它们具有高效的系间跨越(ISC),在光照下产生 O 和 O。更重要的是,相应的 4-甲氧基苯乙烯基修饰的苯并噻吩并 BODIPY 在活细胞中的 PDT 疗效表现出极高的光毒性,IC 值低至 2.78 nM。结果表明,在非对称苯并噻吩并 BODIPY 平台的α位引入供电子基团可能是开发用于精准癌症治疗的长波长吸收无重原子敏化剂的有效方法。

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