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具有高效单线态氧生成的近红外七甲川菁类光动力治疗光敏剂。

Near-Infrared Heptamethine Cyanine Photosensitizers with Efficient Singlet Oxygen Generation for Anticancer Photodynamic Therapy.

机构信息

State Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, Dalian University of Technology, Dalian, 116024, China.

Department of Chemistry, Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction and Institute for Advanced Study, Hong Kong University of Science and Technology, Hong Kong, 999077, China.

出版信息

Angew Chem Int Ed Engl. 2024 Nov 18;63(47):e202411802. doi: 10.1002/anie.202411802. Epub 2024 Sep 17.

DOI:10.1002/anie.202411802
PMID:39081186
Abstract

Near-infrared photosensitizers are valuable tools to improve treatment depth in photodynamic therapy (PDT). However, their low singlet oxygen (O) generation ability, indicated by low O quantum yield, presents a formidable challenge for PDT. To overcome this challenge, the heptamethine cyanine was decorated with biocompatible S (Scy7) and Se (Secy7) atom. We observe that Secy7 exhibits a redshift in the main absorption to ~840 nm and an ultra-efficient O generation capacity. The emergence of a strong intramolecular charge transfer effect between the Se atom and polymethine chain considerably narrows the energy gap (0.51 eV), and the heavy atom effect of Se strengthens spin-orbit coupling (1.44 cm), both of which greatly improved the high triplet state yield (61 %), a state that determines the energy transfer to O. Therefore, Secy7 demonstrated excellent O generation capacity, which is ~24.5-fold that of indocyanine green, ~8.2-fold that of IR780, and ~1.3-fold that of methylene blue under low-power-density 850 nm irradiation (5 mW cm). Secy7 exhibits considerable phototoxicity toward cancer cells buried under 12 mm of tissue. Nanoparticles formed by encapsulating Secy7 within amphiphilic polymers and lecithin, demonstrated promising antitumor and anti-pulmonary metastatic effects, exhibiting remarkable potential for advancing PDT in deep tissues.

摘要

近红外光敏剂是提高光动力疗法(PDT)治疗深度的有价值工具。然而,它们的单线态氧(O)生成能力低,表现为低 O 量子产率,这给 PDT 带来了巨大的挑战。为了克服这一挑战,我们用生物相容性的 S(Scy7)和 Se(Secy7)原子对七甲川花菁进行了修饰。我们观察到 Secy7 在主吸收处表现出红移至840nm,并且具有超高的 O 生成能力。Se 原子和聚甲川链之间强的分子内电荷转移效应大大缩小了能隙(0.51eV),而 Se 的重原子效应增强了自旋轨道耦合(1.44cm),这两者都极大地提高了高三重态产率(61%),这是决定能量向 O 转移的状态。因此,Secy7 表现出优异的 O 生成能力,在低功率密度 850nm 照射(5mW/cm)下,其 O 生成能力是吲哚菁绿的24.5 倍,IR780 的8.2 倍,亚甲蓝的1.3 倍。Secy7 对埋藏在 12mm 组织下的癌细胞具有相当大的光毒性。用两亲聚合物和卵磷脂将 Secy7 封装形成的纳米粒子表现出有前途的抗肿瘤和抗肺转移作用,为推进深部组织 PDT 展现出显著的潜力。

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