Department of Pharmaceutical Science and Technology, College of Biological Science and Medical Engineering, Donghua University, Shanghai 201620, China.
Department of Pharmacy, Huadong Hospital, Fudan University, Shanghai 200040, China; Shanghai Xianhui Pharmaceutical Co., Ltd., Shanghai 201620, China.
Bioorg Chem. 2024 Oct;151:107710. doi: 10.1016/j.bioorg.2024.107710. Epub 2024 Aug 14.
Photodynamic therapy (PDT) is a well-established treatment modality, typically conducted with single-wavelength irradiation, which may not always be optimal for varying tumor locations and sizes. To address this, photosensitizers with absorption wavelengths ranging from 550 to 760 nm are being explored. Herein, a series of 5,15-diaryltetrabenzoporphyrins (ArTBPs) were synthesized. All compounds displayed obvious absorption at 550-700 nm (especially at ∼668 nm), intense fluorescence, efficient generation of singlet oxygen and good photodynamic antitumor effects. Notably, compound I (5,15-bis[(4-carboxymethoxy)phenyl]tetrabenzoporphyrin) showed excellent cytotoxicity against Eca-109 cell line upon red light irradiation, with an IC value of 0.45 μM, and phototherapeutic index of 25.8. Flow cytometry revealed that I could induce distinct cell apoptosis. In vivo studies revealed that compound I selectively accumulated at tumor site and exhibited outstanding PDT effect with antitumor activity under single-time administration and light irradiation, and revealed more efficiency than the clinical photosensitizer Verteporfin. These findings underscore the considerable promise of I as a robust theranostic agent, offering capabilities in real-time fluorescence imaging and serving as a potent photosensitizer for personalized and precise photodynamic therapy of tumors.
光动力疗法(PDT)是一种成熟的治疗方式,通常采用单波长照射,但对于不同的肿瘤位置和大小,这种方法并不总是最佳选择。为了解决这个问题,人们正在探索吸收波长在 550 到 760nm 之间的光敏剂。本文合成了一系列 5,15-二芳基四苯并卟啉(ArTBPs)。所有化合物在 550-700nm 处均显示明显吸收(特别是在约 668nm 处),具有强荧光、高效生成单线态氧和良好的光动力抗肿瘤效果。值得注意的是,化合物 I(5,15-双[(4-羧甲氧苯基)]四苯并卟啉)在红光照射下对 Eca-109 细胞系表现出优异的细胞毒性,IC 值为 0.45μM,光治疗指数为 25.8。流式细胞术显示 I 可以诱导明显的细胞凋亡。体内研究表明,化合物 I 选择性地在肿瘤部位积聚,并在单次给药和光照下表现出出色的 PDT 效果,其抗肿瘤活性优于临床用光敏剂 Verteporfin。这些发现表明 I 作为一种强大的治疗诊断试剂具有很大的应用潜力,能够实时荧光成像,并作为一种有效的光敏剂用于肿瘤的个性化和精确光动力治疗。