Chemistry Department, University of Coimbra, Coimbra, Portugal.
Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
Photochem Photobiol. 2020 May;96(3):692-698. doi: 10.1111/php.13256. Epub 2020 Apr 28.
Predicting the extent of necrosis in photodynamic therapy (PDT) is critical to ensure that the whole tumor is treated but vital structures, such as major blood vessels in the vicinity of the tumor, are spared. The models developed for clinical planning rely on empirical parameters that change with the nature of the photosensitizer and the target tissue. This work presents an in vivo study of the necrosis in the livers of rats due to PDT with a bacteriochlorin photosensitizer named redaporfin using both frontal illumination and interstitial illumination. Various doses of light at 750 nm were delivered 15 min postintravenous administration of redaporfin. Sharp boundaries between necrotic and healthy tissues were found. Frontal illumination allowed for the determination of the photodynamic threshold dose-1.5 × 10 photons cm -which means that the regions of the tissues exposed to more than 11 mm of ROS evolved to necrosis. Interstitial illumination produced a necrotic radius of 0.7 cm for a light dose of 100 J cm and a redaporfin dose of 0.75 mg kg . The experimental data obtained can be used to inform and improve clinical planning with frontal and interstitial illumination protocols.
预测光动力疗法 (PDT) 中的坏死范围对于确保整个肿瘤得到治疗至关重要,但同时也要保护重要结构,如肿瘤附近的主要血管。用于临床规划的模型依赖于随光敏剂和靶组织性质而变化的经验参数。这项工作研究了使用名为 redaporfin 的细菌叶绿素光敏剂进行 PDT 后大鼠肝脏的坏死情况,分别采用了前向照明和间质照明。在静脉注射 redaporfin 15 分钟后,以 750nm 的各种剂量的光进行照射。在坏死和健康组织之间发现了明显的边界。前向照明允许确定光动力阈值剂量-1.5×10 光子 cm -,这意味着暴露于超过 11mm 活性氧的组织区域会发展为坏死。对于 100J/cm 的光剂量和 0.75mg/kg 的 redaporfin 剂量,间质照明产生了 0.7cm 的坏死半径。可以使用获得的实验数据来告知和改进前向和间质照明方案的临床规划。