Nestoros Eleni, Sharma Amit, Kim Eunji, Kim Jong Seung, Vendrell Marc
Centre for Inflammation Research, Institute for Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
IRR Chemistry Hub, Institute for Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
Nat Rev Chem. 2025 Jan;9(1):46-60. doi: 10.1038/s41570-024-00662-7. Epub 2024 Nov 6.
Photodynamic therapy (PDT) - which combines light, oxygen and photosensitizers (PS) to generate reactive oxygen species - has emerged as an effective approach for targeted ablation of pathogenic cells with reduced risk of inducing resistance. Some organic PS are now being applied for PDT in the clinic or undergoing evaluation in clinical trials. A limitation of the first-generation organic PS was their potential off-target toxicity. This shortcoming prompted the design of constructs that can be activated by the presence of specific biomolecules - from small biomolecules to large enzymes - in the target cells. Here, we review advances in the design and synthesis of activatable organic PS and their contribution to PDT in the past decade. Important areas of research include novel synthetic methodologies to engineer smart PS with tuneable singlet oxygen generation, their integration into larger constructs such as bioconjugates, and finally, representative examples of their translational potential as antimicrobial and anticancer therapies.
光动力疗法(PDT)——它将光、氧和光敏剂(PS)结合以产生活性氧——已成为一种有效的方法,可用于靶向消融致病细胞,且诱导耐药性的风险较低。目前一些有机光敏剂正在临床上用于光动力疗法,或正在临床试验中接受评估。第一代有机光敏剂的一个局限性是它们潜在的脱靶毒性。这一缺点促使人们设计出能够被靶细胞中特定生物分子(从小生物分子到大型酶)激活的构建体。在这里,我们回顾了过去十年中可激活有机光敏剂的设计与合成进展及其对光动力疗法的贡献。重要的研究领域包括用于设计具有可调单线态氧生成能力的智能光敏剂的新型合成方法、将它们整合到更大的构建体(如生物偶联物)中,以及最终作为抗菌和抗癌疗法的转化潜力的代表性实例。