Qiao Hu, Jianjun Du, Syed Ali Abbas Abedi, Xiaogang Liu, Saran Long, Wen Sun, Jiangli Fan, Xiaojun Peng
{"title":"Unveiling the Power of Dark State Photocages: An Efficient Pathway to Triplet State Under Near-Infrared Light Irradiation.","authors":"Qiao Hu, Jianjun Du, Syed Ali Abbas Abedi, Xiaogang Liu, Saran Long, Wen Sun, Jiangli Fan, Xiaojun Peng","doi":"10.1002/anie.202504670","DOIUrl":null,"url":null,"abstract":"<p><p>The photocage platform provides a synergistic approach to photodynamic therapy (PDT) and chemotherapy. Before light activation, both pro-photosensitizers and pro-drugs remain inert, ensuring safety. Upon near-infrared (NIR) light irradiation, they undergo photoactivation and controlled release in deep tissues. However, the low photolysis efficiency of conventional singlet-state photocages limits their in vivo applications, necessitating an exploration of how excited-state dynamics influence photolysis. In this study, we introduce the concept of a \"dark state photocage\" and establish a photocage platform responsive to NIR light by incorporating phenoxazine or phenothiazine groups. Mechanistic investigations reveal that the dark state enhances triplet-state formation and facilitates intersystem crossing, thereby promoting photolysis. These photocages achieve functional molecule release under low-power NIR light (15 mW cm⁻<sup>2</sup>), with an efficiency of up to 90%. This advancement enables a sharp transition from an \"OFF\" to an \"ON\" tumor imaging signal and significantly enhances the therapeutic efficacy against triple-negative breast cancer under NIR light irradiation, effectively integrating PDT and chemotherapy.</p>","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202504670"},"PeriodicalIF":16.9000,"publicationDate":"2025-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie (International ed. in English)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/anie.202504670","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/14 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The photocage platform provides a synergistic approach to photodynamic therapy (PDT) and chemotherapy. Before light activation, both pro-photosensitizers and pro-drugs remain inert, ensuring safety. Upon near-infrared (NIR) light irradiation, they undergo photoactivation and controlled release in deep tissues. However, the low photolysis efficiency of conventional singlet-state photocages limits their in vivo applications, necessitating an exploration of how excited-state dynamics influence photolysis. In this study, we introduce the concept of a "dark state photocage" and establish a photocage platform responsive to NIR light by incorporating phenoxazine or phenothiazine groups. Mechanistic investigations reveal that the dark state enhances triplet-state formation and facilitates intersystem crossing, thereby promoting photolysis. These photocages achieve functional molecule release under low-power NIR light (15 mW cm⁻2), with an efficiency of up to 90%. This advancement enables a sharp transition from an "OFF" to an "ON" tumor imaging signal and significantly enhances the therapeutic efficacy against triple-negative breast cancer under NIR light irradiation, effectively integrating PDT and chemotherapy.