Huihui Liu, Jie Guo, Wangjing Yin, Hehua Xiong, Ling Chen, Yiling Ruan, Kai Feng, Dan Su, Yi Liu, Xiaolian Sun
{"title":"双锁纳米光敏剂利用切伦科夫辐射治疗深部肿瘤","authors":"Huihui Liu, Jie Guo, Wangjing Yin, Hehua Xiong, Ling Chen, Yiling Ruan, Kai Feng, Dan Su, Yi Liu, Xiaolian Sun","doi":"10.1021/acs.jmedchem.5c02387","DOIUrl":null,"url":null,"abstract":"Photodynamic therapy (PDT) faces significant challenges in treating deep tumors due to the limited light penetration depth. Cerenkov radiation-induced PDT (CR-PDT) offers a potential solution by harnessing luminescence derived from radionuclides. However, the simultaneous delivery of radionuclides and photosensitizers in conventional CR-PDT systems leads to unnecessary phototoxicity of healthy tissues. Here, we present a tumor microenvironment (TME)-activated, dual-locked nanophotosensitizer (<sup>89</sup>Zr-PHZ-BrCyE) that integrates <sup>89</sup>Zr-labeled pH-responsive polymeric micelle and a carboxylesterase (CrES)-activated photosensitizer prodrug for precise deep tumor therapy. The dual-responsive CR-PDT system demonstrated highly selective cytotoxicity toward hepatocellular carcinoma (HepG2) cells, with minimal impact on normal liver cells (L02). Upon intravenous injection, <sup>89</sup>Zr-PHZ-BrCyE exhibited robust tumor inhibition and excellent biosafety in both subcutaneous and orthotopic H22 tumor models. This approach holds great promise for improving the therapeutic outcomes of CR-PDT in deep-seated tumors while ensuring good biosafety, paving the way for future potential clinical applications in the future.","PeriodicalId":46,"journal":{"name":"Journal of Medicinal Chemistry","volume":"89 1","pages":""},"PeriodicalIF":6.8000,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dual-Locked Nanophotosensitizer Harnessing Cerenkov Radiation for Deep Tumor Therapy\",\"authors\":\"Huihui Liu, Jie Guo, Wangjing Yin, Hehua Xiong, Ling Chen, Yiling Ruan, Kai Feng, Dan Su, Yi Liu, Xiaolian Sun\",\"doi\":\"10.1021/acs.jmedchem.5c02387\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Photodynamic therapy (PDT) faces significant challenges in treating deep tumors due to the limited light penetration depth. Cerenkov radiation-induced PDT (CR-PDT) offers a potential solution by harnessing luminescence derived from radionuclides. However, the simultaneous delivery of radionuclides and photosensitizers in conventional CR-PDT systems leads to unnecessary phototoxicity of healthy tissues. Here, we present a tumor microenvironment (TME)-activated, dual-locked nanophotosensitizer (<sup>89</sup>Zr-PHZ-BrCyE) that integrates <sup>89</sup>Zr-labeled pH-responsive polymeric micelle and a carboxylesterase (CrES)-activated photosensitizer prodrug for precise deep tumor therapy. The dual-responsive CR-PDT system demonstrated highly selective cytotoxicity toward hepatocellular carcinoma (HepG2) cells, with minimal impact on normal liver cells (L02). Upon intravenous injection, <sup>89</sup>Zr-PHZ-BrCyE exhibited robust tumor inhibition and excellent biosafety in both subcutaneous and orthotopic H22 tumor models. This approach holds great promise for improving the therapeutic outcomes of CR-PDT in deep-seated tumors while ensuring good biosafety, paving the way for future potential clinical applications in the future.\",\"PeriodicalId\":46,\"journal\":{\"name\":\"Journal of Medicinal Chemistry\",\"volume\":\"89 1\",\"pages\":\"\"},\"PeriodicalIF\":6.8000,\"publicationDate\":\"2025-10-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Medicinal Chemistry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.jmedchem.5c02387\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medicinal Chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1021/acs.jmedchem.5c02387","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Dual-Locked Nanophotosensitizer Harnessing Cerenkov Radiation for Deep Tumor Therapy
Photodynamic therapy (PDT) faces significant challenges in treating deep tumors due to the limited light penetration depth. Cerenkov radiation-induced PDT (CR-PDT) offers a potential solution by harnessing luminescence derived from radionuclides. However, the simultaneous delivery of radionuclides and photosensitizers in conventional CR-PDT systems leads to unnecessary phototoxicity of healthy tissues. Here, we present a tumor microenvironment (TME)-activated, dual-locked nanophotosensitizer (89Zr-PHZ-BrCyE) that integrates 89Zr-labeled pH-responsive polymeric micelle and a carboxylesterase (CrES)-activated photosensitizer prodrug for precise deep tumor therapy. The dual-responsive CR-PDT system demonstrated highly selective cytotoxicity toward hepatocellular carcinoma (HepG2) cells, with minimal impact on normal liver cells (L02). Upon intravenous injection, 89Zr-PHZ-BrCyE exhibited robust tumor inhibition and excellent biosafety in both subcutaneous and orthotopic H22 tumor models. This approach holds great promise for improving the therapeutic outcomes of CR-PDT in deep-seated tumors while ensuring good biosafety, paving the way for future potential clinical applications in the future.
期刊介绍:
The Journal of Medicinal Chemistry is a prestigious biweekly peer-reviewed publication that focuses on the multifaceted field of medicinal chemistry. Since its inception in 1959 as the Journal of Medicinal and Pharmaceutical Chemistry, it has evolved to become a cornerstone in the dissemination of research findings related to the design, synthesis, and development of therapeutic agents.
The Journal of Medicinal Chemistry is recognized for its significant impact in the scientific community, as evidenced by its 2022 impact factor of 7.3. This metric reflects the journal's influence and the importance of its content in shaping the future of drug discovery and development. The journal serves as a vital resource for chemists, pharmacologists, and other researchers interested in the molecular mechanisms of drug action and the optimization of therapeutic compounds.