{"title":"γ-放射性核素技术- 99m激活的长效化学动力疗法和免疫原性近距离放疗增强抗肿瘤免疫。","authors":"Naihan Huang, Wen Li, Lin Liu, Weibing Miao","doi":"10.1002/adhm.71795","DOIUrl":null,"url":null,"abstract":"<p><p>Chemodynamic therapy (CDT) and brachytherapy face critical challenges, particularly the limited efficiency of Fenton reaction and the insufficient antitumor immunogenicity of brachytherapy. In this study, we employ the metal-organic framework nanocomposite Hf-TCPP@Fe-<sup>99m</sup>Tc (where TCPP = tetrakis(4-carboxyphenyl) porphyrin and <sup>99m</sup>Tc = technetium-99m) for synergistic long-lasting CDT and immunogenic brachytherapy. Benefiting from the robust interaction between <sup>99m</sup>Tc-emitted γ-rays and the high-Z element Hf, the secondary electrons generated during brachytherapy not only damage tumor cells but also establish an electron-rich microenvironment that drives the continuous reduction of Fe<sup>3+</sup> to Fe<sup>2+</sup>, thereby sustaining a highly efficient Fenton reaction. With the generation of hydroxyl radical persisting for over 12 h, this synergistic effect reduced cell viability by an additional 28.6% beyond projections, thereby inducing effective immunogenic cell death, activating a systemic antitumor immune response, and inhibiting both primary and metastatic triple-negative breast cancer. Through rational design, this work demonstrates that clinically prevalent nontherapeutic γ-radionuclide can activate long-lasting CDT and immunogenic brachytherapy to enhance antitumor immunogenicity.</p>","PeriodicalId":113,"journal":{"name":"Advanced Healthcare Materials","volume":" ","pages":""},"PeriodicalIF":11.0000,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"γ-Radionuclide Technetium-99M Activated Long-Lasting Chemodynamic Therapy and Immunogenic Brachytherapy for Enhanced Antitumor Immunity.\",\"authors\":\"Naihan Huang, Wen Li, Lin Liu, Weibing Miao\",\"doi\":\"10.1002/adhm.71795\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Chemodynamic therapy (CDT) and brachytherapy face critical challenges, particularly the limited efficiency of Fenton reaction and the insufficient antitumor immunogenicity of brachytherapy. In this study, we employ the metal-organic framework nanocomposite Hf-TCPP@Fe-<sup>99m</sup>Tc (where TCPP = tetrakis(4-carboxyphenyl) porphyrin and <sup>99m</sup>Tc = technetium-99m) for synergistic long-lasting CDT and immunogenic brachytherapy. Benefiting from the robust interaction between <sup>99m</sup>Tc-emitted γ-rays and the high-Z element Hf, the secondary electrons generated during brachytherapy not only damage tumor cells but also establish an electron-rich microenvironment that drives the continuous reduction of Fe<sup>3+</sup> to Fe<sup>2+</sup>, thereby sustaining a highly efficient Fenton reaction. With the generation of hydroxyl radical persisting for over 12 h, this synergistic effect reduced cell viability by an additional 28.6% beyond projections, thereby inducing effective immunogenic cell death, activating a systemic antitumor immune response, and inhibiting both primary and metastatic triple-negative breast cancer. Through rational design, this work demonstrates that clinically prevalent nontherapeutic γ-radionuclide can activate long-lasting CDT and immunogenic brachytherapy to enhance antitumor immunogenicity.</p>\",\"PeriodicalId\":113,\"journal\":{\"name\":\"Advanced Healthcare Materials\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":11.0000,\"publicationDate\":\"2026-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Healthcare Materials\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1002/adhm.71795\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2026/10/9 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, BIOMEDICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Healthcare Materials","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/adhm.71795","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/10/9 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
γ-Radionuclide Technetium-99M Activated Long-Lasting Chemodynamic Therapy and Immunogenic Brachytherapy for Enhanced Antitumor Immunity.
Chemodynamic therapy (CDT) and brachytherapy face critical challenges, particularly the limited efficiency of Fenton reaction and the insufficient antitumor immunogenicity of brachytherapy. In this study, we employ the metal-organic framework nanocomposite Hf-TCPP@Fe-99mTc (where TCPP = tetrakis(4-carboxyphenyl) porphyrin and 99mTc = technetium-99m) for synergistic long-lasting CDT and immunogenic brachytherapy. Benefiting from the robust interaction between 99mTc-emitted γ-rays and the high-Z element Hf, the secondary electrons generated during brachytherapy not only damage tumor cells but also establish an electron-rich microenvironment that drives the continuous reduction of Fe3+ to Fe2+, thereby sustaining a highly efficient Fenton reaction. With the generation of hydroxyl radical persisting for over 12 h, this synergistic effect reduced cell viability by an additional 28.6% beyond projections, thereby inducing effective immunogenic cell death, activating a systemic antitumor immune response, and inhibiting both primary and metastatic triple-negative breast cancer. Through rational design, this work demonstrates that clinically prevalent nontherapeutic γ-radionuclide can activate long-lasting CDT and immunogenic brachytherapy to enhance antitumor immunogenicity.
期刊介绍:
Advanced Healthcare Materials, a distinguished member of the esteemed Advanced portfolio, has been dedicated to disseminating cutting-edge research on materials, devices, and technologies for enhancing human well-being for over ten years. As a comprehensive journal, it encompasses a wide range of disciplines such as biomaterials, biointerfaces, nanomedicine and nanotechnology, tissue engineering, and regenerative medicine.