{"title":"Self-Powered α Radionuclide Nanomedicine: Mitochondria-Targeted Multimodal Energy Recycling for Amplified Radioimmunotherapy.","authors":"Xian Li,Chaochao Wang,Yelin Wu,Jiajia Zhang,Han Zhang,Shanshan Qin,Linglin Tang,Fei Yu","doi":"10.1002/adma.202504612","DOIUrl":null,"url":null,"abstract":"Internal Radionuclide Therapy (IRT) faces significant challenges, particularly the limited controlled penetration depth of conventional β rays and the inefficient targeted delivery of α-emitters. In this study, a mitochondria-targeted, self-powered α radionuclide nanomedicine, and pioneer a groundbreaking \"suborganelle precise radiodynamic immunotherapy\" paradigm that synergistically integrates physical irradiation, catalytic chemistry, and immunomodulation to overcome the historical limitations of IRT is developed. The innovation establishes a \"radionuclide energy internal cycling\" strategy through 223RaCl2 (the first FDA-approved α-emitter), unlocking three synergistic therapies from one radionuclide: precise ionizing radiation, self-powered catalysis, and immunogenic reprogramming. This paradigm uniquely exploits the full decay spectrum (α particles, β electrons, γ photons) to synchronize physical, chemical, and biological anti-tumor mechanisms without requiring external energy inputs, offering a transformative solution to overcome the physical-biological barriers of IRT and bridge localized eradication with systemic immune regulation.","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":"104 1","pages":"e2504612"},"PeriodicalIF":27.4000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adma.202504612","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Internal Radionuclide Therapy (IRT) faces significant challenges, particularly the limited controlled penetration depth of conventional β rays and the inefficient targeted delivery of α-emitters. In this study, a mitochondria-targeted, self-powered α radionuclide nanomedicine, and pioneer a groundbreaking "suborganelle precise radiodynamic immunotherapy" paradigm that synergistically integrates physical irradiation, catalytic chemistry, and immunomodulation to overcome the historical limitations of IRT is developed. The innovation establishes a "radionuclide energy internal cycling" strategy through 223RaCl2 (the first FDA-approved α-emitter), unlocking three synergistic therapies from one radionuclide: precise ionizing radiation, self-powered catalysis, and immunogenic reprogramming. This paradigm uniquely exploits the full decay spectrum (α particles, β electrons, γ photons) to synchronize physical, chemical, and biological anti-tumor mechanisms without requiring external energy inputs, offering a transformative solution to overcome the physical-biological barriers of IRT and bridge localized eradication with systemic immune regulation.
期刊介绍:
Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.