<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yu Y</submitter><funding>Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates</funding><funding>Shenzhen Key Laboratory of Functional Aggregate Materials</funding><funding>National Natural Science Foundation of China</funding><funding>Natural Science Foundation of Guangdong Province</funding><funding>Sichuan Science and Technology Program</funding><pagination>e2302395</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10502865</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(26)</volume><pubmed_abstract>X-ray induced photodynamic therapy (X-PDT) circumvents the poor penetration depth of conventional PDT with minimal radio-resistance generation. However, conventional X-PDT typically requires inorganic scintillators as energy transducers to excite neighboring photosensitizers (PSs) to generate reactive oxygen species (ROS). Herein, a pure organic aggregation-induced emission (AIE) nanoscintillator (TBDCR NPs) that can massively generate both type I and type II ROS under direct X-ray irradiation is reported for hypoxia-tolerant X-PDT. Heteroatoms are introduced to enhance X-ray harvesting and ROS generation ability, and AIE-active TBDCR exhibits aggregation-enhanced ROS especially less oxygen-dependent hydroxyl radical (HO&lt;sup>•-&lt;/sup> , type I) generation ability. TBDCR NPs with a distincti</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Pure Organic AIE Nanoscintillator for X-ray Mediated Type I and Type II Photodynamic Therapy.</pubmed_title><pmcid>PMC10502865</pmcid><funding_grant_id>ZDSYS20211021111400001</funding_grant_id><funding_grant_id>82003242</funding_grant_id><funding_grant_id>22205067</funding_grant_id><funding_grant_id>2019B030301003</funding_grant_id><funding_grant_id>2023YFS0318</funding_grant_id><funding_grant_id>2021A1515011901</funding_grant_id><pubmed_authors>Ni Z</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Xie G</pubmed_authors><pubmed_authors>Zhu ZH</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Feng G</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Tang BZ</pubmed_authors><pubmed_authors>Xiang L</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors><pubmed_authors>Lan J</pubmed_authors><pubmed_authors>Liu W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pure Organic AIE Nanoscintillator for X-ray Mediated Type I and Type II Photodynamic Therapy.</name><description>X-ray induced photodynamic therapy (X-PDT) circumvents the poor penetration depth of conventional PDT with minimal radio-resistance generation. However, conventional X-PDT typically requires inorganic scintillators as energy transducers to excite neighboring photosensitizers (PSs) to generate reactive oxygen species (ROS). Herein, a pure organic aggregation-induced emission (AIE) nanoscintillator (TBDCR NPs) that can massively generate both type I and type II ROS under direct X-ray irradiation is reported for hypoxia-tolerant X-PDT. Heteroatoms are introduced to enhance X-ray harvesting and ROS generation ability, and AIE-active TBDCR exhibits aggregation-enhanced ROS especially less oxygen-dependent hydroxyl radical (HO&lt;sup>•-&lt;/sup> , type I) generation ability. TBDCR NPs with a distincti</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Sep</publication><modification>2025-04-27T03:38:50.507Z</modification><creation>2025-04-06T18:57:15.491Z</creation></dates><accession>S-EPMC10502865</accession><cross_references><pubmed>37424049</pubmed><doi>10.1002/advs.202302395</doi></cross_references></HashMap>