<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang S</submitter><funding>Medical Science and Technology Project of Zhejiang Province</funding><funding>Zhejiang Provincial Postdoctoral Science Foundation</funding><funding>Natural Science Foundation of Hubei Province, China</funding><funding>Hubei Provincial Science and Technology Plan Project</funding><funding>Foundation for Innovative Research Groups of Hubei Province</funding><funding>Hubei University of Chinese Medicine 2024 Annual Science and Technology Innovation Project</funding><pagination>93</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12853929</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>The pharmacological activities of traditional herbal medicine-derived carbon dots (THM-CDs) render them highly promising for applications in biomedicine. However, the interactions between THM-CDs and intracellular proteins have yet to be fully elucidated. Herein, inspired by the traditional vinegar-processing of Artemisia argyi (A. argyi), acetic acid-treated Artemisia argyi-derived carbon dots (AA-CDs) demonstrate excellent resistance to iron death via efficient ROS scavenging and Fe&lt;sup>2+&lt;/sup> chelating. Notably, multi-omics analysis uncovers a novel whereby AA-CDs directly target and stabilize heat shock protein A5 (HSPA5), thus preventing the degradation of glutathione peroxidase 4 (GPX4), a pivotal negative regulator of ferroptosis. Emerging evidence indicates that ferroptosis plays</pubmed_abstract><journal>Journal of nanobiotechnology</journal><pubmed_title>Artemisia-derived carbon dots with excellent pharmacological activities and ROS scavenging for osteoarthritis treatment.</pubmed_title><pmcid>PMC12853929</pmcid><funding_grant_id>2026784378</funding_grant_id><funding_grant_id>2025AFD483</funding_grant_id><funding_grant_id>ZY2025J001</funding_grant_id><funding_grant_id>390298</funding_grant_id><funding_grant_id>2024KJCX004</funding_grant_id><funding_grant_id>2025BCB043</funding_grant_id><pubmed_authors>Fan F</pubmed_authors><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Xu K</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Hu X</pubmed_authors><pubmed_authors>Chen G</pubmed_authors><pubmed_authors>Wei K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Artemisia-derived carbon dots with excellent pharmacological activities and ROS scavenging for osteoarthritis treatment.</name><description>The pharmacological activities of traditional herbal medicine-derived carbon dots (THM-CDs) render them highly promising for applications in biomedicine. However, the interactions between THM-CDs and intracellular proteins have yet to be fully elucidated. Herein, inspired by the traditional vinegar-processing of Artemisia argyi (A. argyi), acetic acid-treated Artemisia argyi-derived carbon dots (AA-CDs) demonstrate excellent resistance to iron death via efficient ROS scavenging and Fe&lt;sup>2+&lt;/sup> chelating. Notably, multi-omics analysis uncovers a novel whereby AA-CDs directly target and stabilize heat shock protein A5 (HSPA5), thus preventing the degradation of glutathione peroxidase 4 (GPX4), a pivotal negative regulator of ferroptosis. Emerging evidence indicates that ferroptosis plays</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-13T06:31:06.172Z</modification><creation>2026-06-13T03:12:49.192Z</creation></dates><accession>S-EPMC12853929</accession><cross_references><pubmed>41559762</pubmed><doi>10.1186/s12951-026-04046-5</doi></cross_references></HashMap>