<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lv Q</submitter><funding>Natural Science Foundation of Zhejiang Province</funding><funding>National Natural Science Foundation of China</funding><pagination>e2305895</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11220697</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(25)</volume><pubmed_abstract>Myocardial infarction (MI), a consequence of coronary artery occlusion, triggers the degradation of ferritin, resulting in elevated levels of free iron in the heart and thereby inducing ferroptosis. Targeting myocardial ferroptosis through the chelation of excess iron has therapeutic potential for MI treatment. However, iron chelation in post ischemic injury areas using conventional iron-specific chelators is hindered by ineffective myocardial intracellular chelation, rapid clearance, and high systemic toxicity. A chitosan-desferrioxamine nanosponge (CDNS) is designed by co-crosslinking chitosan and deferoxamine through noncovalent gelation to address these challenges. This architecture facilitates direct iron chelation regardless of deferoxamine (DFO) release due to its sponge-like porous</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Nanosponge for Iron Chelation and Efflux: A Ferroptosis-Inhibiting Approach for Myocardial Infarction Therapy.</pubmed_title><pmcid>PMC11220697</pmcid><funding_grant_id>22105169</funding_grant_id><funding_grant_id>LQ21B010002</funding_grant_id><funding_grant_id>82200375</funding_grant_id><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Ma B</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Huang H</pubmed_authors><pubmed_authors>Fu G</pubmed_authors><pubmed_authors>Xiao Y</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Lv Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nanosponge for Iron Chelation and Efflux: A Ferroptosis-Inhibiting Approach for Myocardial Infarction Therapy.</name><description>Myocardial infarction (MI), a consequence of coronary artery occlusion, triggers the degradation of ferritin, resulting in elevated levels of free iron in the heart and thereby inducing ferroptosis. Targeting myocardial ferroptosis through the chelation of excess iron has therapeutic potential for MI treatment. However, iron chelation in post ischemic injury areas using conventional iron-specific chelators is hindered by ineffective myocardial intracellular chelation, rapid clearance, and high systemic toxicity. A chitosan-desferrioxamine nanosponge (CDNS) is designed by co-crosslinking chitosan and deferoxamine through noncovalent gelation to address these challenges. This architecture facilitates direct iron chelation regardless of deferoxamine (DFO) release due to its sponge-like porous</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-04T19:23:46.404Z</modification><creation>2025-04-04T19:23:46.404Z</creation></dates><accession>S-EPMC11220697</accession><cross_references><pubmed>38671590</pubmed><doi>10.1002/advs.202305895</doi></cross_references></HashMap>