<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jin N</submitter><funding>Research and Cultivation Program of Stomatological Hospital of Southern Medical University</funding><funding>National Natural Science Foundation of China</funding><funding>China Postdoctoral Science Foundation</funding><funding>2018 Scientist Partners of China Medical University (CMU) and Shenyang Branch of Chinese Academy of Sciences</funding><funding>Key Research &amp;amp; Development Project of Liaoning Province</funding><pagination>e2400526</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11468540</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(16)</volume><pubmed_abstract>The management of diabetic wounds (DWs) continues to pose a significant challenge in the field of medicine. DWs are primarily prevented from healing due to damage to macrophage efferocytosis and fibroblast dysfunction. Consequently, a treatment strategy that involves both immunoregulation and the promotion of extracellular matrix (ECM) formation holds promise for healing DWs. Nevertheless, existing treatment methods necessitate complex interventions and are associated with increased costs, for example, the use of cytokines and cell therapy, both of which have limited effectiveness. In this study, a new type of ruthenium (IV) oxide nanoparticles (RNPs)-laden hybrid hydrogel dressing with a double network of Pluronic F127 and F68 has been developed. Notably, the hybrid hydrogel demonstrates </pubmed_abstract><journal>Advanced healthcare materials</journal><pubmed_title>Promoting Diabetic Wound Healing through a Hydrogel-Based Cascade Regulation Strategy of Fibroblast-Macrophage.</pubmed_title><pmcid>PMC11468540</pmcid><funding_grant_id>82301026</funding_grant_id><funding_grant_id>81571832</funding_grant_id><funding_grant_id>2018225082</funding_grant_id><funding_grant_id>2023M731547</funding_grant_id><funding_grant_id>HZHB2018013</funding_grant_id><funding_grant_id>PY2022005</funding_grant_id><pubmed_authors>Jin N</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Tang X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Promoting Diabetic Wound Healing through a Hydrogel-Based Cascade Regulation Strategy of Fibroblast-Macrophage.</name><description>The management of diabetic wounds (DWs) continues to pose a significant challenge in the field of medicine. DWs are primarily prevented from healing due to damage to macrophage efferocytosis and fibroblast dysfunction. Consequently, a treatment strategy that involves both immunoregulation and the promotion of extracellular matrix (ECM) formation holds promise for healing DWs. Nevertheless, existing treatment methods necessitate complex interventions and are associated with increased costs, for example, the use of cytokines and cell therapy, both of which have limited effectiveness. In this study, a new type of ruthenium (IV) oxide nanoparticles (RNPs)-laden hybrid hydrogel dressing with a double network of Pluronic F127 and F68 has been developed. Notably, the hybrid hydrogel demonstrates </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2025-04-22T10:48:19.299Z</modification><creation>2025-04-05T23:46:09.621Z</creation></dates><accession>S-EPMC11468540</accession><cross_references><pubmed>38469978</pubmed><doi>10.1002/adhm.202400526</doi></cross_references></HashMap>