<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Han Z</submitter><funding>Science and Technology Commission of Shanghai Municipality</funding><funding>National Natural Science Foundation of China</funding><pagination>100427</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9526170</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16</volume><pubmed_abstract>Wound healing and angiogenesis remain challenges for both clinical and experimental research worldwide. Periosteum-derived extracellular vesicles (P-sEVs) delivered by hydrogel dressings provide a potential strategy for wound defects to promote fast healing. In this study, we designed a NAGA/GelMA/Laponite/glycerol hydrogel wound dressing that can release P-sEVs to accelerate angiogenesis and wound healing (named P-sEVs@hydrogel) (&lt;i>N&lt;/i>-acryloyl glycinamide, NAGA). The wound dressing showed multiple functions, including efficient angiogenesis, tissue adhesion and a physical barrier. P-sEVs significantly enhanced the proliferation, migration, and tube formation of endothelial cells &lt;i>in vitro&lt;/i>. The results of &lt;i>in vivo&lt;/i> experiments showed that P-sEVs@hydrogel accelerates the healing of a full-thickness defect wound model by stimulating the angiogenic process. The improved cell proliferation, tissue formation, remodeling, and re-epithelialization possibly resulted in the fast healing. This study shows that multifunctional hydrogel dressing combined with bioactive molecules can achieve fast and satisfactory wound healing in full-thickness wound defects and other related wounds.</pubmed_abstract><journal>Materials today. Bio</journal><pubmed_title>Efficient angiogenesis-based wound healing through hydrogel dressing with extracellular vesicles release.</pubmed_title><pmcid>PMC9526170</pmcid><funding_grant_id>82072422</funding_grant_id><funding_grant_id>2020PJD042</funding_grant_id><funding_grant_id>81572178</funding_grant_id><funding_grant_id>52075324</funding_grant_id><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Dong L</pubmed_authors><pubmed_authors>Li A</pubmed_authors><pubmed_authors>Fu L</pubmed_authors><pubmed_authors>Han Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficient angiogenesis-based wound healing through hydrogel dressing with extracellular vesicles release.</name><description>Wound healing and angiogenesis remain challenges for both clinical and experimental research worldwide. Periosteum-derived extracellular vesicles (P-sEVs) delivered by hydrogel dressings provide a potential strategy for wound defects to promote fast healing. In this study, we designed a NAGA/GelMA/Laponite/glycerol hydrogel wound dressing that can release P-sEVs to accelerate angiogenesis and wound healing (named P-sEVs@hydrogel) (&lt;i>N&lt;/i>-acryloyl glycinamide, NAGA). The wound dressing showed multiple functions, including efficient angiogenesis, tissue adhesion and a physical barrier. P-sEVs significantly enhanced the proliferation, migration, and tube formation of endothelial cells &lt;i>in vitro&lt;/i>. The results of &lt;i>in vivo&lt;/i> experiments showed that P-sEVs@hydrogel accelerates the healing of a full-thickness defect wound model by stimulating the angiogenic process. The improved cell proliferation, tissue formation, remodeling, and re-epithelialization possibly resulted in the fast healing. This study shows that multifunctional hydrogel dressing combined with bioactive molecules can achieve fast and satisfactory wound healing in full-thickness wound defects and other related wounds.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-19T11:32:05.812Z</modification><creation>2025-02-19T00:23:41.332Z</creation></dates><accession>S-EPMC9526170</accession><cross_references><pubmed>36193344</pubmed><doi>10.1016/j.mtbio.2022.100427</doi></cross_references></HashMap>