<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Xue L</submitter><pubmed_abstract>Chronic wounds are a major health problem with increasing global prevalence, which endangers the physical and mental health of those affected and is a heavy burden to healthcare providers. &lt;i>Artemisia argyi&lt;/i> extract (AE) has excellent antibacterial and anti-inflammatory properties. In this research, we developed AE loaded composite hydrogel scaffold based on methacrylate gelatin (GelMA)/methacrylate hyaluronic acid (HAMA) and mesoporous silica nanoparticle (MSN) as sustained-release drug carrier vehicles for the treatment of chronic wounds. The presented GelMA/1%HAMA hydrogel possessed stable rheological properties, suitable mechanical properties, appropriate biodegradability, swelling, sustained-release AE capacity. &lt;i>In vitro&lt;/i> antibacterial and cell experiments showed that the GelMA/HAMA/MSN@AE hydrogel had excellent antibacterial activity and biocompatibility and induced macrophages to differentiate into M2 phenotype. &lt;i>In vivo&lt;/i> wound healing of rat full-thickness cutaneous wounds further demonstrated that the prepared GelMA/HAMA/MSN@AE hydrogel could significantly promote chronic wound healing by upregulating the expression of IL-4, TGF-β1, CD31, and α-SMA but downregulating the expression of TNF-α and IFN-γ and promoting M1-M2 macrophages polarization. Altogether, we believe that the GelMA/HAMA/MSN@AE hydrogel will have wide application prospects in healing chronic wounds.</pubmed_abstract><journal>Frontiers in bioengineering and biotechnology</journal><pagination>825339</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8990880</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Composite Hydrogel Containing Mesoporous Silica Nanoparticles Loaded With &lt;i>Artemisia argyi&lt;/i> Extract for Improving Chronic Wound Healing.</pubmed_title><pmcid>PMC8990880</pmcid><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Deng T</pubmed_authors><pubmed_authors>Guo J</pubmed_authors><pubmed_authors>Lu H</pubmed_authors><pubmed_authors>Xue L</pubmed_authors><pubmed_authors>Jiang S</pubmed_authors><pubmed_authors>Deng L</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>Guo R</pubmed_authors><pubmed_authors>Peng L</pubmed_authors><pubmed_authors>Tang F</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Composite Hydrogel Containing Mesoporous Silica Nanoparticles Loaded With &lt;i>Artemisia argyi&lt;/i> Extract for Improving Chronic Wound Healing.</name><description>Chronic wounds are a major health problem with increasing global prevalence, which endangers the physical and mental health of those affected and is a heavy burden to healthcare providers. &lt;i>Artemisia argyi&lt;/i> extract (AE) has excellent antibacterial and anti-inflammatory properties. In this research, we developed AE loaded composite hydrogel scaffold based on methacrylate gelatin (GelMA)/methacrylate hyaluronic acid (HAMA) and mesoporous silica nanoparticle (MSN) as sustained-release drug carrier vehicles for the treatment of chronic wounds. The presented GelMA/1%HAMA hydrogel possessed stable rheological properties, suitable mechanical properties, appropriate biodegradability, swelling, sustained-release AE capacity. &lt;i>In vitro&lt;/i> antibacterial and cell experiments showed that the GelMA/HAMA/MSN@AE hydrogel had excellent antibacterial activity and biocompatibility and induced macrophages to differentiate into M2 phenotype. &lt;i>In vivo&lt;/i> wound healing of rat full-thickness cutaneous wounds further demonstrated that the prepared GelMA/HAMA/MSN@AE hydrogel could significantly promote chronic wound healing by upregulating the expression of IL-4, TGF-β1, CD31, and α-SMA but downregulating the expression of TNF-α and IFN-γ and promoting M1-M2 macrophages polarization. Altogether, we believe that the GelMA/HAMA/MSN@AE hydrogel will have wide application prospects in healing chronic wounds.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T07:34:56.848Z</modification><creation>2025-04-04T07:34:56.848Z</creation></dates><accession>S-EPMC8990880</accession><cross_references><pubmed>35402406</pubmed><doi>10.3389/fbioe.2022.825339</doi></cross_references></HashMap>