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Chondroitin sulfate sponge scaffold for slow-release Mg 2+ /Cu 2+ in diabetic wound management: Hemostasis, effusion absorption, and healing
The management of diabetic wounds presents significant challenges due to persistent inflammation, microenvironmental disruptions, and impaired angiogenesis. To address these issues, this study developed a multifunctional chondroitin sulfate sponge (CSP@Cu-Mg) with anti-inflammatory properties, hemos...
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Published in: | International journal of biological macromolecules 2024-12, Vol.282 (Pt 6), p.137561 |
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container_issue | Pt 6 |
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container_title | International journal of biological macromolecules |
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creator | Zhu, Fengyi Wen, Qiulan Hu, Yuting Gong, Jun Zhang, Xibing Huang, Chaoyang Zhou, Hai Chen, Lianglong Yu, Li |
description | The management of diabetic wounds presents significant challenges due to persistent inflammation, microenvironmental disruptions, and impaired angiogenesis. To address these issues, this study developed a multifunctional chondroitin sulfate sponge (CSP@Cu-Mg) with anti-inflammatory properties, hemostatic effects, effusion absorption, and enhanced healing promotion. Through ion crosslinking, MgO and CuO were incorporated into the interpenetrating network structure of chondroitin sulfate and acellular dermal matrix, resulting in a sponge with impressive liquid absorption capacity (3450 %) and porosity (83 %). This sponge enabled sustained release of Mg
/Cu
ions, with approximately 40 % cumulative release over 7 days. This release helped reduce inflammation, promote the proliferation and migration of skin repair-related cells, and stimulate angiogenesis. In vivo studies demonstrated that the CSP@Cu-Mg sponge significantly improved diabetic wound healing by modulating inflammation and accelerating collagen deposition, angiogenesis, and re-epithelialization. This extracellular matrix sponge, which synergistically releases Mg
/Cu
, presents a promising strategy for comprehensive diabetic wound management with substantial clinical implications. |
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/Cu
ions, with approximately 40 % cumulative release over 7 days. This release helped reduce inflammation, promote the proliferation and migration of skin repair-related cells, and stimulate angiogenesis. In vivo studies demonstrated that the CSP@Cu-Mg sponge significantly improved diabetic wound healing by modulating inflammation and accelerating collagen deposition, angiogenesis, and re-epithelialization. This extracellular matrix sponge, which synergistically releases Mg
/Cu
, presents a promising strategy for comprehensive diabetic wound management with substantial clinical implications.</description><identifier>EISSN: 1879-0003</identifier><identifier>PMID: 39537068</identifier><language>eng</language><publisher>Netherlands</publisher><subject>Animals ; Chondroitin Sulfates - chemistry ; Chondroitin Sulfates - pharmacology ; Copper - chemistry ; Copper - pharmacology ; Delayed-Action Preparations - pharmacology ; Diabetes Mellitus, Experimental - complications ; Hemostasis - drug effects ; Humans ; Magnesium - chemistry ; Magnesium - pharmacology ; Male ; Mice ; Porosity ; Rats ; Tissue Scaffolds - chemistry ; Wound Healing - drug effects</subject><ispartof>International journal of biological macromolecules, 2024-12, Vol.282 (Pt 6), p.137561</ispartof><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39537068$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Fengyi</creatorcontrib><creatorcontrib>Wen, Qiulan</creatorcontrib><creatorcontrib>Hu, Yuting</creatorcontrib><creatorcontrib>Gong, Jun</creatorcontrib><creatorcontrib>Zhang, Xibing</creatorcontrib><creatorcontrib>Huang, Chaoyang</creatorcontrib><creatorcontrib>Zhou, Hai</creatorcontrib><creatorcontrib>Chen, Lianglong</creatorcontrib><creatorcontrib>Yu, Li</creatorcontrib><title>Chondroitin sulfate sponge scaffold for slow-release Mg 2+ /Cu 2+ in diabetic wound management: Hemostasis, effusion absorption, and healing</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>The management of diabetic wounds presents significant challenges due to persistent inflammation, microenvironmental disruptions, and impaired angiogenesis. To address these issues, this study developed a multifunctional chondroitin sulfate sponge (CSP@Cu-Mg) with anti-inflammatory properties, hemostatic effects, effusion absorption, and enhanced healing promotion. Through ion crosslinking, MgO and CuO were incorporated into the interpenetrating network structure of chondroitin sulfate and acellular dermal matrix, resulting in a sponge with impressive liquid absorption capacity (3450 %) and porosity (83 %). This sponge enabled sustained release of Mg
/Cu
ions, with approximately 40 % cumulative release over 7 days. This release helped reduce inflammation, promote the proliferation and migration of skin repair-related cells, and stimulate angiogenesis. In vivo studies demonstrated that the CSP@Cu-Mg sponge significantly improved diabetic wound healing by modulating inflammation and accelerating collagen deposition, angiogenesis, and re-epithelialization. This extracellular matrix sponge, which synergistically releases Mg
/Cu
, presents a promising strategy for comprehensive diabetic wound management with substantial clinical implications.</description><subject>Animals</subject><subject>Chondroitin Sulfates - chemistry</subject><subject>Chondroitin Sulfates - pharmacology</subject><subject>Copper - chemistry</subject><subject>Copper - pharmacology</subject><subject>Delayed-Action Preparations - pharmacology</subject><subject>Diabetes Mellitus, Experimental - complications</subject><subject>Hemostasis - drug effects</subject><subject>Humans</subject><subject>Magnesium - chemistry</subject><subject>Magnesium - pharmacology</subject><subject>Male</subject><subject>Mice</subject><subject>Porosity</subject><subject>Rats</subject><subject>Tissue Scaffolds - chemistry</subject><subject>Wound Healing - drug effects</subject><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFjsFqAjEURUOhqFV_obx9HTo6qGO3Q4ub7rqXN-ZljCR5Q16C9B_60U2hXXd1zuIeuHdqtm73h6qu62aqHkSuxXbbdTtR0-awbfb1rp2pr-7CQUe2yQaQ7AwmAhk5DAVnNIadBsMRxPGtiuQIheB9gM0TPHf5ByXUFntK9gw3zkGDx4ADeQrpBY7kWRKKlRWQMVksB8BeOI6p6AqwBBdCZ8OwUPcGndDyl3P1-Pb60R2rMfee9GmM1mP8PP3db_4dfANwZVF8</recordid><startdate>202412</startdate><enddate>202412</enddate><creator>Zhu, Fengyi</creator><creator>Wen, Qiulan</creator><creator>Hu, Yuting</creator><creator>Gong, Jun</creator><creator>Zhang, Xibing</creator><creator>Huang, Chaoyang</creator><creator>Zhou, Hai</creator><creator>Chen, Lianglong</creator><creator>Yu, Li</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>202412</creationdate><title>Chondroitin sulfate sponge scaffold for slow-release Mg 2+ /Cu 2+ in diabetic wound management: Hemostasis, effusion absorption, and healing</title><author>Zhu, Fengyi ; Wen, Qiulan ; Hu, Yuting ; Gong, Jun ; Zhang, Xibing ; Huang, Chaoyang ; Zhou, Hai ; Chen, Lianglong ; Yu, Li</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_395370683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Chondroitin Sulfates - chemistry</topic><topic>Chondroitin Sulfates - pharmacology</topic><topic>Copper - chemistry</topic><topic>Copper - pharmacology</topic><topic>Delayed-Action Preparations - pharmacology</topic><topic>Diabetes Mellitus, Experimental - complications</topic><topic>Hemostasis - drug effects</topic><topic>Humans</topic><topic>Magnesium - chemistry</topic><topic>Magnesium - pharmacology</topic><topic>Male</topic><topic>Mice</topic><topic>Porosity</topic><topic>Rats</topic><topic>Tissue Scaffolds - chemistry</topic><topic>Wound Healing - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Fengyi</creatorcontrib><creatorcontrib>Wen, Qiulan</creatorcontrib><creatorcontrib>Hu, Yuting</creatorcontrib><creatorcontrib>Gong, Jun</creatorcontrib><creatorcontrib>Zhang, Xibing</creatorcontrib><creatorcontrib>Huang, Chaoyang</creatorcontrib><creatorcontrib>Zhou, Hai</creatorcontrib><creatorcontrib>Chen, Lianglong</creatorcontrib><creatorcontrib>Yu, Li</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Fengyi</au><au>Wen, Qiulan</au><au>Hu, Yuting</au><au>Gong, Jun</au><au>Zhang, Xibing</au><au>Huang, Chaoyang</au><au>Zhou, Hai</au><au>Chen, Lianglong</au><au>Yu, Li</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chondroitin sulfate sponge scaffold for slow-release Mg 2+ /Cu 2+ in diabetic wound management: Hemostasis, effusion absorption, and healing</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2024-12</date><risdate>2024</risdate><volume>282</volume><issue>Pt 6</issue><spage>137561</spage><pages>137561-</pages><eissn>1879-0003</eissn><abstract>The management of diabetic wounds presents significant challenges due to persistent inflammation, microenvironmental disruptions, and impaired angiogenesis. To address these issues, this study developed a multifunctional chondroitin sulfate sponge (CSP@Cu-Mg) with anti-inflammatory properties, hemostatic effects, effusion absorption, and enhanced healing promotion. Through ion crosslinking, MgO and CuO were incorporated into the interpenetrating network structure of chondroitin sulfate and acellular dermal matrix, resulting in a sponge with impressive liquid absorption capacity (3450 %) and porosity (83 %). This sponge enabled sustained release of Mg
/Cu
ions, with approximately 40 % cumulative release over 7 days. This release helped reduce inflammation, promote the proliferation and migration of skin repair-related cells, and stimulate angiogenesis. In vivo studies demonstrated that the CSP@Cu-Mg sponge significantly improved diabetic wound healing by modulating inflammation and accelerating collagen deposition, angiogenesis, and re-epithelialization. This extracellular matrix sponge, which synergistically releases Mg
/Cu
, presents a promising strategy for comprehensive diabetic wound management with substantial clinical implications.</abstract><cop>Netherlands</cop><pmid>39537068</pmid></addata></record> |
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subjects | Animals Chondroitin Sulfates - chemistry Chondroitin Sulfates - pharmacology Copper - chemistry Copper - pharmacology Delayed-Action Preparations - pharmacology Diabetes Mellitus, Experimental - complications Hemostasis - drug effects Humans Magnesium - chemistry Magnesium - pharmacology Male Mice Porosity Rats Tissue Scaffolds - chemistry Wound Healing - drug effects |
title | Chondroitin sulfate sponge scaffold for slow-release Mg 2+ /Cu 2+ in diabetic wound management: Hemostasis, effusion absorption, and healing |
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