Remodeling Microenvironment for Implant‐Associated Osteomyelitis by Dual Metal Peroxide
Implant‐associated osteomyelitis (IAOM) is characterized by bone infection and destruction; current therapy of antibiotic treatment and surgical debridement often results in drug resistance and bone defect. It is challenging to develop an antibiotic‐free bactericidal and osteogenic‐enhanced strategy...
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description | Implant‐associated osteomyelitis (IAOM) is characterized by bone infection and destruction; current therapy of antibiotic treatment and surgical debridement often results in drug resistance and bone defect. It is challenging to develop an antibiotic‐free bactericidal and osteogenic‐enhanced strategy for IAOM. Herein, an IAOM‐tailored antibacterial and osteoinductive composite of copper (Cu)–strontium (Sr) peroxide nanoparticles (CSp NPs), encapsulated in polyethylene glycol diacrylate (PEGDA) (CSp@PEGDA), is designed. The dual functional CSp NPs display hydrogen peroxide (H2O2) self‐supplying and Fenton catalytic Cu2+ ions’ release, generating plenty of hydroxyl radical (•OH) in a pH‐responsive manner for bacterial killing, while the released Sr2+ promotes the in vitro osteogenicity regarding cell proliferation, alkaline phosphatase activity, extracellular matrix calcification, and osteo‐associated genes expression. The integration of Cu2+ and Sr2+ in CSp NPs together with the coated PEGDA hydrogel ensures the stable and sustainable ion release during short‐ and long‐term periods. Benefitted from the injectablity and photo‐crosslink ability, CSp@PEGDA is able to thoroughly fill the infectious site and gelate in situ for bacterial elimination and bone regeneration, which is verified through in vivo evaluation using a clinical‐simulating IAOM mouse model. These favorable abilities of CSp@PEGDA precisely meet the multiple therapeutic needs and pave a promising way for implant‐associated osteomyelitis treatment.
Copper–strontium peroxide nanoparticle‐loaded polyethylene glycol diacrylate (PEGDA) composites tailored for implant‐associated osteomyelitis (IAOM) are constructed with outstanding antibacterial and osteoinductive capabilities in this study, which exhibit effective catalytic power for Fenton‐like reaction and controllable ion release behavior. This research offers a novel and promising treatment strategy for IAOM. |
doi_str_mv | 10.1002/adhm.202303529 |
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Copper–strontium peroxide nanoparticle‐loaded polyethylene glycol diacrylate (PEGDA) composites tailored for implant‐associated osteomyelitis (IAOM) are constructed with outstanding antibacterial and osteoinductive capabilities in this study, which exhibit effective catalytic power for Fenton‐like reaction and controllable ion release behavior. This research offers a novel and promising treatment strategy for IAOM.</description><identifier>ISSN: 2192-2640</identifier><identifier>ISSN: 2192-2659</identifier><identifier>EISSN: 2192-2659</identifier><identifier>DOI: 10.1002/adhm.202303529</identifier><identifier>PMID: 38430010</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Alkaline phosphatase ; antibacteria ; Antibiotics ; Bone growth ; Bone implants ; Calcification ; Cell proliferation ; chemodynamic therapy ; Copper ; Drug resistance ; Extracellular matrix ; Gene expression ; Hydrogen peroxide ; Hydroxyl radicals ; implant‐associated osteomyelitis ; metal peroxide ; Microenvironments ; Nanoparticles ; Osteogenesis ; Osteomyelitis ; Polyethylene glycol ; Regeneration ; Regeneration (physiology) ; Strontium</subject><ispartof>Advanced healthcare materials, 2024-06, Vol.13 (16), p.e2303529-n/a</ispartof><rights>2024 Wiley‐VCH GmbH</rights><rights>2024 Wiley-VCH GmbH.</rights><rights>2024 Wiley‐VCH GmbH.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3739-bd61faa391cad7c90b0634c9ccbc0a48580ecf3e1cd95dacbd4085bb9a837c8a3</citedby><cites>FETCH-LOGICAL-c3739-bd61faa391cad7c90b0634c9ccbc0a48580ecf3e1cd95dacbd4085bb9a837c8a3</cites><orcidid>0000-0002-6914-0605</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fadhm.202303529$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fadhm.202303529$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38430010$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guan, Xin</creatorcontrib><creatorcontrib>Wu, Siyuan</creatorcontrib><creatorcontrib>Ouyang, Sixue</creatorcontrib><creatorcontrib>Ren, Shuchen</creatorcontrib><creatorcontrib>Cui, Naiqian</creatorcontrib><creatorcontrib>Wu, Xiaohu</creatorcontrib><creatorcontrib>Xiang, Dayong</creatorcontrib><creatorcontrib>Chen, Wenting</creatorcontrib><creatorcontrib>Yu, Bin</creatorcontrib><creatorcontrib>Zhao, Peng</creatorcontrib><creatorcontrib>Wang, Bowei</creatorcontrib><title>Remodeling Microenvironment for Implant‐Associated Osteomyelitis by Dual Metal Peroxide</title><title>Advanced healthcare materials</title><addtitle>Adv Healthc Mater</addtitle><description>Implant‐associated osteomyelitis (IAOM) is characterized by bone infection and destruction; current therapy of antibiotic treatment and surgical debridement often results in drug resistance and bone defect. It is challenging to develop an antibiotic‐free bactericidal and osteogenic‐enhanced strategy for IAOM. Herein, an IAOM‐tailored antibacterial and osteoinductive composite of copper (Cu)–strontium (Sr) peroxide nanoparticles (CSp NPs), encapsulated in polyethylene glycol diacrylate (PEGDA) (CSp@PEGDA), is designed. The dual functional CSp NPs display hydrogen peroxide (H2O2) self‐supplying and Fenton catalytic Cu2+ ions’ release, generating plenty of hydroxyl radical (•OH) in a pH‐responsive manner for bacterial killing, while the released Sr2+ promotes the in vitro osteogenicity regarding cell proliferation, alkaline phosphatase activity, extracellular matrix calcification, and osteo‐associated genes expression. The integration of Cu2+ and Sr2+ in CSp NPs together with the coated PEGDA hydrogel ensures the stable and sustainable ion release during short‐ and long‐term periods. Benefitted from the injectablity and photo‐crosslink ability, CSp@PEGDA is able to thoroughly fill the infectious site and gelate in situ for bacterial elimination and bone regeneration, which is verified through in vivo evaluation using a clinical‐simulating IAOM mouse model. These favorable abilities of CSp@PEGDA precisely meet the multiple therapeutic needs and pave a promising way for implant‐associated osteomyelitis treatment.
Copper–strontium peroxide nanoparticle‐loaded polyethylene glycol diacrylate (PEGDA) composites tailored for implant‐associated osteomyelitis (IAOM) are constructed with outstanding antibacterial and osteoinductive capabilities in this study, which exhibit effective catalytic power for Fenton‐like reaction and controllable ion release behavior. This research offers a novel and promising treatment strategy for IAOM.</description><subject>Alkaline phosphatase</subject><subject>antibacteria</subject><subject>Antibiotics</subject><subject>Bone growth</subject><subject>Bone implants</subject><subject>Calcification</subject><subject>Cell proliferation</subject><subject>chemodynamic therapy</subject><subject>Copper</subject><subject>Drug resistance</subject><subject>Extracellular matrix</subject><subject>Gene expression</subject><subject>Hydrogen peroxide</subject><subject>Hydroxyl radicals</subject><subject>implant‐associated osteomyelitis</subject><subject>metal peroxide</subject><subject>Microenvironments</subject><subject>Nanoparticles</subject><subject>Osteogenesis</subject><subject>Osteomyelitis</subject><subject>Polyethylene glycol</subject><subject>Regeneration</subject><subject>Regeneration (physiology)</subject><subject>Strontium</subject><issn>2192-2640</issn><issn>2192-2659</issn><issn>2192-2659</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkL9OIzEQhy10CFCgpUQr0VyT3Njefy6jcByRiEAICirLa8_eOdpdB3v3uHQ8As_Ik2AULkg0TDEzxTc_jT5CjilMKAD7ocyfdsKAceAZEzvkgFHBxizPxLftnsI-OQphCbHyjOYl3SP7vEw5AIUDcn-DrTPY2O53srDaO-z-Wu-6Frs-qZ1P5u2qUV3_8vQ8DcFpq3o0yVXo0bXreNbbkFTr5GxQTbLAPvZr9O6fNXhIdmvVBDx6nyNyd_7zdnYxvrz6NZ9NL8eaF1yMK5PTWikuqFam0AIqyHmqhdaVBpWWWQmoa45UG5EZpSuTQplVlVAlL3Sp-Ih83-SuvHsYMPSytUFjE79GNwTJBE9ZkYuMRvT0E7p0g-_id5JDQXMBoigjNdlQ0UYIHmu58rZVfi0pyDfv8s273HqPByfvsUPVotni_y1HQGyAR9vg-os4OT27WHyEvwI2QpDn</recordid><startdate>20240601</startdate><enddate>20240601</enddate><creator>Guan, Xin</creator><creator>Wu, Siyuan</creator><creator>Ouyang, Sixue</creator><creator>Ren, Shuchen</creator><creator>Cui, Naiqian</creator><creator>Wu, Xiaohu</creator><creator>Xiang, Dayong</creator><creator>Chen, Wenting</creator><creator>Yu, Bin</creator><creator>Zhao, Peng</creator><creator>Wang, Bowei</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T5</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7TO</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6914-0605</orcidid></search><sort><creationdate>20240601</creationdate><title>Remodeling Microenvironment for Implant‐Associated Osteomyelitis by Dual Metal Peroxide</title><author>Guan, Xin ; Wu, Siyuan ; Ouyang, Sixue ; Ren, Shuchen ; Cui, Naiqian ; Wu, Xiaohu ; Xiang, Dayong ; Chen, Wenting ; Yu, Bin ; Zhao, Peng ; Wang, Bowei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3739-bd61faa391cad7c90b0634c9ccbc0a48580ecf3e1cd95dacbd4085bb9a837c8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Alkaline phosphatase</topic><topic>antibacteria</topic><topic>Antibiotics</topic><topic>Bone growth</topic><topic>Bone implants</topic><topic>Calcification</topic><topic>Cell proliferation</topic><topic>chemodynamic therapy</topic><topic>Copper</topic><topic>Drug resistance</topic><topic>Extracellular matrix</topic><topic>Gene expression</topic><topic>Hydrogen peroxide</topic><topic>Hydroxyl radicals</topic><topic>implant‐associated osteomyelitis</topic><topic>metal peroxide</topic><topic>Microenvironments</topic><topic>Nanoparticles</topic><topic>Osteogenesis</topic><topic>Osteomyelitis</topic><topic>Polyethylene glycol</topic><topic>Regeneration</topic><topic>Regeneration (physiology)</topic><topic>Strontium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guan, Xin</creatorcontrib><creatorcontrib>Wu, Siyuan</creatorcontrib><creatorcontrib>Ouyang, Sixue</creatorcontrib><creatorcontrib>Ren, Shuchen</creatorcontrib><creatorcontrib>Cui, Naiqian</creatorcontrib><creatorcontrib>Wu, Xiaohu</creatorcontrib><creatorcontrib>Xiang, Dayong</creatorcontrib><creatorcontrib>Chen, Wenting</creatorcontrib><creatorcontrib>Yu, Bin</creatorcontrib><creatorcontrib>Zhao, Peng</creatorcontrib><creatorcontrib>Wang, Bowei</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Immunology Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>MEDLINE - Academic</collection><jtitle>Advanced healthcare materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guan, Xin</au><au>Wu, Siyuan</au><au>Ouyang, Sixue</au><au>Ren, Shuchen</au><au>Cui, Naiqian</au><au>Wu, Xiaohu</au><au>Xiang, Dayong</au><au>Chen, Wenting</au><au>Yu, Bin</au><au>Zhao, Peng</au><au>Wang, Bowei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Remodeling Microenvironment for Implant‐Associated Osteomyelitis by Dual Metal Peroxide</atitle><jtitle>Advanced healthcare materials</jtitle><addtitle>Adv Healthc Mater</addtitle><date>2024-06-01</date><risdate>2024</risdate><volume>13</volume><issue>16</issue><spage>e2303529</spage><epage>n/a</epage><pages>e2303529-n/a</pages><issn>2192-2640</issn><issn>2192-2659</issn><eissn>2192-2659</eissn><abstract>Implant‐associated osteomyelitis (IAOM) is characterized by bone infection and destruction; current therapy of antibiotic treatment and surgical debridement often results in drug resistance and bone defect. It is challenging to develop an antibiotic‐free bactericidal and osteogenic‐enhanced strategy for IAOM. Herein, an IAOM‐tailored antibacterial and osteoinductive composite of copper (Cu)–strontium (Sr) peroxide nanoparticles (CSp NPs), encapsulated in polyethylene glycol diacrylate (PEGDA) (CSp@PEGDA), is designed. The dual functional CSp NPs display hydrogen peroxide (H2O2) self‐supplying and Fenton catalytic Cu2+ ions’ release, generating plenty of hydroxyl radical (•OH) in a pH‐responsive manner for bacterial killing, while the released Sr2+ promotes the in vitro osteogenicity regarding cell proliferation, alkaline phosphatase activity, extracellular matrix calcification, and osteo‐associated genes expression. The integration of Cu2+ and Sr2+ in CSp NPs together with the coated PEGDA hydrogel ensures the stable and sustainable ion release during short‐ and long‐term periods. Benefitted from the injectablity and photo‐crosslink ability, CSp@PEGDA is able to thoroughly fill the infectious site and gelate in situ for bacterial elimination and bone regeneration, which is verified through in vivo evaluation using a clinical‐simulating IAOM mouse model. These favorable abilities of CSp@PEGDA precisely meet the multiple therapeutic needs and pave a promising way for implant‐associated osteomyelitis treatment.
Copper–strontium peroxide nanoparticle‐loaded polyethylene glycol diacrylate (PEGDA) composites tailored for implant‐associated osteomyelitis (IAOM) are constructed with outstanding antibacterial and osteoinductive capabilities in this study, which exhibit effective catalytic power for Fenton‐like reaction and controllable ion release behavior. This research offers a novel and promising treatment strategy for IAOM.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38430010</pmid><doi>10.1002/adhm.202303529</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-6914-0605</orcidid></addata></record> |
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subjects | Alkaline phosphatase antibacteria Antibiotics Bone growth Bone implants Calcification Cell proliferation chemodynamic therapy Copper Drug resistance Extracellular matrix Gene expression Hydrogen peroxide Hydroxyl radicals implant‐associated osteomyelitis metal peroxide Microenvironments Nanoparticles Osteogenesis Osteomyelitis Polyethylene glycol Regeneration Regeneration (physiology) Strontium |
title | Remodeling Microenvironment for Implant‐Associated Osteomyelitis by Dual Metal Peroxide |
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