The enhanced osteogenesis and osteointegration of 3-DP PCL scaffolds via structural and functional optimization using collagen networks
Optimal balance between biological activity and mechanical stability should be meticulously considered during scaffold design for bone tissue engineering applications. To fabricate an individualized construct with biomechanical and biological functionality for bone tissue regeneration, a polycaprola...
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Veröffentlicht in: | RSC advances 2018-01, Vol.8 (56), p.32304-32316 |
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description | Optimal balance between biological activity and mechanical stability should be meticulously considered during scaffold design for bone tissue engineering applications. To fabricate an individualized construct with biomechanical and biological functionality for bone tissue regeneration, a polycaprolactone-collagen (PCL-COL) composite construct was developed through the combination of three-dimensional printing (3-DP) technology and biomimetic collagen matrix incorporation, with a 3-DP PCL framework maintaining the mechanical stability and a porous collagen matrix improving the biological activity. The results indicate that the compressive modulus of the composite constructs increased synergistically (over 40 MPa), providing sufficient mechanical support during new bone formation. On the other hand, the collagen matrix with a micro-porous architecture structurally increased scaffold areas and provided cellular adhesion sites, allowing for the functional construction of a favorable 3D microenvironment for BMSC adhesion, proliferation and extracellular matrix production. Moreover, critical-sized long bone defect (CSD) implantation demonstrated that the optimized composite constructs could promote bone tissue regeneration (5.5-fold) and bone-material osteointegration (4.7-fold), and decrease fibrosis encapsulation, compared to pristine PCL. The results indicate that these biomimetically ornamented PCL-COL constructs exhibit favorable mechanical properties and biological functionality, demonstrating great potential as an effective bone graft substitute for bone defect treatment. Meanwhile, they can also harness the advantages of 3-DP technology and a collagen-based functionalized strategy, facilitating the creation of customized and functional PCL-COL constructs for clinical translation. |
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To fabricate an individualized construct with biomechanical and biological functionality for bone tissue regeneration, a polycaprolactone-collagen (PCL-COL) composite construct was developed through the combination of three-dimensional printing (3-DP) technology and biomimetic collagen matrix incorporation, with a 3-DP PCL framework maintaining the mechanical stability and a porous collagen matrix improving the biological activity. The results indicate that the compressive modulus of the composite constructs increased synergistically (over 40 MPa), providing sufficient mechanical support during new bone formation. On the other hand, the collagen matrix with a micro-porous architecture structurally increased scaffold areas and provided cellular adhesion sites, allowing for the functional construction of a favorable 3D microenvironment for BMSC adhesion, proliferation and extracellular matrix production. Moreover, critical-sized long bone defect (CSD) implantation demonstrated that the optimized composite constructs could promote bone tissue regeneration (5.5-fold) and bone-material osteointegration (4.7-fold), and decrease fibrosis encapsulation, compared to pristine PCL. The results indicate that these biomimetically ornamented PCL-COL constructs exhibit favorable mechanical properties and biological functionality, demonstrating great potential as an effective bone graft substitute for bone defect treatment. Meanwhile, they can also harness the advantages of 3-DP technology and a collagen-based functionalized strategy, facilitating the creation of customized and functional PCL-COL constructs for clinical translation.</description><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/c8ra05615c</identifier><identifier>PMID: 35547520</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Adhesion ; Biocompatibility ; Biological activity ; Biological effects ; Biological properties ; Biomechanical engineering ; Biomechanics ; Biomedical materials ; Biomimetics ; Bones ; Cellular structure ; Chemistry ; Collagen ; Design engineering ; Fibrosis ; Grafting ; Implantation ; Mechanical properties ; Modulus of elasticity ; Polycaprolactone ; Porous media ; Regeneration ; Scaffolds ; Stability ; Substitute bone ; Three dimensional printing ; Tissue engineering</subject><ispartof>RSC advances, 2018-01, Vol.8 (56), p.32304-32316</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2018</rights><rights>This journal is © The Royal Society of Chemistry 2018 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-9daaac4e44ac8ed85e24f52bd390ed2748ab9d04d35005341ca0817dedefe7ea3</citedby><cites>FETCH-LOGICAL-c406t-9daaac4e44ac8ed85e24f52bd390ed2748ab9d04d35005341ca0817dedefe7ea3</cites><orcidid>0000-0001-8433-7265</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086255/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086255/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,27907,27908,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35547520$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Jinbing</creatorcontrib><creatorcontrib>Lin, Chucheng</creatorcontrib><creatorcontrib>Gao, Xin</creatorcontrib><creatorcontrib>Zheng, Zhiwei</creatorcontrib><creatorcontrib>Lv, Mimgming</creatorcontrib><creatorcontrib>Sun, Jian</creatorcontrib><creatorcontrib>Zhang, Zhiyong</creatorcontrib><title>The enhanced osteogenesis and osteointegration of 3-DP PCL scaffolds via structural and functional optimization using collagen networks</title><title>RSC advances</title><addtitle>RSC Adv</addtitle><description>Optimal balance between biological activity and mechanical stability should be meticulously considered during scaffold design for bone tissue engineering applications. To fabricate an individualized construct with biomechanical and biological functionality for bone tissue regeneration, a polycaprolactone-collagen (PCL-COL) composite construct was developed through the combination of three-dimensional printing (3-DP) technology and biomimetic collagen matrix incorporation, with a 3-DP PCL framework maintaining the mechanical stability and a porous collagen matrix improving the biological activity. The results indicate that the compressive modulus of the composite constructs increased synergistically (over 40 MPa), providing sufficient mechanical support during new bone formation. On the other hand, the collagen matrix with a micro-porous architecture structurally increased scaffold areas and provided cellular adhesion sites, allowing for the functional construction of a favorable 3D microenvironment for BMSC adhesion, proliferation and extracellular matrix production. Moreover, critical-sized long bone defect (CSD) implantation demonstrated that the optimized composite constructs could promote bone tissue regeneration (5.5-fold) and bone-material osteointegration (4.7-fold), and decrease fibrosis encapsulation, compared to pristine PCL. The results indicate that these biomimetically ornamented PCL-COL constructs exhibit favorable mechanical properties and biological functionality, demonstrating great potential as an effective bone graft substitute for bone defect treatment. Meanwhile, they can also harness the advantages of 3-DP technology and a collagen-based functionalized strategy, facilitating the creation of customized and functional PCL-COL constructs for clinical translation.</description><subject>Adhesion</subject><subject>Biocompatibility</subject><subject>Biological activity</subject><subject>Biological effects</subject><subject>Biological properties</subject><subject>Biomechanical engineering</subject><subject>Biomechanics</subject><subject>Biomedical materials</subject><subject>Biomimetics</subject><subject>Bones</subject><subject>Cellular structure</subject><subject>Chemistry</subject><subject>Collagen</subject><subject>Design engineering</subject><subject>Fibrosis</subject><subject>Grafting</subject><subject>Implantation</subject><subject>Mechanical properties</subject><subject>Modulus of elasticity</subject><subject>Polycaprolactone</subject><subject>Porous media</subject><subject>Regeneration</subject><subject>Scaffolds</subject><subject>Stability</subject><subject>Substitute bone</subject><subject>Three dimensional printing</subject><subject>Tissue engineering</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdkd9qFDEUxoMottTe-AAS8EaE0fyfzI1QxqqFBYvU6yGbnNlNnU3WJNPSvoCvbdrdlmpukpP8zpcv-RB6TckHSnj30epkiFRU2mfokBGhGkZU9_zJ-gAd53xJ6lCSMkVfogMupWglI4foz8UaMIS1CRYcjrlAXEGA7DM2Yb_hQ4FVMsXHgOOIefP5HJ_3C5ytGcc4uYyvvMG5pNmWOZnpvnOcg73rqGXcFr_xtzuBOfuwwjZOk6kX4QDlOqZf-RV6MZopw_F-PkI_v5xe9N-axfevZ_3JorGCqNJ0zhhjBQhhrAanJTAxSrZ0vCPgWCu0WXaOCMclIZILag3RtHXgYIQWDD9Cn3a623m5AWchlOp42Ca_MelmiMYP_54Evx5W8WroiFZMyirwbi-Q4u8Zchk2PluozwkQ5zwwpUTbCa7air79D72Mc6o_UilKtOZcMFap9zvKpphzgvHRDCXDXcRDr3-c3EfcV_jNU_uP6EOg_C8xjaVM</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Wang, Jinbing</creator><creator>Lin, Chucheng</creator><creator>Gao, Xin</creator><creator>Zheng, Zhiwei</creator><creator>Lv, Mimgming</creator><creator>Sun, Jian</creator><creator>Zhang, Zhiyong</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8433-7265</orcidid></search><sort><creationdate>20180101</creationdate><title>The enhanced osteogenesis and osteointegration of 3-DP PCL scaffolds via structural and functional optimization using collagen networks</title><author>Wang, Jinbing ; Lin, Chucheng ; Gao, Xin ; Zheng, Zhiwei ; Lv, Mimgming ; Sun, Jian ; Zhang, Zhiyong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-9daaac4e44ac8ed85e24f52bd390ed2748ab9d04d35005341ca0817dedefe7ea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adhesion</topic><topic>Biocompatibility</topic><topic>Biological activity</topic><topic>Biological effects</topic><topic>Biological properties</topic><topic>Biomechanical engineering</topic><topic>Biomechanics</topic><topic>Biomedical materials</topic><topic>Biomimetics</topic><topic>Bones</topic><topic>Cellular structure</topic><topic>Chemistry</topic><topic>Collagen</topic><topic>Design engineering</topic><topic>Fibrosis</topic><topic>Grafting</topic><topic>Implantation</topic><topic>Mechanical properties</topic><topic>Modulus of elasticity</topic><topic>Polycaprolactone</topic><topic>Porous media</topic><topic>Regeneration</topic><topic>Scaffolds</topic><topic>Stability</topic><topic>Substitute bone</topic><topic>Three dimensional printing</topic><topic>Tissue engineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Jinbing</creatorcontrib><creatorcontrib>Lin, Chucheng</creatorcontrib><creatorcontrib>Gao, Xin</creatorcontrib><creatorcontrib>Zheng, Zhiwei</creatorcontrib><creatorcontrib>Lv, Mimgming</creatorcontrib><creatorcontrib>Sun, Jian</creatorcontrib><creatorcontrib>Zhang, Zhiyong</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Jinbing</au><au>Lin, Chucheng</au><au>Gao, Xin</au><au>Zheng, Zhiwei</au><au>Lv, Mimgming</au><au>Sun, Jian</au><au>Zhang, Zhiyong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The enhanced osteogenesis and osteointegration of 3-DP PCL scaffolds via structural and functional optimization using collagen networks</atitle><jtitle>RSC advances</jtitle><addtitle>RSC Adv</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>8</volume><issue>56</issue><spage>32304</spage><epage>32316</epage><pages>32304-32316</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>Optimal balance between biological activity and mechanical stability should be meticulously considered during scaffold design for bone tissue engineering applications. To fabricate an individualized construct with biomechanical and biological functionality for bone tissue regeneration, a polycaprolactone-collagen (PCL-COL) composite construct was developed through the combination of three-dimensional printing (3-DP) technology and biomimetic collagen matrix incorporation, with a 3-DP PCL framework maintaining the mechanical stability and a porous collagen matrix improving the biological activity. The results indicate that the compressive modulus of the composite constructs increased synergistically (over 40 MPa), providing sufficient mechanical support during new bone formation. On the other hand, the collagen matrix with a micro-porous architecture structurally increased scaffold areas and provided cellular adhesion sites, allowing for the functional construction of a favorable 3D microenvironment for BMSC adhesion, proliferation and extracellular matrix production. Moreover, critical-sized long bone defect (CSD) implantation demonstrated that the optimized composite constructs could promote bone tissue regeneration (5.5-fold) and bone-material osteointegration (4.7-fold), and decrease fibrosis encapsulation, compared to pristine PCL. The results indicate that these biomimetically ornamented PCL-COL constructs exhibit favorable mechanical properties and biological functionality, demonstrating great potential as an effective bone graft substitute for bone defect treatment. Meanwhile, they can also harness the advantages of 3-DP technology and a collagen-based functionalized strategy, facilitating the creation of customized and functional PCL-COL constructs for clinical translation.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>35547520</pmid><doi>10.1039/c8ra05615c</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-8433-7265</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adhesion Biocompatibility Biological activity Biological effects Biological properties Biomechanical engineering Biomechanics Biomedical materials Biomimetics Bones Cellular structure Chemistry Collagen Design engineering Fibrosis Grafting Implantation Mechanical properties Modulus of elasticity Polycaprolactone Porous media Regeneration Scaffolds Stability Substitute bone Three dimensional printing Tissue engineering |
title | The enhanced osteogenesis and osteointegration of 3-DP PCL scaffolds via structural and functional optimization using collagen networks |
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