Initial bone tissue reactions of hydroxyapatite/collagen–(3‐glycidoxypropyl)trimethoxysilane injectable bone paste
We have previously reported that a novel bioresorbable self‐setting injectable bone paste composed of hydroxyapatite/collagen bone‐like nanocomposite (HAp/Col) and (3‐glycidoxypropyl)trimethoxysilane (GPTMS) was successfully prepared and was replaced with new bone within 3 months of implantation in...
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creator | Sato, Taira Shirosaki, Yuki Oshima, Sho Tsuru, Kanji Koyama, Yoshihisa Aizawa, Mamoru Kikuchi, Masanori |
description | We have previously reported that a novel bioresorbable self‐setting injectable bone paste composed of hydroxyapatite/collagen bone‐like nanocomposite (HAp/Col) and (3‐glycidoxypropyl)trimethoxysilane (GPTMS) was successfully prepared and was replaced with new bone within 3 months of implantation in defects created in porcine tibia. In this study, the HAp/Col‐GPTMS paste was implanted into bone defects in rat tibiae to investigate the initial kinetics and bone tissue response. Even though more than 35% of GPTMS molecules should be eluted rapidly from directly injected pastes according to previously reported cell culture tests, in this study, energy‐dispersive X‐ray spectrometry did not detect Si (GPTMS) deposition in tissues surrounding the paste at 1 day postimplantation. Further, no abnormal inflammatory responses were observed in the surrounding tissues over the test period for both directly injected and prehardened pastes. Companying these observations with the results of the previous animal test (in which the paste was fully resorbed and was substituted with new bone), the eluted GPTMS resolved in no harm in vivo from the initial to final (completely resorbed) stages. Material resorption rates calculated from X‐ray microcomputed tomography (μ‐CT) images decreased with increasing in GPTMS concentration. Histological observations indicated that tartrate‐resistant acid phosphatase (TRAP) active cells, (assumed to be osteoclasts), exist on the periphery of pastes. This result suggested that the paste was resorbed by osteoclasts in the same way as the HAp/Col. Since a good correlation was observed between TRAP active areas in histological sections and material resorption rate calculated from μ‐CT, the TRAP activity coverage ratio offers the possibility to estimate the osteoclastic resorption ratio of materials, which are replaced with bone via bone remodeling process. |
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In this study, the HAp/Col‐GPTMS paste was implanted into bone defects in rat tibiae to investigate the initial kinetics and bone tissue response. Even though more than 35% of GPTMS molecules should be eluted rapidly from directly injected pastes according to previously reported cell culture tests, in this study, energy‐dispersive X‐ray spectrometry did not detect Si (GPTMS) deposition in tissues surrounding the paste at 1 day postimplantation. Further, no abnormal inflammatory responses were observed in the surrounding tissues over the test period for both directly injected and prehardened pastes. Companying these observations with the results of the previous animal test (in which the paste was fully resorbed and was substituted with new bone), the eluted GPTMS resolved in no harm in vivo from the initial to final (completely resorbed) stages. Material resorption rates calculated from X‐ray microcomputed tomography (μ‐CT) images decreased with increasing in GPTMS concentration. Histological observations indicated that tartrate‐resistant acid phosphatase (TRAP) active cells, (assumed to be osteoclasts), exist on the periphery of pastes. This result suggested that the paste was resorbed by osteoclasts in the same way as the HAp/Col. Since a good correlation was observed between TRAP active areas in histological sections and material resorption rate calculated from μ‐CT, the TRAP activity coverage ratio offers the possibility to estimate the osteoclastic resorption ratio of materials, which are replaced with bone via bone remodeling process.</description><identifier>ISSN: 1552-4973</identifier><identifier>ISSN: 1552-4981</identifier><identifier>EISSN: 1552-4981</identifier><identifier>DOI: 10.1002/jbm.b.35451</identifier><identifier>PMID: 39052003</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>(3‐glycidoxypropyl)trimethoxysilane ; Acid phosphatase ; Acid phosphatase (tartrate-resistant) ; Acid resistance ; Animals ; Biocompatibility ; Biomedical materials ; bioresorbability evaluation ; Bone remodeling ; Bone resorption ; Bone Substitutes - chemistry ; Bone Substitutes - pharmacology ; bone tissue reaction ; Bones ; Cell culture ; Collagen ; Collagen - chemistry ; Computed tomography ; Defects ; Durapatite - chemistry ; Durapatite - pharmacology ; Hydroxyapatite ; hydroxyapatite/collagen ; In vivo methods and tests ; injectable bone paste ; Male ; Materials Testing ; Nanocomposites ; Nanocomposites - chemistry ; Osteoclasts ; Pastes ; Rats ; Rats, Sprague-Dawley ; Silanes - chemistry ; Silanes - pharmacology ; Spectrometry ; Swine ; Tibia ; Tibia - metabolism ; Tissue culture</subject><ispartof>Journal of biomedical materials research. 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Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3291-8a2ec55417d01b0f44d04c5fd18dab81c259c550697174c811d5b2fb7ab159af3</cites><orcidid>0000-0002-9451-8147</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%2Fjbm.b.35451$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjbm.b.35451$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39052003$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sato, Taira</creatorcontrib><creatorcontrib>Shirosaki, Yuki</creatorcontrib><creatorcontrib>Oshima, Sho</creatorcontrib><creatorcontrib>Tsuru, Kanji</creatorcontrib><creatorcontrib>Koyama, Yoshihisa</creatorcontrib><creatorcontrib>Aizawa, Mamoru</creatorcontrib><creatorcontrib>Kikuchi, Masanori</creatorcontrib><title>Initial bone tissue reactions of hydroxyapatite/collagen–(3‐glycidoxypropyl)trimethoxysilane injectable bone paste</title><title>Journal of biomedical materials research. Part B, Applied biomaterials</title><addtitle>J Biomed Mater Res B Appl Biomater</addtitle><description>We have previously reported that a novel bioresorbable self‐setting injectable bone paste composed of hydroxyapatite/collagen bone‐like nanocomposite (HAp/Col) and (3‐glycidoxypropyl)trimethoxysilane (GPTMS) was successfully prepared and was replaced with new bone within 3 months of implantation in defects created in porcine tibia. In this study, the HAp/Col‐GPTMS paste was implanted into bone defects in rat tibiae to investigate the initial kinetics and bone tissue response. Even though more than 35% of GPTMS molecules should be eluted rapidly from directly injected pastes according to previously reported cell culture tests, in this study, energy‐dispersive X‐ray spectrometry did not detect Si (GPTMS) deposition in tissues surrounding the paste at 1 day postimplantation. Further, no abnormal inflammatory responses were observed in the surrounding tissues over the test period for both directly injected and prehardened pastes. Companying these observations with the results of the previous animal test (in which the paste was fully resorbed and was substituted with new bone), the eluted GPTMS resolved in no harm in vivo from the initial to final (completely resorbed) stages. Material resorption rates calculated from X‐ray microcomputed tomography (μ‐CT) images decreased with increasing in GPTMS concentration. Histological observations indicated that tartrate‐resistant acid phosphatase (TRAP) active cells, (assumed to be osteoclasts), exist on the periphery of pastes. This result suggested that the paste was resorbed by osteoclasts in the same way as the HAp/Col. Since a good correlation was observed between TRAP active areas in histological sections and material resorption rate calculated from μ‐CT, the TRAP activity coverage ratio offers the possibility to estimate the osteoclastic resorption ratio of materials, which are replaced with bone via bone remodeling process.</description><subject>(3‐glycidoxypropyl)trimethoxysilane</subject><subject>Acid phosphatase</subject><subject>Acid phosphatase (tartrate-resistant)</subject><subject>Acid resistance</subject><subject>Animals</subject><subject>Biocompatibility</subject><subject>Biomedical materials</subject><subject>bioresorbability evaluation</subject><subject>Bone remodeling</subject><subject>Bone resorption</subject><subject>Bone Substitutes - chemistry</subject><subject>Bone Substitutes - pharmacology</subject><subject>bone tissue reaction</subject><subject>Bones</subject><subject>Cell culture</subject><subject>Collagen</subject><subject>Collagen - chemistry</subject><subject>Computed tomography</subject><subject>Defects</subject><subject>Durapatite - chemistry</subject><subject>Durapatite - pharmacology</subject><subject>Hydroxyapatite</subject><subject>hydroxyapatite/collagen</subject><subject>In vivo methods and tests</subject><subject>injectable bone paste</subject><subject>Male</subject><subject>Materials Testing</subject><subject>Nanocomposites</subject><subject>Nanocomposites - chemistry</subject><subject>Osteoclasts</subject><subject>Pastes</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Silanes - chemistry</subject><subject>Silanes - pharmacology</subject><subject>Spectrometry</subject><subject>Swine</subject><subject>Tibia</subject><subject>Tibia - metabolism</subject><subject>Tissue culture</subject><issn>1552-4973</issn><issn>1552-4981</issn><issn>1552-4981</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp9kctOxCAYRonReF-5N03caMyMXKd06Riv0bjRNQFKlQlTaqFqdz6CiW_ok4hWXbhwBYGTw_fzAbCF4BhBiA9maj5WY8IoQwtgFTGGR7TgaPF3n5MVsBbCLMETyMgyWCEFZBhCsgoez2sbrXSZ8rXJog2hM1lrpI7W1yHzVXbfl61_7mUjo43mQHvn5J2p31_edsn7y-ud67UtE9C0vundXmzt3MT7dBCsk8lp65nRUSpnhjcaGaLZAEuVdMFsfq_r4Pbk-ObobHR5fXp-dHg50gQXaMQlNpoxivISIgUrSktINatKxEupONKYFekeTooc5VRzhEqmcKVyqRArZEXWwe7gTekeOhOimNugjftM5rsgCOQ0zxHnk4Tu_EFnvmvrlC5RBSE45xOaqP2B0q0PoTWVaNLAsu0FguKzDpHqEEp81ZHo7W9np-am_GV__j8BeACerDP9fy5xMb2aDtYPe8mZkw</recordid><startdate>202408</startdate><enddate>202408</enddate><creator>Sato, Taira</creator><creator>Shirosaki, Yuki</creator><creator>Oshima, Sho</creator><creator>Tsuru, Kanji</creator><creator>Koyama, Yoshihisa</creator><creator>Aizawa, Mamoru</creator><creator>Kikuchi, Masanori</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</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>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9451-8147</orcidid></search><sort><creationdate>202408</creationdate><title>Initial bone tissue reactions of hydroxyapatite/collagen–(3‐glycidoxypropyl)trimethoxysilane injectable bone paste</title><author>Sato, Taira ; Shirosaki, Yuki ; Oshima, Sho ; Tsuru, Kanji ; Koyama, Yoshihisa ; Aizawa, Mamoru ; Kikuchi, Masanori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3291-8a2ec55417d01b0f44d04c5fd18dab81c259c550697174c811d5b2fb7ab159af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>(3‐glycidoxypropyl)trimethoxysilane</topic><topic>Acid phosphatase</topic><topic>Acid phosphatase (tartrate-resistant)</topic><topic>Acid resistance</topic><topic>Animals</topic><topic>Biocompatibility</topic><topic>Biomedical materials</topic><topic>bioresorbability evaluation</topic><topic>Bone remodeling</topic><topic>Bone resorption</topic><topic>Bone Substitutes - chemistry</topic><topic>Bone Substitutes - pharmacology</topic><topic>bone tissue reaction</topic><topic>Bones</topic><topic>Cell culture</topic><topic>Collagen</topic><topic>Collagen - chemistry</topic><topic>Computed tomography</topic><topic>Defects</topic><topic>Durapatite - chemistry</topic><topic>Durapatite - pharmacology</topic><topic>Hydroxyapatite</topic><topic>hydroxyapatite/collagen</topic><topic>In vivo methods and tests</topic><topic>injectable bone paste</topic><topic>Male</topic><topic>Materials Testing</topic><topic>Nanocomposites</topic><topic>Nanocomposites - chemistry</topic><topic>Osteoclasts</topic><topic>Pastes</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Silanes - chemistry</topic><topic>Silanes - pharmacology</topic><topic>Spectrometry</topic><topic>Swine</topic><topic>Tibia</topic><topic>Tibia - metabolism</topic><topic>Tissue culture</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sato, Taira</creatorcontrib><creatorcontrib>Shirosaki, Yuki</creatorcontrib><creatorcontrib>Oshima, Sho</creatorcontrib><creatorcontrib>Tsuru, Kanji</creatorcontrib><creatorcontrib>Koyama, Yoshihisa</creatorcontrib><creatorcontrib>Aizawa, Mamoru</creatorcontrib><creatorcontrib>Kikuchi, Masanori</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research 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>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</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>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>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biomedical materials research. Part B, Applied biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sato, Taira</au><au>Shirosaki, Yuki</au><au>Oshima, Sho</au><au>Tsuru, Kanji</au><au>Koyama, Yoshihisa</au><au>Aizawa, Mamoru</au><au>Kikuchi, Masanori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Initial bone tissue reactions of hydroxyapatite/collagen–(3‐glycidoxypropyl)trimethoxysilane injectable bone paste</atitle><jtitle>Journal of biomedical materials research. Part B, Applied biomaterials</jtitle><addtitle>J Biomed Mater Res B Appl Biomater</addtitle><date>2024-08</date><risdate>2024</risdate><volume>112</volume><issue>8</issue><spage>e35451</spage><epage>n/a</epage><pages>e35451-n/a</pages><issn>1552-4973</issn><issn>1552-4981</issn><eissn>1552-4981</eissn><abstract>We have previously reported that a novel bioresorbable self‐setting injectable bone paste composed of hydroxyapatite/collagen bone‐like nanocomposite (HAp/Col) and (3‐glycidoxypropyl)trimethoxysilane (GPTMS) was successfully prepared and was replaced with new bone within 3 months of implantation in defects created in porcine tibia. In this study, the HAp/Col‐GPTMS paste was implanted into bone defects in rat tibiae to investigate the initial kinetics and bone tissue response. Even though more than 35% of GPTMS molecules should be eluted rapidly from directly injected pastes according to previously reported cell culture tests, in this study, energy‐dispersive X‐ray spectrometry did not detect Si (GPTMS) deposition in tissues surrounding the paste at 1 day postimplantation. Further, no abnormal inflammatory responses were observed in the surrounding tissues over the test period for both directly injected and prehardened pastes. Companying these observations with the results of the previous animal test (in which the paste was fully resorbed and was substituted with new bone), the eluted GPTMS resolved in no harm in vivo from the initial to final (completely resorbed) stages. Material resorption rates calculated from X‐ray microcomputed tomography (μ‐CT) images decreased with increasing in GPTMS concentration. Histological observations indicated that tartrate‐resistant acid phosphatase (TRAP) active cells, (assumed to be osteoclasts), exist on the periphery of pastes. This result suggested that the paste was resorbed by osteoclasts in the same way as the HAp/Col. Since a good correlation was observed between TRAP active areas in histological sections and material resorption rate calculated from μ‐CT, the TRAP activity coverage ratio offers the possibility to estimate the osteoclastic resorption ratio of materials, which are replaced with bone via bone remodeling process.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>39052003</pmid><doi>10.1002/jbm.b.35451</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-9451-8147</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | (3‐glycidoxypropyl)trimethoxysilane Acid phosphatase Acid phosphatase (tartrate-resistant) Acid resistance Animals Biocompatibility Biomedical materials bioresorbability evaluation Bone remodeling Bone resorption Bone Substitutes - chemistry Bone Substitutes - pharmacology bone tissue reaction Bones Cell culture Collagen Collagen - chemistry Computed tomography Defects Durapatite - chemistry Durapatite - pharmacology Hydroxyapatite hydroxyapatite/collagen In vivo methods and tests injectable bone paste Male Materials Testing Nanocomposites Nanocomposites - chemistry Osteoclasts Pastes Rats Rats, Sprague-Dawley Silanes - chemistry Silanes - pharmacology Spectrometry Swine Tibia Tibia - metabolism Tissue culture |
title | Initial bone tissue reactions of hydroxyapatite/collagen–(3‐glycidoxypropyl)trimethoxysilane injectable bone paste |
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