Bone regenerative efficacy of biphasic calcium phosphate collagen composite as a carrier of rhBMP-2
Objectives This study compared the bone regenerative effects of a recombinant human bone morphogenetic protein 2 (rhBMP‐2)‐loaded collagen‐based biphasic calcium phosphate composite (BCPC) and rhBMP‐2‐loaded biphasic calcium phosphate (BCP). Material and methods The in vitro release profiles of rhBM...
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Veröffentlicht in: | Clinical oral implants research 2016-11, Vol.27 (11), p.e91-e99 |
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creator | Lee, Eun-Ung Lim, Hyun-Chang Hong, Ji-Youn Lee, Jung-Seok Jung, Ui-Won Choi, Seong-Ho |
description | Objectives
This study compared the bone regenerative effects of a recombinant human bone morphogenetic protein 2 (rhBMP‐2)‐loaded collagen‐based biphasic calcium phosphate composite (BCPC) and rhBMP‐2‐loaded biphasic calcium phosphate (BCP).
Material and methods
The in vitro release profiles of rhBMP‐2‐loaded BCP and BCPC were measured. The animal surgery was performed on ten rabbits. Four 8‐mm‐diameter circular calvarial defects were made and filled with BCP, BCPC, rhBMP‐2‐loaded BCP (BMP + BCP) and rhBMP‐2‐loaded BCPC (BMP + BCPC). The animals were euthanized either 2 or 8 weeks after surgery.
Results
The initial burst release of rhBMP‐2 was greater for BCP than for BCPC, and both presented a slow release pattern thereafter. In rabbit calvarial defects, the space maintaining capability and graft resorption of all experimental groups did not show statistical differences at 2 and 8 weeks. New bone formation in the rhBMP‐2‐loaded groups was greater than in the non‐loaded groups at both weeks, but the amount of new bone was comparable between both rhBMP‐2‐loaded groups at both weeks. There was a distinct histologic difference between the BMP + BCP and BMP + BCPC groups at 2 weeks; the new bone formation occurred more in the intergranular spaces and the BCP‐to‐bone contact was greater in the BMP + BCPC group, but these differences were no longer discernible at 8 weeks.
Conclusions
BCP‐ and BCPC‐loaded rhBMP‐2 significantly improved bone regeneration and BCPC led to a dense network of new bone and bone particles during the early healing period. BCPC can therefore be considered as a promising candidate for carrying rhBMP‐2. |
doi_str_mv | 10.1111/clr.12568 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1837306057</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1837306057</sourcerecordid><originalsourceid>FETCH-LOGICAL-i4168-204649f5d0e05efaf514af55d9839a7776290a9a1b8d1a6e403417baa08136613</originalsourceid><addsrcrecordid>eNqNkU1vEzEQhq0KRNPCoX8ArcSFy7bj9df6SCNokQK0UNSj5TizxGU3u9jZtvn3nTSlB074YI_Gzzt6Z4axIw7HnM5JaNMxr5Su99iEa4ASFPAXbAIWVGm45vvsIOcbANC2tq_YPrFG1cJOWDjtV1gk_IUrTH4db7HAponBh03RN8U8DkufYyiCb0Mcu2JY9plSayxC37aeZBR0Q58jpXwuPJEpRUxbdVqefrkoq9fsZePbjG-e3kP289PHq-l5Oft29nn6YVZGyXVdViC1tI1aAILCxjeKS7rUwpJTb4zRlQVvPZ_XC-41ShCSm7n3UHOhNReH7P2u7pD6PyPmtetiDkg2V9iP2fFaGAEalPkPtKKKkqZE6Lt_0Jt-TCtqxFVbB9LI2hL19oka5x0u3JBi59PG_Z00ASc74C62uHn-5-C2K3S0Qve4QjedfX8MSFHuFDGv8f5Z4dNvp40wyl1_PXPix7WsruDSafEAYUmaTg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2034147489</pqid></control><display><type>article</type><title>Bone regenerative efficacy of biphasic calcium phosphate collagen composite as a carrier of rhBMP-2</title><source>Wiley Online Library - AutoHoldings Journals</source><source>MEDLINE</source><creator>Lee, Eun-Ung ; Lim, Hyun-Chang ; Hong, Ji-Youn ; Lee, Jung-Seok ; Jung, Ui-Won ; Choi, Seong-Ho</creator><creatorcontrib>Lee, Eun-Ung ; Lim, Hyun-Chang ; Hong, Ji-Youn ; Lee, Jung-Seok ; Jung, Ui-Won ; Choi, Seong-Ho</creatorcontrib><description>Objectives
This study compared the bone regenerative effects of a recombinant human bone morphogenetic protein 2 (rhBMP‐2)‐loaded collagen‐based biphasic calcium phosphate composite (BCPC) and rhBMP‐2‐loaded biphasic calcium phosphate (BCP).
Material and methods
The in vitro release profiles of rhBMP‐2‐loaded BCP and BCPC were measured. The animal surgery was performed on ten rabbits. Four 8‐mm‐diameter circular calvarial defects were made and filled with BCP, BCPC, rhBMP‐2‐loaded BCP (BMP + BCP) and rhBMP‐2‐loaded BCPC (BMP + BCPC). The animals were euthanized either 2 or 8 weeks after surgery.
Results
The initial burst release of rhBMP‐2 was greater for BCP than for BCPC, and both presented a slow release pattern thereafter. In rabbit calvarial defects, the space maintaining capability and graft resorption of all experimental groups did not show statistical differences at 2 and 8 weeks. New bone formation in the rhBMP‐2‐loaded groups was greater than in the non‐loaded groups at both weeks, but the amount of new bone was comparable between both rhBMP‐2‐loaded groups at both weeks. There was a distinct histologic difference between the BMP + BCP and BMP + BCPC groups at 2 weeks; the new bone formation occurred more in the intergranular spaces and the BCP‐to‐bone contact was greater in the BMP + BCPC group, but these differences were no longer discernible at 8 weeks.
Conclusions
BCP‐ and BCPC‐loaded rhBMP‐2 significantly improved bone regeneration and BCPC led to a dense network of new bone and bone particles during the early healing period. BCPC can therefore be considered as a promising candidate for carrying rhBMP‐2.</description><identifier>ISSN: 0905-7161</identifier><identifier>EISSN: 1600-0501</identifier><identifier>DOI: 10.1111/clr.12568</identifier><identifier>PMID: 25675839</identifier><language>eng</language><publisher>Denmark: Blackwell Publishing Ltd</publisher><subject>Animals ; biphasic calcium phosphate ; Bone growth ; Bone healing ; Bone morphogenetic protein 2 ; Bone Morphogenetic Protein 2 - pharmacology ; bone regeneration ; Bone Regeneration - drug effects ; bone substitutes ; Bone Substitutes - pharmacology ; Calcium ; Calcium phosphates ; Calcium Phosphates - pharmacology ; Collagen ; Collagen - pharmacology ; Defects ; Dentistry ; Drug Carriers ; In vitro methods and tests ; Models, Animal ; Osteogenesis ; Rabbits ; Recombinant Proteins - pharmacology ; Regeneration ; Regeneration (physiology) ; Skull - surgery ; Surgery ; Transforming Growth Factor beta - pharmacology</subject><ispartof>Clinical oral implants research, 2016-11, Vol.27 (11), p.e91-e99</ispartof><rights>2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2016 John Wiley & Sons A/S</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fclr.12568$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fclr.12568$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25675839$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Eun-Ung</creatorcontrib><creatorcontrib>Lim, Hyun-Chang</creatorcontrib><creatorcontrib>Hong, Ji-Youn</creatorcontrib><creatorcontrib>Lee, Jung-Seok</creatorcontrib><creatorcontrib>Jung, Ui-Won</creatorcontrib><creatorcontrib>Choi, Seong-Ho</creatorcontrib><title>Bone regenerative efficacy of biphasic calcium phosphate collagen composite as a carrier of rhBMP-2</title><title>Clinical oral implants research</title><addtitle>Clin. Oral Impl. Res</addtitle><description>Objectives
This study compared the bone regenerative effects of a recombinant human bone morphogenetic protein 2 (rhBMP‐2)‐loaded collagen‐based biphasic calcium phosphate composite (BCPC) and rhBMP‐2‐loaded biphasic calcium phosphate (BCP).
Material and methods
The in vitro release profiles of rhBMP‐2‐loaded BCP and BCPC were measured. The animal surgery was performed on ten rabbits. Four 8‐mm‐diameter circular calvarial defects were made and filled with BCP, BCPC, rhBMP‐2‐loaded BCP (BMP + BCP) and rhBMP‐2‐loaded BCPC (BMP + BCPC). The animals were euthanized either 2 or 8 weeks after surgery.
Results
The initial burst release of rhBMP‐2 was greater for BCP than for BCPC, and both presented a slow release pattern thereafter. In rabbit calvarial defects, the space maintaining capability and graft resorption of all experimental groups did not show statistical differences at 2 and 8 weeks. New bone formation in the rhBMP‐2‐loaded groups was greater than in the non‐loaded groups at both weeks, but the amount of new bone was comparable between both rhBMP‐2‐loaded groups at both weeks. There was a distinct histologic difference between the BMP + BCP and BMP + BCPC groups at 2 weeks; the new bone formation occurred more in the intergranular spaces and the BCP‐to‐bone contact was greater in the BMP + BCPC group, but these differences were no longer discernible at 8 weeks.
Conclusions
BCP‐ and BCPC‐loaded rhBMP‐2 significantly improved bone regeneration and BCPC led to a dense network of new bone and bone particles during the early healing period. BCPC can therefore be considered as a promising candidate for carrying rhBMP‐2.</description><subject>Animals</subject><subject>biphasic calcium phosphate</subject><subject>Bone growth</subject><subject>Bone healing</subject><subject>Bone morphogenetic protein 2</subject><subject>Bone Morphogenetic Protein 2 - pharmacology</subject><subject>bone regeneration</subject><subject>Bone Regeneration - drug effects</subject><subject>bone substitutes</subject><subject>Bone Substitutes - pharmacology</subject><subject>Calcium</subject><subject>Calcium phosphates</subject><subject>Calcium Phosphates - pharmacology</subject><subject>Collagen</subject><subject>Collagen - pharmacology</subject><subject>Defects</subject><subject>Dentistry</subject><subject>Drug Carriers</subject><subject>In vitro methods and tests</subject><subject>Models, Animal</subject><subject>Osteogenesis</subject><subject>Rabbits</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Regeneration</subject><subject>Regeneration (physiology)</subject><subject>Skull - surgery</subject><subject>Surgery</subject><subject>Transforming Growth Factor beta - pharmacology</subject><issn>0905-7161</issn><issn>1600-0501</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1vEzEQhq0KRNPCoX8ArcSFy7bj9df6SCNokQK0UNSj5TizxGU3u9jZtvn3nTSlB074YI_Gzzt6Z4axIw7HnM5JaNMxr5Su99iEa4ASFPAXbAIWVGm45vvsIOcbANC2tq_YPrFG1cJOWDjtV1gk_IUrTH4db7HAponBh03RN8U8DkufYyiCb0Mcu2JY9plSayxC37aeZBR0Q58jpXwuPJEpRUxbdVqefrkoq9fsZePbjG-e3kP289PHq-l5Oft29nn6YVZGyXVdViC1tI1aAILCxjeKS7rUwpJTb4zRlQVvPZ_XC-41ShCSm7n3UHOhNReH7P2u7pD6PyPmtetiDkg2V9iP2fFaGAEalPkPtKKKkqZE6Lt_0Jt-TCtqxFVbB9LI2hL19oka5x0u3JBi59PG_Z00ASc74C62uHn-5-C2K3S0Qve4QjedfX8MSFHuFDGv8f5Z4dNvp40wyl1_PXPix7WsruDSafEAYUmaTg</recordid><startdate>201611</startdate><enddate>201611</enddate><creator>Lee, Eun-Ung</creator><creator>Lim, Hyun-Chang</creator><creator>Hong, Ji-Youn</creator><creator>Lee, Jung-Seok</creator><creator>Jung, Ui-Won</creator><creator>Choi, Seong-Ho</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QO</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201611</creationdate><title>Bone regenerative efficacy of biphasic calcium phosphate collagen composite as a carrier of rhBMP-2</title><author>Lee, Eun-Ung ; Lim, Hyun-Chang ; Hong, Ji-Youn ; Lee, Jung-Seok ; Jung, Ui-Won ; Choi, Seong-Ho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i4168-204649f5d0e05efaf514af55d9839a7776290a9a1b8d1a6e403417baa08136613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>biphasic calcium phosphate</topic><topic>Bone growth</topic><topic>Bone healing</topic><topic>Bone morphogenetic protein 2</topic><topic>Bone Morphogenetic Protein 2 - pharmacology</topic><topic>bone regeneration</topic><topic>Bone Regeneration - drug effects</topic><topic>bone substitutes</topic><topic>Bone Substitutes - pharmacology</topic><topic>Calcium</topic><topic>Calcium phosphates</topic><topic>Calcium Phosphates - pharmacology</topic><topic>Collagen</topic><topic>Collagen - pharmacology</topic><topic>Defects</topic><topic>Dentistry</topic><topic>Drug Carriers</topic><topic>In vitro methods and tests</topic><topic>Models, Animal</topic><topic>Osteogenesis</topic><topic>Rabbits</topic><topic>Recombinant Proteins - pharmacology</topic><topic>Regeneration</topic><topic>Regeneration (physiology)</topic><topic>Skull - surgery</topic><topic>Surgery</topic><topic>Transforming Growth Factor beta - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Eun-Ung</creatorcontrib><creatorcontrib>Lim, Hyun-Chang</creatorcontrib><creatorcontrib>Hong, Ji-Youn</creatorcontrib><creatorcontrib>Lee, Jung-Seok</creatorcontrib><creatorcontrib>Jung, Ui-Won</creatorcontrib><creatorcontrib>Choi, Seong-Ho</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical oral implants research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Eun-Ung</au><au>Lim, Hyun-Chang</au><au>Hong, Ji-Youn</au><au>Lee, Jung-Seok</au><au>Jung, Ui-Won</au><au>Choi, Seong-Ho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bone regenerative efficacy of biphasic calcium phosphate collagen composite as a carrier of rhBMP-2</atitle><jtitle>Clinical oral implants research</jtitle><addtitle>Clin. Oral Impl. Res</addtitle><date>2016-11</date><risdate>2016</risdate><volume>27</volume><issue>11</issue><spage>e91</spage><epage>e99</epage><pages>e91-e99</pages><issn>0905-7161</issn><eissn>1600-0501</eissn><abstract>Objectives
This study compared the bone regenerative effects of a recombinant human bone morphogenetic protein 2 (rhBMP‐2)‐loaded collagen‐based biphasic calcium phosphate composite (BCPC) and rhBMP‐2‐loaded biphasic calcium phosphate (BCP).
Material and methods
The in vitro release profiles of rhBMP‐2‐loaded BCP and BCPC were measured. The animal surgery was performed on ten rabbits. Four 8‐mm‐diameter circular calvarial defects were made and filled with BCP, BCPC, rhBMP‐2‐loaded BCP (BMP + BCP) and rhBMP‐2‐loaded BCPC (BMP + BCPC). The animals were euthanized either 2 or 8 weeks after surgery.
Results
The initial burst release of rhBMP‐2 was greater for BCP than for BCPC, and both presented a slow release pattern thereafter. In rabbit calvarial defects, the space maintaining capability and graft resorption of all experimental groups did not show statistical differences at 2 and 8 weeks. New bone formation in the rhBMP‐2‐loaded groups was greater than in the non‐loaded groups at both weeks, but the amount of new bone was comparable between both rhBMP‐2‐loaded groups at both weeks. There was a distinct histologic difference between the BMP + BCP and BMP + BCPC groups at 2 weeks; the new bone formation occurred more in the intergranular spaces and the BCP‐to‐bone contact was greater in the BMP + BCPC group, but these differences were no longer discernible at 8 weeks.
Conclusions
BCP‐ and BCPC‐loaded rhBMP‐2 significantly improved bone regeneration and BCPC led to a dense network of new bone and bone particles during the early healing period. BCPC can therefore be considered as a promising candidate for carrying rhBMP‐2.</abstract><cop>Denmark</cop><pub>Blackwell Publishing Ltd</pub><pmid>25675839</pmid><doi>10.1111/clr.12568</doi><tpages>9</tpages></addata></record> |
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subjects | Animals biphasic calcium phosphate Bone growth Bone healing Bone morphogenetic protein 2 Bone Morphogenetic Protein 2 - pharmacology bone regeneration Bone Regeneration - drug effects bone substitutes Bone Substitutes - pharmacology Calcium Calcium phosphates Calcium Phosphates - pharmacology Collagen Collagen - pharmacology Defects Dentistry Drug Carriers In vitro methods and tests Models, Animal Osteogenesis Rabbits Recombinant Proteins - pharmacology Regeneration Regeneration (physiology) Skull - surgery Surgery Transforming Growth Factor beta - pharmacology |
title | Bone regenerative efficacy of biphasic calcium phosphate collagen composite as a carrier of rhBMP-2 |
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