A comparison of two biomaterial carriers for osteogenic protein-1 (BMP-7) in an ovine critical defect model
Critical size defects in ovine tibiae, stabilised with intramedullary interlocking nails, were used to assess whether the addition of carboxymethylcellulose to the standard osteogenic protein-1 (OP-1/BMP-7) implant would affect the implant's efficacy for bone regeneration. The biomaterial carri...
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Veröffentlicht in: | Journal of bone and joint surgery. British volume 2006-07, Vol.88 (7), p.960-966 |
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description | Critical size defects in ovine tibiae, stabilised with intramedullary interlocking nails, were used to assess whether the addition of carboxymethylcellulose to the standard osteogenic protein-1 (OP-1/BMP-7) implant would affect the implant's efficacy for bone regeneration. The biomaterial carriers were a 'putty' carrier of carboxymethylcellulose and bovine-derived type-I collagen (OPP) or the standard with collagen alone (OPC). These two treatments were also compared to "ungrafted" negative controls. Efficacy of regeneration was determined using radiological, biomechanical and histological evaluations after four months of healing. The defects, filled with OPP and OPC, demonstrated radiodense material spanning the defect after one month of healing, with radiographic evidence of recorticalisation and remodelling by two months. The OPP and OPC treatment groups had equivalent structural and material properties that were significantly greater than those in the ungrafted controls. The structural properties of the OPP- and OPC-treated limbs were equivalent to those of the contralateral untreated limb (p > 0.05), yet material properties were inferior (p < 0.05). Histopathology revealed no residual inflammatory response to the biomaterial carriers or OP-1. The OPP- and OPC-treated animals had 60% to 85% lamellar bone within the defect, and less than 25% of the regenerate was composed of fibrous tissue. The defects in the untreated control animals contained less than 40% lamellar bone and more than 60% was fibrous tissue, creating full cortical thickness defects. In our studies carboxymethylcellulose did not adversely affect the capacity of the standard OP-1 implant for regenerating bone. |
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The biomaterial carriers were a 'putty' carrier of carboxymethylcellulose and bovine-derived type-I collagen (OPP) or the standard with collagen alone (OPC). These two treatments were also compared to "ungrafted" negative controls. Efficacy of regeneration was determined using radiological, biomechanical and histological evaluations after four months of healing. The defects, filled with OPP and OPC, demonstrated radiodense material spanning the defect after one month of healing, with radiographic evidence of recorticalisation and remodelling by two months. The OPP and OPC treatment groups had equivalent structural and material properties that were significantly greater than those in the ungrafted controls. The structural properties of the OPP- and OPC-treated limbs were equivalent to those of the contralateral untreated limb (p > 0.05), yet material properties were inferior (p < 0.05). Histopathology revealed no residual inflammatory response to the biomaterial carriers or OP-1. The OPP- and OPC-treated animals had 60% to 85% lamellar bone within the defect, and less than 25% of the regenerate was composed of fibrous tissue. The defects in the untreated control animals contained less than 40% lamellar bone and more than 60% was fibrous tissue, creating full cortical thickness defects. In our studies carboxymethylcellulose did not adversely affect the capacity of the standard OP-1 implant for regenerating bone.</description><edition>British volume</edition><identifier>ISSN: 0301-620X</identifier><identifier>ISSN: 2049-4394</identifier><identifier>EISSN: 2044-5377</identifier><identifier>EISSN: 2049-4408</identifier><identifier>DOI: 10.1302/0301-620X.88B7.17056</identifier><identifier>PMID: 16799005</identifier><identifier>CODEN: JBSUAK</identifier><language>eng</language><publisher>England: British Editorial Society of Bone & Joint Surgery</publisher><subject><![CDATA[Animals ; Biocompatible Materials - administration & dosage ; Biomechanical Phenomena ; Bone Diseases - drug therapy ; Bone Diseases - pathology ; Bone Diseases - physiopathology ; Bone Morphogenetic Protein 7 ; Bone Morphogenetic Proteins - administration & dosage ; Bone Regeneration - drug effects ; Carboxymethylcellulose Sodium - administration & dosage ; Collagen Type I - administration & dosage ; Disease Models, Animal ; Drug Carriers ; Drug Implants ; Female ; Radiography ; Recombinant Proteins - administration & dosage ; Sheep ; Tibia - diagnostic imaging ; Tibia - pathology ; Tibia - physiopathology ; Transforming Growth Factor beta - administration & dosage]]></subject><ispartof>Journal of bone and joint surgery. 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British volume</title><addtitle>J Bone Joint Surg Br</addtitle><description>Critical size defects in ovine tibiae, stabilised with intramedullary interlocking nails, were used to assess whether the addition of carboxymethylcellulose to the standard osteogenic protein-1 (OP-1/BMP-7) implant would affect the implant's efficacy for bone regeneration. The biomaterial carriers were a 'putty' carrier of carboxymethylcellulose and bovine-derived type-I collagen (OPP) or the standard with collagen alone (OPC). These two treatments were also compared to "ungrafted" negative controls. Efficacy of regeneration was determined using radiological, biomechanical and histological evaluations after four months of healing. The defects, filled with OPP and OPC, demonstrated radiodense material spanning the defect after one month of healing, with radiographic evidence of recorticalisation and remodelling by two months. The OPP and OPC treatment groups had equivalent structural and material properties that were significantly greater than those in the ungrafted controls. The structural properties of the OPP- and OPC-treated limbs were equivalent to those of the contralateral untreated limb (p > 0.05), yet material properties were inferior (p < 0.05). Histopathology revealed no residual inflammatory response to the biomaterial carriers or OP-1. The OPP- and OPC-treated animals had 60% to 85% lamellar bone within the defect, and less than 25% of the regenerate was composed of fibrous tissue. The defects in the untreated control animals contained less than 40% lamellar bone and more than 60% was fibrous tissue, creating full cortical thickness defects. In our studies carboxymethylcellulose did not adversely affect the capacity of the standard OP-1 implant for regenerating bone.</description><subject>Animals</subject><subject>Biocompatible Materials - administration & dosage</subject><subject>Biomechanical Phenomena</subject><subject>Bone Diseases - drug therapy</subject><subject>Bone Diseases - pathology</subject><subject>Bone Diseases - physiopathology</subject><subject>Bone Morphogenetic Protein 7</subject><subject>Bone Morphogenetic Proteins - administration & dosage</subject><subject>Bone Regeneration - drug effects</subject><subject>Carboxymethylcellulose Sodium - administration & dosage</subject><subject>Collagen Type I - administration & dosage</subject><subject>Disease Models, Animal</subject><subject>Drug Carriers</subject><subject>Drug Implants</subject><subject>Female</subject><subject>Radiography</subject><subject>Recombinant Proteins - administration & dosage</subject><subject>Sheep</subject><subject>Tibia - diagnostic imaging</subject><subject>Tibia - pathology</subject><subject>Tibia - physiopathology</subject><subject>Transforming Growth Factor beta - administration & dosage</subject><issn>0301-620X</issn><issn>2049-4394</issn><issn>2044-5377</issn><issn>2049-4408</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtLJDEURoM42O3jH4gEF6KLam9elWTZio8BB10ouAupVEqiVZU2qR6Zf2-13Tgwm1lduJzv414OQocEZoQBPQcGpCgpPM-UupAzIkGUW2hKgfNCMCm30fQbmaDdnF8BgAvBdtCElFJrADFFb3PsYrewKeTY49jg4SPiKsTODj4F22JnUwo-ZdzEhGMefHzxfXB4keLgQ18QfHrx66GQZzj02I4Vv0PvsUthCG6M177xbsBdrH27j340ts3-YDP30NP11ePlbXF3f_Pzcn5XOFayoahFxRUnijleW-DArauFbppSUwolJXUjbQVU0Jowohy1XEtBaTVuPBdasz10su4db3xf-jyYLmTn29b2Pi6zKZWQgjD1X5BoIZXgYgSP_wFf4zL14xOGUi2VJpSMEF9DLsWck2_MIoXOpj-GgFkpMysfZuXDrJSZL2Vj7GjTvaw6X_8NbRyxT5kdj3M</recordid><startdate>200607</startdate><enddate>200607</enddate><creator>Pluhar, G E</creator><creator>Turner, A S</creator><creator>Pierce, A R</creator><creator>Toth, C A</creator><creator>Wheeler, D L</creator><general>British Editorial Society of Bone & Joint Surgery</general><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>K9.</scope><scope>NAPCQ</scope><scope>7QP</scope><scope>7X8</scope></search><sort><creationdate>200607</creationdate><title>A comparison of two biomaterial carriers for osteogenic protein-1 (BMP-7) in an ovine critical defect model</title><author>Pluhar, G E ; Turner, A S ; Pierce, A R ; Toth, C A ; Wheeler, D L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c363t-d5b484183c4da0404acd59ff69220621df7ab0252d1318c2a497522b252e45993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Biocompatible Materials - administration & dosage</topic><topic>Biomechanical Phenomena</topic><topic>Bone Diseases - drug therapy</topic><topic>Bone Diseases - pathology</topic><topic>Bone Diseases - physiopathology</topic><topic>Bone Morphogenetic Protein 7</topic><topic>Bone Morphogenetic Proteins - administration & dosage</topic><topic>Bone Regeneration - drug effects</topic><topic>Carboxymethylcellulose Sodium - administration & dosage</topic><topic>Collagen Type I - administration & dosage</topic><topic>Disease Models, Animal</topic><topic>Drug Carriers</topic><topic>Drug Implants</topic><topic>Female</topic><topic>Radiography</topic><topic>Recombinant Proteins - administration & dosage</topic><topic>Sheep</topic><topic>Tibia - diagnostic imaging</topic><topic>Tibia - pathology</topic><topic>Tibia - physiopathology</topic><topic>Transforming Growth Factor beta - administration & dosage</topic><toplevel>online_resources</toplevel><creatorcontrib>Pluhar, G E</creatorcontrib><creatorcontrib>Turner, A S</creatorcontrib><creatorcontrib>Pierce, A R</creatorcontrib><creatorcontrib>Toth, C A</creatorcontrib><creatorcontrib>Wheeler, D L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of bone and joint surgery. British volume</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pluhar, G E</au><au>Turner, A S</au><au>Pierce, A R</au><au>Toth, C A</au><au>Wheeler, D L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A comparison of two biomaterial carriers for osteogenic protein-1 (BMP-7) in an ovine critical defect model</atitle><jtitle>Journal of bone and joint surgery. British volume</jtitle><addtitle>J Bone Joint Surg Br</addtitle><date>2006-07</date><risdate>2006</risdate><volume>88</volume><issue>7</issue><spage>960</spage><epage>966</epage><pages>960-966</pages><issn>0301-620X</issn><issn>2049-4394</issn><eissn>2044-5377</eissn><eissn>2049-4408</eissn><coden>JBSUAK</coden><abstract>Critical size defects in ovine tibiae, stabilised with intramedullary interlocking nails, were used to assess whether the addition of carboxymethylcellulose to the standard osteogenic protein-1 (OP-1/BMP-7) implant would affect the implant's efficacy for bone regeneration. The biomaterial carriers were a 'putty' carrier of carboxymethylcellulose and bovine-derived type-I collagen (OPP) or the standard with collagen alone (OPC). These two treatments were also compared to "ungrafted" negative controls. Efficacy of regeneration was determined using radiological, biomechanical and histological evaluations after four months of healing. The defects, filled with OPP and OPC, demonstrated radiodense material spanning the defect after one month of healing, with radiographic evidence of recorticalisation and remodelling by two months. The OPP and OPC treatment groups had equivalent structural and material properties that were significantly greater than those in the ungrafted controls. The structural properties of the OPP- and OPC-treated limbs were equivalent to those of the contralateral untreated limb (p > 0.05), yet material properties were inferior (p < 0.05). Histopathology revealed no residual inflammatory response to the biomaterial carriers or OP-1. The OPP- and OPC-treated animals had 60% to 85% lamellar bone within the defect, and less than 25% of the regenerate was composed of fibrous tissue. The defects in the untreated control animals contained less than 40% lamellar bone and more than 60% was fibrous tissue, creating full cortical thickness defects. In our studies carboxymethylcellulose did not adversely affect the capacity of the standard OP-1 implant for regenerating bone.</abstract><cop>England</cop><pub>British Editorial Society of Bone & Joint Surgery</pub><pmid>16799005</pmid><doi>10.1302/0301-620X.88B7.17056</doi><tpages>7</tpages><edition>British volume</edition></addata></record> |
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subjects | Animals Biocompatible Materials - administration & dosage Biomechanical Phenomena Bone Diseases - drug therapy Bone Diseases - pathology Bone Diseases - physiopathology Bone Morphogenetic Protein 7 Bone Morphogenetic Proteins - administration & dosage Bone Regeneration - drug effects Carboxymethylcellulose Sodium - administration & dosage Collagen Type I - administration & dosage Disease Models, Animal Drug Carriers Drug Implants Female Radiography Recombinant Proteins - administration & dosage Sheep Tibia - diagnostic imaging Tibia - pathology Tibia - physiopathology Transforming Growth Factor beta - administration & dosage |
title | A comparison of two biomaterial carriers for osteogenic protein-1 (BMP-7) in an ovine critical defect model |
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