Adhesion to chondroitinase ABC treated dentin
Dentin bonding relies on complete resin impregnation throughout the demineralised hydrophilic collagen mesh. Chondroitin sulphate‐glycosaminoglycans are claimed to regulate the three‐dimensional arrangement of the dentin organic matrix and its hydrophilicity. The aim of this study was to investigate...
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Veröffentlicht in: | Journal of biomedical materials research. Part B, Applied biomaterials Applied biomaterials, 2008-07, Vol.86B (1), p.228-236 |
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container_title | Journal of biomedical materials research. Part B, Applied biomaterials |
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creator | Mazzoni, Annalisa Pashley, David H. Ruggeri Jr, Alessandra Vita, Francesca Falconi, Mirella Di Lenarda, Roberto Breschi, Lorenzo |
description | Dentin bonding relies on complete resin impregnation throughout the demineralised hydrophilic collagen mesh. Chondroitin sulphate‐glycosaminoglycans are claimed to regulate the three‐dimensional arrangement of the dentin organic matrix and its hydrophilicity. The aim of this study was to investigate bond strength of two etch‐and‐rinse adhesives to chondroitinase ABC treated dentin. Human extracted molars were treated with chondroitinase ABC and a double labeling immunohistochemical technique was applied to reveal type I collagen and chondroitin 4/6 sulphate distribution under field emission in‐lens scanning electron microscope. The immunohistochemical technique confirmed the effective removal of chondroitin 4/6 sulphate after the enzymatic treatment. Dentin surfaces exposed to chondroitinase ABC and untreated specimens prepared on untreated acid‐etched dentin were bonded with Adper Scotchbond Multi‐Purpose or Prime and Bond NT. Bonded specimens were submitted to microtensile testing and nanoleakage interfacial analysis under transmission electron microscope. Increased mean values of microtensile bond strength and reduced nanoleakage expression were found for both adhesives after chondroitinase ABC treatment of the dentin surface. Adper Scotchbond Multi‐Purpose increased its bond strength about 28%, while bonding made with Prime and Bond NT almost doubled (92% increase) compared to untreated specimens. This study supports the hypothesis that adhesion can be enhanced by removal of chondroitin 4/6 sulphate and dermatan sulphate, probably due to a reduced amount of water content and enlarged interfibrillar spaces. Further studies should validate this hypothesis investigating the stability of chondroitin 4/6 and dermatan sulphate‐depleted dentin bonded interface over time. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008 |
doi_str_mv | 10.1002/jbm.b.31010 |
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Chondroitin sulphate‐glycosaminoglycans are claimed to regulate the three‐dimensional arrangement of the dentin organic matrix and its hydrophilicity. The aim of this study was to investigate bond strength of two etch‐and‐rinse adhesives to chondroitinase ABC treated dentin. Human extracted molars were treated with chondroitinase ABC and a double labeling immunohistochemical technique was applied to reveal type I collagen and chondroitin 4/6 sulphate distribution under field emission in‐lens scanning electron microscope. The immunohistochemical technique confirmed the effective removal of chondroitin 4/6 sulphate after the enzymatic treatment. Dentin surfaces exposed to chondroitinase ABC and untreated specimens prepared on untreated acid‐etched dentin were bonded with Adper Scotchbond Multi‐Purpose or Prime and Bond NT. Bonded specimens were submitted to microtensile testing and nanoleakage interfacial analysis under transmission electron microscope. Increased mean values of microtensile bond strength and reduced nanoleakage expression were found for both adhesives after chondroitinase ABC treatment of the dentin surface. Adper Scotchbond Multi‐Purpose increased its bond strength about 28%, while bonding made with Prime and Bond NT almost doubled (92% increase) compared to untreated specimens. This study supports the hypothesis that adhesion can be enhanced by removal of chondroitin 4/6 sulphate and dermatan sulphate, probably due to a reduced amount of water content and enlarged interfibrillar spaces. Further studies should validate this hypothesis investigating the stability of chondroitin 4/6 and dermatan sulphate‐depleted dentin bonded interface over time. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008</description><identifier>ISSN: 1552-4973</identifier><identifier>EISSN: 1552-4981</identifier><identifier>DOI: 10.1002/jbm.b.31010</identifier><identifier>PMID: 18161809</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Acid Etching, Dental - methods ; Chondroitin ABC Lyase - chemistry ; Dental Bonding - methods ; dental bonding systems ; dentin ; Dentin - chemistry ; Dentin-Bonding Agents - chemistry ; Dermatan Sulfate - chemistry ; Humans ; Immunohistochemistry - methods ; Materials Testing ; Microscopy, Electron, Transmission - methods ; microtensile bond strength ; proteoglycans ; Proteoglycans - chemistry ; Resin Cements - chemistry ; Stress, Mechanical ; Tensile Strength ; Water - chemistry</subject><ispartof>Journal of biomedical materials research. 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Part B, Applied biomaterials</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Dentin bonding relies on complete resin impregnation throughout the demineralised hydrophilic collagen mesh. Chondroitin sulphate‐glycosaminoglycans are claimed to regulate the three‐dimensional arrangement of the dentin organic matrix and its hydrophilicity. The aim of this study was to investigate bond strength of two etch‐and‐rinse adhesives to chondroitinase ABC treated dentin. Human extracted molars were treated with chondroitinase ABC and a double labeling immunohistochemical technique was applied to reveal type I collagen and chondroitin 4/6 sulphate distribution under field emission in‐lens scanning electron microscope. The immunohistochemical technique confirmed the effective removal of chondroitin 4/6 sulphate after the enzymatic treatment. Dentin surfaces exposed to chondroitinase ABC and untreated specimens prepared on untreated acid‐etched dentin were bonded with Adper Scotchbond Multi‐Purpose or Prime and Bond NT. Bonded specimens were submitted to microtensile testing and nanoleakage interfacial analysis under transmission electron microscope. Increased mean values of microtensile bond strength and reduced nanoleakage expression were found for both adhesives after chondroitinase ABC treatment of the dentin surface. Adper Scotchbond Multi‐Purpose increased its bond strength about 28%, while bonding made with Prime and Bond NT almost doubled (92% increase) compared to untreated specimens. This study supports the hypothesis that adhesion can be enhanced by removal of chondroitin 4/6 sulphate and dermatan sulphate, probably due to a reduced amount of water content and enlarged interfibrillar spaces. Further studies should validate this hypothesis investigating the stability of chondroitin 4/6 and dermatan sulphate‐depleted dentin bonded interface over time. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008</description><subject>Acid Etching, Dental - methods</subject><subject>Chondroitin ABC Lyase - chemistry</subject><subject>Dental Bonding - methods</subject><subject>dental bonding systems</subject><subject>dentin</subject><subject>Dentin - chemistry</subject><subject>Dentin-Bonding Agents - chemistry</subject><subject>Dermatan Sulfate - chemistry</subject><subject>Humans</subject><subject>Immunohistochemistry - methods</subject><subject>Materials Testing</subject><subject>Microscopy, Electron, Transmission - methods</subject><subject>microtensile bond strength</subject><subject>proteoglycans</subject><subject>Proteoglycans - chemistry</subject><subject>Resin Cements - chemistry</subject><subject>Stress, Mechanical</subject><subject>Tensile Strength</subject><subject>Water - chemistry</subject><issn>1552-4973</issn><issn>1552-4981</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0Eoh9w4o5y4oKyjOP464K0XUGhKoUDtBIXa5xMWZdsXOxsof8ewy4LXECyZMt-5hnbL2OPOMw4QPPsyq9mfiY4cLjD9rmUTd1aw-_u1lrssYOcrwqsQIr7bI8brrgBu8_qeb-kHOJYTbHqlnHsUwxTGDFTNT9aVFMinKivehrL7gN27xKHTA-38yH78PLF-8Wr-vTt8evF_LTuWgtQ-9a0kns0BrWUSNJIK7CRFgFRlQG9tz0oLjsNXhOhbYVWnSTogDyKQ_Z8471e-xX1XWmecHDXKaww3bqIwf19Moal-xRvnDDKWKOK4MlWkOKXNeXJrULuaBhwpLjOTtmmbVot_gsK0SilOS_g0w3YpZhzosvdbTi4Hzm4koPz7mcOhX785wN-s9uPLwDfAF_DQLf_crmToze_pPWmJuSJvu1qMH12Sgst3cXZsbt4d3J2DufKfRTfAT26oiY</recordid><startdate>200807</startdate><enddate>200807</enddate><creator>Mazzoni, Annalisa</creator><creator>Pashley, David H.</creator><creator>Ruggeri Jr, Alessandra</creator><creator>Vita, Francesca</creator><creator>Falconi, Mirella</creator><creator>Di Lenarda, Roberto</creator><creator>Breschi, Lorenzo</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200807</creationdate><title>Adhesion to chondroitinase ABC treated dentin</title><author>Mazzoni, Annalisa ; Pashley, David H. ; Ruggeri Jr, Alessandra ; Vita, Francesca ; Falconi, Mirella ; Di Lenarda, Roberto ; Breschi, Lorenzo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4900-b48451ba88a755ae58593a259a0aa6aa60db9d0615c70b7eea94376c5e0c0eba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acid Etching, Dental - methods</topic><topic>Chondroitin ABC Lyase - chemistry</topic><topic>Dental Bonding - methods</topic><topic>dental bonding systems</topic><topic>dentin</topic><topic>Dentin - chemistry</topic><topic>Dentin-Bonding Agents - chemistry</topic><topic>Dermatan Sulfate - chemistry</topic><topic>Humans</topic><topic>Immunohistochemistry - methods</topic><topic>Materials Testing</topic><topic>Microscopy, Electron, Transmission - methods</topic><topic>microtensile bond strength</topic><topic>proteoglycans</topic><topic>Proteoglycans - chemistry</topic><topic>Resin Cements - chemistry</topic><topic>Stress, Mechanical</topic><topic>Tensile Strength</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mazzoni, Annalisa</creatorcontrib><creatorcontrib>Pashley, David H.</creatorcontrib><creatorcontrib>Ruggeri Jr, Alessandra</creatorcontrib><creatorcontrib>Vita, Francesca</creatorcontrib><creatorcontrib>Falconi, Mirella</creatorcontrib><creatorcontrib>Di Lenarda, Roberto</creatorcontrib><creatorcontrib>Breschi, Lorenzo</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering 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>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</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>Mazzoni, Annalisa</au><au>Pashley, David H.</au><au>Ruggeri Jr, Alessandra</au><au>Vita, Francesca</au><au>Falconi, Mirella</au><au>Di Lenarda, Roberto</au><au>Breschi, Lorenzo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adhesion to chondroitinase ABC treated dentin</atitle><jtitle>Journal of biomedical materials research. Part B, Applied biomaterials</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>2008-07</date><risdate>2008</risdate><volume>86B</volume><issue>1</issue><spage>228</spage><epage>236</epage><pages>228-236</pages><issn>1552-4973</issn><eissn>1552-4981</eissn><abstract>Dentin bonding relies on complete resin impregnation throughout the demineralised hydrophilic collagen mesh. Chondroitin sulphate‐glycosaminoglycans are claimed to regulate the three‐dimensional arrangement of the dentin organic matrix and its hydrophilicity. The aim of this study was to investigate bond strength of two etch‐and‐rinse adhesives to chondroitinase ABC treated dentin. Human extracted molars were treated with chondroitinase ABC and a double labeling immunohistochemical technique was applied to reveal type I collagen and chondroitin 4/6 sulphate distribution under field emission in‐lens scanning electron microscope. The immunohistochemical technique confirmed the effective removal of chondroitin 4/6 sulphate after the enzymatic treatment. Dentin surfaces exposed to chondroitinase ABC and untreated specimens prepared on untreated acid‐etched dentin were bonded with Adper Scotchbond Multi‐Purpose or Prime and Bond NT. Bonded specimens were submitted to microtensile testing and nanoleakage interfacial analysis under transmission electron microscope. Increased mean values of microtensile bond strength and reduced nanoleakage expression were found for both adhesives after chondroitinase ABC treatment of the dentin surface. Adper Scotchbond Multi‐Purpose increased its bond strength about 28%, while bonding made with Prime and Bond NT almost doubled (92% increase) compared to untreated specimens. This study supports the hypothesis that adhesion can be enhanced by removal of chondroitin 4/6 sulphate and dermatan sulphate, probably due to a reduced amount of water content and enlarged interfibrillar spaces. Further studies should validate this hypothesis investigating the stability of chondroitin 4/6 and dermatan sulphate‐depleted dentin bonded interface over time. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>18161809</pmid><doi>10.1002/jbm.b.31010</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acid Etching, Dental - methods Chondroitin ABC Lyase - chemistry Dental Bonding - methods dental bonding systems dentin Dentin - chemistry Dentin-Bonding Agents - chemistry Dermatan Sulfate - chemistry Humans Immunohistochemistry - methods Materials Testing Microscopy, Electron, Transmission - methods microtensile bond strength proteoglycans Proteoglycans - chemistry Resin Cements - chemistry Stress, Mechanical Tensile Strength Water - chemistry |
title | Adhesion to chondroitinase ABC treated dentin |
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