Screening biomaterials for functional complement activation in serum
Complement plays an important role in the immune attack against invading microorganisms. However, blood‐contacting medical device biomaterials lacking specific complement inhibitors, with free hydroxyl and/or amino groups, or with absorbed antibodies, may inappropriately activate complement. Inappro...
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Veröffentlicht in: | Journal of biomedical materials research. Part A 2010-01, Vol.92A (1), p.205-213 |
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description | Complement plays an important role in the immune attack against invading microorganisms. However, blood‐contacting medical device biomaterials lacking specific complement inhibitors, with free hydroxyl and/or amino groups, or with absorbed antibodies, may inappropriately activate complement. Inappropriate activation by either the antibody‐mediated classical or the antibody‐independent alternative pathway may have well‐known acute or poorly understood chronic effects on the host or device. This article describes methods for screening biomaterials for functional whole complement activation using normal human serum, or specifically for alternative pathway activation using C4‐deficient guinea pig serum, or for classical pathway activation using both sera in combination. Detailed protocols are available as standard methodologies from the American Society for Testing and Materials (ASTM F1984, ASTM F2065, and ASTM F2567). Results obtained with these functional tests are confirmed by detection of classical and alternative pathway‐specific markers C4d and Bb, respectively. These methods demonstrate dose and time‐course activation of complement to beaded agarose, cellulose acetate, and purified alginate as examples of biomaterials. Significant difference in a functional endpoint denoting specific complement pathways is an appropriate screening method for complement activation by medical device biomaterials which might result in adverse events when the device is implanted or contacts human blood. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010 |
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However, blood‐contacting medical device biomaterials lacking specific complement inhibitors, with free hydroxyl and/or amino groups, or with absorbed antibodies, may inappropriately activate complement. Inappropriate activation by either the antibody‐mediated classical or the antibody‐independent alternative pathway may have well‐known acute or poorly understood chronic effects on the host or device. This article describes methods for screening biomaterials for functional whole complement activation using normal human serum, or specifically for alternative pathway activation using C4‐deficient guinea pig serum, or for classical pathway activation using both sera in combination. Detailed protocols are available as standard methodologies from the American Society for Testing and Materials (ASTM F1984, ASTM F2065, and ASTM F2567). Results obtained with these functional tests are confirmed by detection of classical and alternative pathway‐specific markers C4d and Bb, respectively. These methods demonstrate dose and time‐course activation of complement to beaded agarose, cellulose acetate, and purified alginate as examples of biomaterials. Significant difference in a functional endpoint denoting specific complement pathways is an appropriate screening method for complement activation by medical device biomaterials which might result in adverse events when the device is implanted or contacts human blood. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010</description><identifier>ISSN: 1549-3296</identifier><identifier>ISSN: 1552-4965</identifier><identifier>EISSN: 1552-4965</identifier><identifier>DOI: 10.1002/jbm.a.32281</identifier><identifier>PMID: 19172622</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Acetic acid ; Alginates ; Alginates - pharmacology ; Alginic acid ; Alternative pathway ; Amino groups ; Animals ; Antibodies ; Biocompatible Materials - pharmacology ; Biological and medical sciences ; Biomaterials ; Biomedical materials ; Blood ; Cellulose - analogs & derivatives ; Cellulose - pharmacology ; Cellulose acetate ; Chronic effects ; Classical pathway ; Complement ; Complement activation ; Complement Activation - drug effects ; Complement C4b - immunology ; Complement Factor B - immunology ; Complement inhibitors ; Complement Pathway, Alternative - drug effects ; Functional testing ; Glucuronic Acid - pharmacology ; Guinea Pigs ; Hemolysis - drug effects ; Hexuronic Acids - pharmacology ; Humans ; Materials Testing ; Medical devices ; Medical equipment ; Medical sciences ; Microorganisms ; Peptide Fragments - immunology ; Rabbits ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; screening ; Sepharose - pharmacology ; Serum - drug effects ; Serum - immunology ; Surgical implants ; Technology. Biomaterials. Equipments. Material. Instrumentation ; Time Factors ; Zymosan - pharmacology</subject><ispartof>Journal of biomedical materials research. Part A, 2010-01, Vol.92A (1), p.205-213</ispartof><rights>Copyright © 2009 Wiley Periodicals, Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright Wiley Subscription Services, Inc. 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Part A</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Complement plays an important role in the immune attack against invading microorganisms. However, blood‐contacting medical device biomaterials lacking specific complement inhibitors, with free hydroxyl and/or amino groups, or with absorbed antibodies, may inappropriately activate complement. Inappropriate activation by either the antibody‐mediated classical or the antibody‐independent alternative pathway may have well‐known acute or poorly understood chronic effects on the host or device. This article describes methods for screening biomaterials for functional whole complement activation using normal human serum, or specifically for alternative pathway activation using C4‐deficient guinea pig serum, or for classical pathway activation using both sera in combination. Detailed protocols are available as standard methodologies from the American Society for Testing and Materials (ASTM F1984, ASTM F2065, and ASTM F2567). Results obtained with these functional tests are confirmed by detection of classical and alternative pathway‐specific markers C4d and Bb, respectively. These methods demonstrate dose and time‐course activation of complement to beaded agarose, cellulose acetate, and purified alginate as examples of biomaterials. Significant difference in a functional endpoint denoting specific complement pathways is an appropriate screening method for complement activation by medical device biomaterials which might result in adverse events when the device is implanted or contacts human blood. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010</description><subject>Acetic acid</subject><subject>Alginates</subject><subject>Alginates - pharmacology</subject><subject>Alginic acid</subject><subject>Alternative pathway</subject><subject>Amino groups</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Biocompatible Materials - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Biomaterials</subject><subject>Biomedical materials</subject><subject>Blood</subject><subject>Cellulose - analogs & derivatives</subject><subject>Cellulose - pharmacology</subject><subject>Cellulose acetate</subject><subject>Chronic effects</subject><subject>Classical pathway</subject><subject>Complement</subject><subject>Complement activation</subject><subject>Complement Activation - drug effects</subject><subject>Complement C4b - immunology</subject><subject>Complement Factor B - immunology</subject><subject>Complement inhibitors</subject><subject>Complement Pathway, Alternative - drug effects</subject><subject>Functional testing</subject><subject>Glucuronic Acid - pharmacology</subject><subject>Guinea Pigs</subject><subject>Hemolysis - drug effects</subject><subject>Hexuronic Acids - pharmacology</subject><subject>Humans</subject><subject>Materials Testing</subject><subject>Medical devices</subject><subject>Medical equipment</subject><subject>Medical sciences</subject><subject>Microorganisms</subject><subject>Peptide Fragments - immunology</subject><subject>Rabbits</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>screening</subject><subject>Sepharose - pharmacology</subject><subject>Serum - drug effects</subject><subject>Serum - immunology</subject><subject>Surgical implants</subject><subject>Technology. Biomaterials. Equipments. Material. Instrumentation</subject><subject>Time Factors</subject><subject>Zymosan - pharmacology</subject><issn>1549-3296</issn><issn>1552-4965</issn><issn>1552-4965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0Utv1DAQAGALgegDTtxRJFRxQFnsiR_xkRZoqRY4UMrRcpwx8pLHYieF_nu83W2ROFDJkq3xNzOyh5BnjC4YpfB61fQLu6gAavaA7DMhoORaioebM9dlBVrukYOUVhlLKuAx2WOaKZAA--TtFxcRhzB8L5ow9nbCGGyXCj_Gws-Dm8I42K5wY7_usMdhKmyOXdlNvAhDkTDO_RPyyOckfLrbD8nX9-8uTs7K5efTDydvlqXjmrKyZZ7ZytXUo9IOPHecomBeSIWS-qaBxtmaI4Paaa6UV630sqV1vmzzqg7Jy23ddRx_zpgm04fksOvsgOOcTF1XFIBydr-UWijOtLxXqoozAZpDli_-katxjvl3kgFdKcFqLnlWr7bKxTGliN6sY-htvDaMms28TJ6XseZmXlk_39Wcmx7bv3Y3oAyOdsAmZzsf7eBCunMAnAp-82C2db9Ch9f_62nOjz_eNi-3OSFN-Psux8YfRqr8IPPt06m5rJfAxOWFOav-AHg4uzY</recordid><startdate>201001</startdate><enddate>201001</enddate><creator>Lyle, Daniel B.</creator><creator>Bushar, Grace S.</creator><creator>Langone, John J.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</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>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</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></search><sort><creationdate>201001</creationdate><title>Screening biomaterials for functional complement activation in serum</title><author>Lyle, Daniel B. ; Bushar, Grace S. ; Langone, John J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4901-d1f1a3c80fe79c2f4c40e51f567e60fbb2bca84e128c9477f7d6f6d0860fd0fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acetic acid</topic><topic>Alginates</topic><topic>Alginates - pharmacology</topic><topic>Alginic acid</topic><topic>Alternative pathway</topic><topic>Amino groups</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Biocompatible Materials - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Biomaterials</topic><topic>Biomedical materials</topic><topic>Blood</topic><topic>Cellulose - analogs & derivatives</topic><topic>Cellulose - pharmacology</topic><topic>Cellulose acetate</topic><topic>Chronic effects</topic><topic>Classical pathway</topic><topic>Complement</topic><topic>Complement activation</topic><topic>Complement Activation - drug effects</topic><topic>Complement C4b - immunology</topic><topic>Complement Factor B - immunology</topic><topic>Complement inhibitors</topic><topic>Complement Pathway, Alternative - drug effects</topic><topic>Functional testing</topic><topic>Glucuronic Acid - pharmacology</topic><topic>Guinea Pigs</topic><topic>Hemolysis - drug effects</topic><topic>Hexuronic Acids - pharmacology</topic><topic>Humans</topic><topic>Materials Testing</topic><topic>Medical devices</topic><topic>Medical equipment</topic><topic>Medical sciences</topic><topic>Microorganisms</topic><topic>Peptide Fragments - immunology</topic><topic>Rabbits</topic><topic>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</topic><topic>screening</topic><topic>Sepharose - pharmacology</topic><topic>Serum - drug effects</topic><topic>Serum - immunology</topic><topic>Surgical implants</topic><topic>Technology. Biomaterials. Equipments. Material. Instrumentation</topic><topic>Time Factors</topic><topic>Zymosan - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lyle, Daniel B.</creatorcontrib><creatorcontrib>Bushar, Grace S.</creatorcontrib><creatorcontrib>Langone, John J.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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>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>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 A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lyle, Daniel B.</au><au>Bushar, Grace S.</au><au>Langone, John J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Screening biomaterials for functional complement activation in serum</atitle><jtitle>Journal of biomedical materials research. Part A</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>2010-01</date><risdate>2010</risdate><volume>92A</volume><issue>1</issue><spage>205</spage><epage>213</epage><pages>205-213</pages><issn>1549-3296</issn><issn>1552-4965</issn><eissn>1552-4965</eissn><abstract>Complement plays an important role in the immune attack against invading microorganisms. However, blood‐contacting medical device biomaterials lacking specific complement inhibitors, with free hydroxyl and/or amino groups, or with absorbed antibodies, may inappropriately activate complement. Inappropriate activation by either the antibody‐mediated classical or the antibody‐independent alternative pathway may have well‐known acute or poorly understood chronic effects on the host or device. This article describes methods for screening biomaterials for functional whole complement activation using normal human serum, or specifically for alternative pathway activation using C4‐deficient guinea pig serum, or for classical pathway activation using both sera in combination. Detailed protocols are available as standard methodologies from the American Society for Testing and Materials (ASTM F1984, ASTM F2065, and ASTM F2567). Results obtained with these functional tests are confirmed by detection of classical and alternative pathway‐specific markers C4d and Bb, respectively. These methods demonstrate dose and time‐course activation of complement to beaded agarose, cellulose acetate, and purified alginate as examples of biomaterials. Significant difference in a functional endpoint denoting specific complement pathways is an appropriate screening method for complement activation by medical device biomaterials which might result in adverse events when the device is implanted or contacts human blood. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19172622</pmid><doi>10.1002/jbm.a.32281</doi><tpages>9</tpages></addata></record> |
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subjects | Acetic acid Alginates Alginates - pharmacology Alginic acid Alternative pathway Amino groups Animals Antibodies Biocompatible Materials - pharmacology Biological and medical sciences Biomaterials Biomedical materials Blood Cellulose - analogs & derivatives Cellulose - pharmacology Cellulose acetate Chronic effects Classical pathway Complement Complement activation Complement Activation - drug effects Complement C4b - immunology Complement Factor B - immunology Complement inhibitors Complement Pathway, Alternative - drug effects Functional testing Glucuronic Acid - pharmacology Guinea Pigs Hemolysis - drug effects Hexuronic Acids - pharmacology Humans Materials Testing Medical devices Medical equipment Medical sciences Microorganisms Peptide Fragments - immunology Rabbits Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) screening Sepharose - pharmacology Serum - drug effects Serum - immunology Surgical implants Technology. Biomaterials. Equipments. Material. Instrumentation Time Factors Zymosan - pharmacology |
title | Screening biomaterials for functional complement activation in serum |
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