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
Hauptverfasser: Lyle, Daniel B., Bushar, Grace S., Langone, John J.
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Langone, John J.
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
doi_str_mv 10.1002/jbm.a.32281
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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. 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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 &amp; 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. 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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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