Grafting of architecture controlled poly(styrene sodium sulfonate) onto titanium surfaces using bio-adhesive molecules: Surface characterization and biological properties.
Identifieur interne : 000B34 ( PubMed/Checkpoint ); précédent : 000B33; suivant : 000B35Grafting of architecture controlled poly(styrene sodium sulfonate) onto titanium surfaces using bio-adhesive molecules: Surface characterization and biological properties.
Auteurs : Hamza Chouirfa [France] ; Margaret D M. Evans [Australie] ; David G. Castner [États-Unis] ; Penny Bean [Australie] ; Dimitri Mercier [France] ; Anouk Galtayries [France] ; Céline Falentin-Daudré [France] ; Véronique Migonney [France]Source :
- Biointerphases [ 1559-4106 ] ; 2017.
Abstract
This contribution reports on grafting of bioactive polymers such as poly(sodium styrene sulfonate) (polyNaSS) onto titanium (Ti) surfaces. This grafting process uses a modified dopamine as an anchor molecule to link polyNaSS to the Ti surface. The grafting process combines reversible addition-fragmentation chain transfer polymerization, postpolymerization modification, and thiol-ene chemistry. The first step in the process is to synthetize architecture controlled polyNaSS with a thiol end group. The second step is the adhesion of the dopamine acrylamide (DA) anchor onto the Ti surfaces. The last step is grafting polyNaSS to the DA-modified Ti surfaces. The modified dopamine anchor group with its bioadhesive properties is essential to link bioactive polymers to the Ti surface. The polymers are characterized by conventional methods (nuclear magnetic resonance, size exclusion chromatography, and attenuated total reflection-Fourier-transformed infrared), and the grafting is characterized by x-ray photoelectron spectroscopy, time-of-flight secondary ion mass spectrometry, and quartz crystal microbalance with dissipation monitoring. To illustrate the biocompatibility of the grafted Ti-DA-polyNaSS surfaces, their interactions with proteins (albumin and fibronectin) and cells are investigated. Both albumin and fibronectin are readily adsorbed onto Ti-DA-polyNaSS surfaces. The biocompatibility of modified Ti-DA-polyNaSS and control ungrafted Ti surfaces is tested using human bone cells (Saos-2) in cell culture for cell adhesion, proliferation, differentiation, and mineralization. This study presents a new, simple way to graft bioactive polymers onto Ti surfaces using a catechol intermediary with the aim of demonstrating the biocompatibility of these size controlled polyNaSS grafted surfaces.
DOI: 10.1116/1.4985608
PubMed: 28614950
Affiliations:
- Australie, France, États-Unis
- Washington (État), Île-de-France
- Paris, Villetaneuse
- Université Paris 13
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properties.</title><author><name sortKey="Chouirfa, Hamza" sort="Chouirfa, Hamza" uniqKey="Chouirfa H" first="Hamza" last="Chouirfa">Hamza Chouirfa</name><affiliation wicri:level="4"><nlm:affiliation>LBPS/CSPBAT, UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 Avenue JB Clément, 93340 Villetaneuse, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>LBPS/CSPBAT, UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 Avenue JB Clément, 93340 Villetaneuse</wicri:regionArea><placeName><region type="region" nuts="2">Île-de-France</region><settlement type="city">Villetaneuse</settlement><settlement type="city">Paris</settlement></placeName><orgName type="university">Université Paris 13</orgName></affiliation></author><author><name sortKey="Evans, Margaret D M" sort="Evans, Margaret D M" uniqKey="Evans M" first="Margaret D M" last="Evans">Margaret D M. Evans</name><affiliation wicri:level="1"><nlm:affiliation>CSIRO Biomedical Materials Manufacturing Program, 11 Julius Avenue, North Ryde, Sydney, NSW 2113, Australia.</nlm:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>CSIRO Biomedical Materials Manufacturing Program, 11 Julius Avenue, North Ryde, Sydney, NSW 2113</wicri:regionArea><wicri:noRegion>NSW 2113</wicri:noRegion></affiliation></author><author><name sortKey="Castner, David G" sort="Castner, David G" uniqKey="Castner D" first="David G" last="Castner">David G. Castner</name><affiliation wicri:level="2"><nlm:affiliation>National ESCA and Surface Analysis Center for Biomedical Problems, Departments of Bioengineering and Chemical Engineering, University of Washington, Seattle, Washington 98195-1653.</nlm:affiliation><country xml:lang="fr">États-Unis</country><placeName><region type="state">Washington (État)</region></placeName><wicri:cityArea>National ESCA and Surface Analysis Center for Biomedical Problems, Departments of Bioengineering and Chemical Engineering, University of Washington, Seattle</wicri:cityArea></affiliation></author><author><name sortKey="Bean, Penny" sort="Bean, Penny" uniqKey="Bean P" first="Penny" last="Bean">Penny Bean</name><affiliation wicri:level="1"><nlm:affiliation>CSIRO Biomedical Materials Manufacturing Program, 11 Julius Avenue, North Ryde, Sydney, NSW 2113, Australia.</nlm:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>CSIRO Biomedical Materials Manufacturing Program, 11 Julius Avenue, North Ryde, Sydney, NSW 2113</wicri:regionArea><wicri:noRegion>NSW 2113</wicri:noRegion></affiliation></author><author><name sortKey="Mercier, Dimitri" sort="Mercier, Dimitri" uniqKey="Mercier D" first="Dimitri" last="Mercier">Dimitri Mercier</name><affiliation wicri:level="1"><nlm:affiliation>PSL Research University, Chimie ParisTech-CNRS, Institut de Recherche de Chimie Paris, 75005 Paris, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>PSL Research University, Chimie ParisTech-CNRS, Institut de Recherche de Chimie Paris, 75005 Paris</wicri:regionArea><wicri:noRegion>75005 Paris</wicri:noRegion><placeName><settlement type="city">Paris</settlement><region type="région" nuts="2">Île-de-France</region></placeName></affiliation></author><author><name sortKey="Galtayries, Anouk" sort="Galtayries, Anouk" uniqKey="Galtayries A" first="Anouk" last="Galtayries">Anouk Galtayries</name><affiliation wicri:level="1"><nlm:affiliation>PSL Research University, Chimie ParisTech-CNRS, Institut de Recherche de Chimie Paris, 75005 Paris, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>PSL Research University, Chimie ParisTech-CNRS, Institut de Recherche de Chimie Paris, 75005 Paris</wicri:regionArea><wicri:noRegion>75005 Paris</wicri:noRegion><placeName><settlement type="city">Paris</settlement><region type="région" nuts="2">Île-de-France</region></placeName></affiliation></author><author><name sortKey="Falentin Daudre, Celine" sort="Falentin Daudre, Celine" uniqKey="Falentin Daudre C" first="Céline" last="Falentin-Daudré">Céline Falentin-Daudré</name><affiliation wicri:level="4"><nlm:affiliation>LBPS/CSPBAT, UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 Avenue JB Clément, 93340 Villetaneuse, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>LBPS/CSPBAT, UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 Avenue JB Clément, 93340 Villetaneuse</wicri:regionArea><wicri:noRegion>93340 Villetaneuse</wicri:noRegion><orgName type="university">Université Paris 13</orgName><placeName><settlement type="city">Paris</settlement><region type="region" nuts="2">Île-de-France</region></placeName></affiliation></author><author><name sortKey="Migonney, Veronique" sort="Migonney, Veronique" uniqKey="Migonney V" first="Véronique" last="Migonney">Véronique Migonney</name><affiliation wicri:level="4"><nlm:affiliation>LBPS/CSPBAT, UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 Avenue JB Clément, 93340 Villetaneuse, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>LBPS/CSPBAT, UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 Avenue JB Clément, 93340 Villetaneuse</wicri:regionArea><wicri:noRegion>93340 Villetaneuse</wicri:noRegion><orgName type="university">Université Paris 13</orgName><placeName><settlement type="city">Paris</settlement><region type="region" nuts="2">Île-de-France</region></placeName></affiliation></author></analytic><series><title level="j">Biointerphases</title><idno type="eISSN">1559-4106</idno><imprint><date when="2017" type="published">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">This contribution reports on grafting of bioactive polymers such as poly(sodium styrene sulfonate) (polyNaSS) onto titanium (Ti) surfaces. This grafting process uses a modified dopamine as an anchor molecule to link polyNaSS to the Ti surface. The grafting process combines reversible addition-fragmentation chain transfer polymerization, postpolymerization modification, and thiol-ene chemistry. The first step in the process is to synthetize architecture controlled polyNaSS with a thiol end group. The second step is the adhesion of the dopamine acrylamide (DA) anchor onto the Ti surfaces. The last step is grafting polyNaSS to the DA-modified Ti surfaces. The modified dopamine anchor group with its bioadhesive properties is essential to link bioactive polymers to the Ti surface. The polymers are characterized by conventional methods (nuclear magnetic resonance, size exclusion chromatography, and attenuated total reflection-Fourier-transformed infrared), and the grafting is characterized by x-ray photoelectron spectroscopy, time-of-flight secondary ion mass spectrometry, and quartz crystal microbalance with dissipation monitoring. To illustrate the biocompatibility of the grafted Ti-DA-polyNaSS surfaces, their interactions with proteins (albumin and fibronectin) and cells are investigated. Both albumin and fibronectin are readily adsorbed onto Ti-DA-polyNaSS surfaces. The biocompatibility of modified Ti-DA-polyNaSS and control ungrafted Ti surfaces is tested using human bone cells (Saos-2) in cell culture for cell adhesion, proliferation, differentiation, and mineralization. This study presents a new, simple way to graft bioactive polymers onto Ti surfaces using a catechol intermediary with the aim of demonstrating the biocompatibility of these size controlled polyNaSS grafted surfaces.</div></front></TEI><pubmed><MedlineCitation Status="In-Process" Owner="NLM"><PMID Version="1">28614950</PMID><DateCreated><Year>2017</Year><Month>06</Month><Day>15</Day></DateCreated><DateRevised><Year>2017</Year><Month>09</Month><Day>19</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1559-4106</ISSN><JournalIssue CitedMedium="Internet"><Volume>12</Volume><Issue>2</Issue><PubDate><Year>2017</Year><Month>Jun</Month><Day>14</Day></PubDate></JournalIssue><Title>Biointerphases</Title><ISOAbbreviation>Biointerphases</ISOAbbreviation></Journal><ArticleTitle>Grafting of architecture controlled poly(styrene sodium sulfonate) onto titanium surfaces using bio-adhesive molecules: Surface characterization and biological properties.</ArticleTitle><Pagination><MedlinePgn>02C418</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1116/1.4985608</ELocationID><Abstract><AbstractText>This contribution reports on grafting of bioactive polymers such as poly(sodium styrene sulfonate) (polyNaSS) onto titanium (Ti) surfaces. This grafting process uses a modified dopamine as an anchor molecule to link polyNaSS to the Ti surface. The grafting process combines reversible addition-fragmentation chain transfer polymerization, postpolymerization modification, and thiol-ene chemistry. The first step in the process is to synthetize architecture controlled polyNaSS with a thiol end group. The second step is the adhesion of the dopamine acrylamide (DA) anchor onto the Ti surfaces. The last step is grafting polyNaSS to the DA-modified Ti surfaces. The modified dopamine anchor group with its bioadhesive properties is essential to link bioactive polymers to the Ti surface. The polymers are characterized by conventional methods (nuclear magnetic resonance, size exclusion chromatography, and attenuated total reflection-Fourier-transformed infrared), and the grafting is characterized by x-ray photoelectron spectroscopy, time-of-flight secondary ion mass spectrometry, and quartz crystal microbalance with dissipation monitoring. To illustrate the biocompatibility of the grafted Ti-DA-polyNaSS surfaces, their interactions with proteins (albumin and fibronectin) and cells are investigated. Both albumin and fibronectin are readily adsorbed onto Ti-DA-polyNaSS surfaces. The biocompatibility of modified Ti-DA-polyNaSS and control ungrafted Ti surfaces is tested using human bone cells (Saos-2) in cell culture for cell adhesion, proliferation, differentiation, and mineralization. This study presents a new, simple way to graft bioactive polymers onto Ti surfaces using a catechol intermediary with the aim of demonstrating the biocompatibility of these size controlled polyNaSS grafted surfaces.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Chouirfa</LastName><ForeName>Hamza</ForeName><Initials>H</Initials><AffiliationInfo><Affiliation>LBPS/CSPBAT, UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 Avenue JB Clément, 93340 Villetaneuse, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Evans</LastName><ForeName>Margaret D M</ForeName><Initials>MDM</Initials><AffiliationInfo><Affiliation>CSIRO Biomedical Materials Manufacturing Program, 11 Julius Avenue, North Ryde, Sydney, NSW 2113, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Castner</LastName><ForeName>David G</ForeName><Initials>DG</Initials><AffiliationInfo><Affiliation>National ESCA and Surface Analysis Center for Biomedical Problems, Departments of Bioengineering and Chemical Engineering, University of Washington, Seattle, Washington 98195-1653.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Bean</LastName><ForeName>Penny</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>CSIRO Biomedical Materials Manufacturing Program, 11 Julius Avenue, North Ryde, Sydney, NSW 2113, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Mercier</LastName><ForeName>Dimitri</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>PSL Research University, Chimie ParisTech-CNRS, Institut de Recherche de Chimie Paris, 75005 Paris, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Galtayries</LastName><ForeName>Anouk</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>PSL Research University, Chimie ParisTech-CNRS, Institut de Recherche de Chimie Paris, 75005 Paris, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Falentin-Daudré</LastName><ForeName>Céline</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>LBPS/CSPBAT, UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 Avenue JB Clément, 93340 Villetaneuse, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Migonney</LastName><ForeName>Véronique</ForeName><Initials>V</Initials><AffiliationInfo><Affiliation>LBPS/CSPBAT, UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 Avenue JB Clément, 93340 Villetaneuse, France.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>P41 EB002027</GrantID><Acronym>EB</Acronym><Agency>NIBIB NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate 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IdType="pmc">PMC5599117</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Australie</li><li>France</li><li>États-Unis</li></country><region><li>Washington (État)</li><li>Île-de-France</li></region><settlement><li>Paris</li><li>Villetaneuse</li></settlement><orgName><li>Université Paris 13</li></orgName></list><tree><country name="France"><region name="Île-de-France"><name sortKey="Chouirfa, Hamza" sort="Chouirfa, Hamza" uniqKey="Chouirfa H" first="Hamza" last="Chouirfa">Hamza Chouirfa</name></region><name sortKey="Falentin Daudre, Celine" sort="Falentin Daudre, Celine" uniqKey="Falentin Daudre C" first="Céline" last="Falentin-Daudré">Céline Falentin-Daudré</name><name sortKey="Galtayries, Anouk" sort="Galtayries, Anouk" uniqKey="Galtayries A" first="Anouk" last="Galtayries">Anouk Galtayries</name><name sortKey="Mercier, Dimitri" sort="Mercier, Dimitri" uniqKey="Mercier D" first="Dimitri" last="Mercier">Dimitri Mercier</name><name sortKey="Migonney, Veronique" sort="Migonney, Veronique" uniqKey="Migonney V" first="Véronique" last="Migonney">Véronique Migonney</name></country><country name="Australie"><noRegion><name sortKey="Evans, Margaret D M" sort="Evans, Margaret D M" uniqKey="Evans M" first="Margaret D M" last="Evans">Margaret D M. Evans</name></noRegion><name sortKey="Bean, Penny" sort="Bean, Penny" uniqKey="Bean P" first="Penny" last="Bean">Penny Bean</name></country><country name="États-Unis"><region name="Washington (État)"><name sortKey="Castner, David G" sort="Castner, David G" uniqKey="Castner D" first="David G" last="Castner">David G. Castner</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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