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Highly Hydrophilic Surfaces from Polyglycidol Grafts with Dual Antifouling and Specific Protein Recognition Properties
Homopolymer grafts from α-tert-butoxy-ω-vinylbenzyl-polyglycidol (PGL) were prepared on gold and stainless steel (SS) substrates modified by 4-benzoyl-phenyl (BP) moieties derived from the electroreduction of the parent salt 4-benzoyl benzene diazonium tetrafluoroborate. The grafted BP aryl groups e...
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Published in: | Langmuir 2011-08, Vol.27 (15), p.9285-9294 |
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creator | Gam-Derouich, Sarra Gosecka, Monika Lepinay, Sandrine Turmine, Mireille Carbonnier, Benjamin Basinska, Teresa Slomkowski, Stanislaw Millot, Marie-Claude Othmane, Ali Ben Hassen-Chehimi, Dalila Chehimi, Mohamed M |
description | Homopolymer grafts from α-tert-butoxy-ω-vinylbenzyl-polyglycidol (PGL) were prepared on gold and stainless steel (SS) substrates modified by 4-benzoyl-phenyl (BP) moieties derived from the electroreduction of the parent salt 4-benzoyl benzene diazonium tetrafluoroborate. The grafted BP aryl groups efficiently served to surface-initiate photopolymerization (SIPP) of PGL. In similar conditions, SIPP of hydroxyethyl methacrylate (HEMA) permitted the production of PHEMA grafts as model surfaces. Water contact angles were found to be 66°, 15°, and 0° for SS-BP, SS-PHEMA, and SS-PPGL, respectively. The spontaneous spreading of water drops on SS-PPGL was invariably observed with 1.5 μL water drops. PPGL thus appears as a superhydrophilic polymer. Resistance to nonspecific adsorption of proteins of PPGL and PHEMA grafts on gold was evaluated by surface plasmon resonance (SPR) using antibovine serum albumin (anti-BSA). The results conclusively show that PPGL-grafts exhibit enhanced resistance to anti-BSA adsorption compared to the well-known hydrophilic PHEMA. PPGL grafts were further modified with BSA through the carbonyldiimidazole activation of the OH groups providing immunosensing surfaces. The so-prepared PPGL-grafted BSA hybrids specifically interacted with anti-BSA in PBS as compared to antimyoglobin. It is clear that the superhydrophilic character of PPGL grafts opens new avenues for biomedical applications where surfaces with dual functionality, namely, specific protein grafting together with resistance to biofouling, are required. |
doi_str_mv | 10.1021/la200290k |
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The grafted BP aryl groups efficiently served to surface-initiate photopolymerization (SIPP) of PGL. In similar conditions, SIPP of hydroxyethyl methacrylate (HEMA) permitted the production of PHEMA grafts as model surfaces. Water contact angles were found to be 66°, 15°, and 0° for SS-BP, SS-PHEMA, and SS-PPGL, respectively. The spontaneous spreading of water drops on SS-PPGL was invariably observed with 1.5 μL water drops. PPGL thus appears as a superhydrophilic polymer. Resistance to nonspecific adsorption of proteins of PPGL and PHEMA grafts on gold was evaluated by surface plasmon resonance (SPR) using antibovine serum albumin (anti-BSA). The results conclusively show that PPGL-grafts exhibit enhanced resistance to anti-BSA adsorption compared to the well-known hydrophilic PHEMA. PPGL grafts were further modified with BSA through the carbonyldiimidazole activation of the OH groups providing immunosensing surfaces. The so-prepared PPGL-grafted BSA hybrids specifically interacted with anti-BSA in PBS as compared to antimyoglobin. It is clear that the superhydrophilic character of PPGL grafts opens new avenues for biomedical applications where surfaces with dual functionality, namely, specific protein grafting together with resistance to biofouling, are required.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/la200290k</identifier><identifier>PMID: 21678957</identifier><identifier>CODEN: LANGD5</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Adsorption ; Animals ; Biofouling - prevention & control ; Cattle ; Chemical Sciences ; Chemistry ; Exact sciences and technology ; General and physical chemistry ; Gold - chemistry ; Interfaces: Adsorption, Reactions, Films, Forces ; Molecular Structure ; Other ; Particle Size ; Propylene Glycols - chemical synthesis ; Propylene Glycols - chemistry ; Serum Albumin, Bovine - chemistry ; Solid-liquid interface ; Stainless Steel - chemistry ; Surface physical chemistry ; Surface Properties</subject><ispartof>Langmuir, 2011-08, Vol.27 (15), p.9285-9294</ispartof><rights>Copyright © 2011 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a338t-5c7dbe337e275d28045393619ce5c1e7d66e724395f55ff44a5dada864fbbf683</cites><orcidid>0000-0002-6098-983X ; 0000-0002-5939-5065 ; 0000-0001-8358-9903 ; 0000-0001-6844-3762</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24387486$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21678957$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.sorbonne-universite.fr/hal-00829961$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Gam-Derouich, Sarra</creatorcontrib><creatorcontrib>Gosecka, Monika</creatorcontrib><creatorcontrib>Lepinay, Sandrine</creatorcontrib><creatorcontrib>Turmine, Mireille</creatorcontrib><creatorcontrib>Carbonnier, Benjamin</creatorcontrib><creatorcontrib>Basinska, Teresa</creatorcontrib><creatorcontrib>Slomkowski, Stanislaw</creatorcontrib><creatorcontrib>Millot, Marie-Claude</creatorcontrib><creatorcontrib>Othmane, Ali</creatorcontrib><creatorcontrib>Ben Hassen-Chehimi, Dalila</creatorcontrib><creatorcontrib>Chehimi, Mohamed M</creatorcontrib><title>Highly Hydrophilic Surfaces from Polyglycidol Grafts with Dual Antifouling and Specific Protein Recognition Properties</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>Homopolymer grafts from α-tert-butoxy-ω-vinylbenzyl-polyglycidol (PGL) were prepared on gold and stainless steel (SS) substrates modified by 4-benzoyl-phenyl (BP) moieties derived from the electroreduction of the parent salt 4-benzoyl benzene diazonium tetrafluoroborate. The grafted BP aryl groups efficiently served to surface-initiate photopolymerization (SIPP) of PGL. In similar conditions, SIPP of hydroxyethyl methacrylate (HEMA) permitted the production of PHEMA grafts as model surfaces. Water contact angles were found to be 66°, 15°, and 0° for SS-BP, SS-PHEMA, and SS-PPGL, respectively. The spontaneous spreading of water drops on SS-PPGL was invariably observed with 1.5 μL water drops. PPGL thus appears as a superhydrophilic polymer. Resistance to nonspecific adsorption of proteins of PPGL and PHEMA grafts on gold was evaluated by surface plasmon resonance (SPR) using antibovine serum albumin (anti-BSA). The results conclusively show that PPGL-grafts exhibit enhanced resistance to anti-BSA adsorption compared to the well-known hydrophilic PHEMA. PPGL grafts were further modified with BSA through the carbonyldiimidazole activation of the OH groups providing immunosensing surfaces. The so-prepared PPGL-grafted BSA hybrids specifically interacted with anti-BSA in PBS as compared to antimyoglobin. It is clear that the superhydrophilic character of PPGL grafts opens new avenues for biomedical applications where surfaces with dual functionality, namely, specific protein grafting together with resistance to biofouling, are required.</description><subject>Adsorption</subject><subject>Animals</subject><subject>Biofouling - prevention & control</subject><subject>Cattle</subject><subject>Chemical Sciences</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Gold - chemistry</subject><subject>Interfaces: Adsorption, Reactions, Films, Forces</subject><subject>Molecular Structure</subject><subject>Other</subject><subject>Particle Size</subject><subject>Propylene Glycols - chemical synthesis</subject><subject>Propylene Glycols - chemistry</subject><subject>Serum Albumin, Bovine - chemistry</subject><subject>Solid-liquid interface</subject><subject>Stainless Steel - chemistry</subject><subject>Surface physical chemistry</subject><subject>Surface Properties</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpt0ctuEzEUBmALgWgoLHgB5A1CXQz4fllGhTZIkagorEeOx05cHHuwZ4rm7ZmoIdmwOtLRp_9I5wfgLUYfMSL4UzQEIaLRr2dggTlBDVdEPgcLJBltJBP0Aryq9QEhpCnTL8EFwUIqzeUCPK7CdhcnuJq6kvtdiMHC-7F4Y12FvuQ9vMtx2sbJhi5HeFuMHyr8E4Yd_DyaCJdpCD6PMaQtNKmD972zwc8hdyUPLiT43dm8TWEIOR12vStDcPU1eOFNrO7NcV6CnzdfflyvmvW326_Xy3VjKFVDw63sNo5S6YjkHVGIcaqpwNo6brGTnRBOEkY195x7z5jhnemMEsxvNl4oegmunnJ3JrZ9CXtTpjab0K6W6_awQ0gRrQV-xLP98GT7kn-Prg7tPlTrYjTJ5bG2Smo2Y4bPqbbkWovzp2iM2kMj7amR2b47po6bvetO8l8FM3h_BKZaE30xyYZ6dowqyZQ4O2Nr-5DHkubH_efgX2qxn-c</recordid><startdate>20110802</startdate><enddate>20110802</enddate><creator>Gam-Derouich, Sarra</creator><creator>Gosecka, Monika</creator><creator>Lepinay, Sandrine</creator><creator>Turmine, Mireille</creator><creator>Carbonnier, Benjamin</creator><creator>Basinska, Teresa</creator><creator>Slomkowski, Stanislaw</creator><creator>Millot, Marie-Claude</creator><creator>Othmane, Ali</creator><creator>Ben Hassen-Chehimi, Dalila</creator><creator>Chehimi, Mohamed M</creator><general>American Chemical Society</general><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>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-6098-983X</orcidid><orcidid>https://orcid.org/0000-0002-5939-5065</orcidid><orcidid>https://orcid.org/0000-0001-8358-9903</orcidid><orcidid>https://orcid.org/0000-0001-6844-3762</orcidid></search><sort><creationdate>20110802</creationdate><title>Highly Hydrophilic Surfaces from Polyglycidol Grafts with Dual Antifouling and Specific Protein Recognition Properties</title><author>Gam-Derouich, Sarra ; Gosecka, Monika ; Lepinay, Sandrine ; Turmine, Mireille ; Carbonnier, Benjamin ; Basinska, Teresa ; Slomkowski, Stanislaw ; Millot, Marie-Claude ; Othmane, Ali ; Ben Hassen-Chehimi, Dalila ; Chehimi, Mohamed M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a338t-5c7dbe337e275d28045393619ce5c1e7d66e724395f55ff44a5dada864fbbf683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adsorption</topic><topic>Animals</topic><topic>Biofouling - prevention & control</topic><topic>Cattle</topic><topic>Chemical Sciences</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Gold - chemistry</topic><topic>Interfaces: Adsorption, Reactions, Films, Forces</topic><topic>Molecular Structure</topic><topic>Other</topic><topic>Particle Size</topic><topic>Propylene Glycols - chemical synthesis</topic><topic>Propylene Glycols - chemistry</topic><topic>Serum Albumin, Bovine - chemistry</topic><topic>Solid-liquid interface</topic><topic>Stainless Steel - chemistry</topic><topic>Surface physical chemistry</topic><topic>Surface Properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gam-Derouich, Sarra</creatorcontrib><creatorcontrib>Gosecka, Monika</creatorcontrib><creatorcontrib>Lepinay, Sandrine</creatorcontrib><creatorcontrib>Turmine, Mireille</creatorcontrib><creatorcontrib>Carbonnier, Benjamin</creatorcontrib><creatorcontrib>Basinska, Teresa</creatorcontrib><creatorcontrib>Slomkowski, Stanislaw</creatorcontrib><creatorcontrib>Millot, Marie-Claude</creatorcontrib><creatorcontrib>Othmane, Ali</creatorcontrib><creatorcontrib>Ben Hassen-Chehimi, Dalila</creatorcontrib><creatorcontrib>Chehimi, Mohamed M</creatorcontrib><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>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gam-Derouich, Sarra</au><au>Gosecka, Monika</au><au>Lepinay, Sandrine</au><au>Turmine, Mireille</au><au>Carbonnier, Benjamin</au><au>Basinska, Teresa</au><au>Slomkowski, Stanislaw</au><au>Millot, Marie-Claude</au><au>Othmane, Ali</au><au>Ben Hassen-Chehimi, Dalila</au><au>Chehimi, Mohamed M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly Hydrophilic Surfaces from Polyglycidol Grafts with Dual Antifouling and Specific Protein Recognition Properties</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2011-08-02</date><risdate>2011</risdate><volume>27</volume><issue>15</issue><spage>9285</spage><epage>9294</epage><pages>9285-9294</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>Homopolymer grafts from α-tert-butoxy-ω-vinylbenzyl-polyglycidol (PGL) were prepared on gold and stainless steel (SS) substrates modified by 4-benzoyl-phenyl (BP) moieties derived from the electroreduction of the parent salt 4-benzoyl benzene diazonium tetrafluoroborate. The grafted BP aryl groups efficiently served to surface-initiate photopolymerization (SIPP) of PGL. In similar conditions, SIPP of hydroxyethyl methacrylate (HEMA) permitted the production of PHEMA grafts as model surfaces. Water contact angles were found to be 66°, 15°, and 0° for SS-BP, SS-PHEMA, and SS-PPGL, respectively. The spontaneous spreading of water drops on SS-PPGL was invariably observed with 1.5 μL water drops. PPGL thus appears as a superhydrophilic polymer. Resistance to nonspecific adsorption of proteins of PPGL and PHEMA grafts on gold was evaluated by surface plasmon resonance (SPR) using antibovine serum albumin (anti-BSA). The results conclusively show that PPGL-grafts exhibit enhanced resistance to anti-BSA adsorption compared to the well-known hydrophilic PHEMA. PPGL grafts were further modified with BSA through the carbonyldiimidazole activation of the OH groups providing immunosensing surfaces. The so-prepared PPGL-grafted BSA hybrids specifically interacted with anti-BSA in PBS as compared to antimyoglobin. It is clear that the superhydrophilic character of PPGL grafts opens new avenues for biomedical applications where surfaces with dual functionality, namely, specific protein grafting together with resistance to biofouling, are required.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>21678957</pmid><doi>10.1021/la200290k</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-6098-983X</orcidid><orcidid>https://orcid.org/0000-0002-5939-5065</orcidid><orcidid>https://orcid.org/0000-0001-8358-9903</orcidid><orcidid>https://orcid.org/0000-0001-6844-3762</orcidid></addata></record> |
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subjects | Adsorption Animals Biofouling - prevention & control Cattle Chemical Sciences Chemistry Exact sciences and technology General and physical chemistry Gold - chemistry Interfaces: Adsorption, Reactions, Films, Forces Molecular Structure Other Particle Size Propylene Glycols - chemical synthesis Propylene Glycols - chemistry Serum Albumin, Bovine - chemistry Solid-liquid interface Stainless Steel - chemistry Surface physical chemistry Surface Properties |
title | Highly Hydrophilic Surfaces from Polyglycidol Grafts with Dual Antifouling and Specific Protein Recognition Properties |
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