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Polymer mediated peptide immobilization onto amino-containing N-isopropylacrylamide-styrene core-shell particles
Authors:Silvina Rossi  Carmen Lorenzo-Ferreira  Julio Battistoni  Abdelhamid Elaïssari  Christian Pichot  Thierry Delair
Affiliation:(1) Catedra de Immunologia—Facultades de Química y Ciencias Instituto de Higiene A, Navarro, 3051, C.P. 11600 Montevideo, Uruguay;(2) UMR-2142, CNRS-bioMérieux, ENS de Lyon, allée d"rsquo"Italie, 46, 69364 Lyon, France
Abstract:Monodisperse cationic core-shell latex particles have been prepared using a shot polymerization process, with N-(3-aminopropyl)-methacrylamide-hydrochloride (APMH) as the functional monomer. The final latexes were characterized with respect to final polymerization conversion, water soluble polymer formation, particle size and size distribution, surface charge density and electrokinetic properties. Then the covalent grafting of maleic anhydride-alt-methyl vinyl ether (MAMVE) copolymer onto aminated latex particles was investigated. The most efficient conditions to obtain derivatised particles with no alteration of the colloidal stability were to control both polymer amount/latex particles concentration ratio and the mixing method of the two species. The charge inversion of the hydrolysed MAMVE functionalized particles was demonstrated by measuring the electrophoretic mobility as a function of pH. Finally, the covalent binding approach was implemented with peptide-MAMVE conjugates, confirming the great potential of this promising methodology for the preparation of reactive latex particles bearing peptides.
Keywords:Temperature sensitive  Core-shell latex  Reactive copolymer  Covalent coupling  Peptides
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