Synthesis and characterization of biomimetic nanogels for immunorecognition

Autor: Muriel Lansalot, Claudia S. O. Silva, M. Ângela Taipa, José M. G. Martinho, Jaqueline Q. Garcia
Přispěvatelé: Laboratoire de Chimie, Catalyse, Polymères et Procédés, R 5265 (C2P2), Centre National de la Recherche Scientifique (CNRS)-École supérieure de Chimie Physique Electronique de Lyon (CPE)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut de Chimie du CNRS (INC), CQFM, Centro de Química-Física Molecular, IN - Institute of Nanosciences and Nanotechnology, Centro de Química-Física Molecular
Jazyk: angličtina
Rok vydání: 2013
Předmět:
Zdroj: Colloids and Surfaces B: Biointerfaces
Colloids and Surfaces B: Biointerfaces, Elsevier, 2013, 112, pp.264-271. ⟨10.1016/j.colsurfb.2013.08.003⟩
ISSN: 0927-7765
DOI: 10.1016/j.colsurfb.2013.08.003⟩
Popis: Biomimetic nanoparticles are promising materials for biomedical and biotechnological applications. Cationic poly(N-isopropylacrylamide) (PNIPAM) nanogels containing charged amine groups brought by addition of 2-aminoethylmethacrylate hydrochloride (AEMH) or N-(3-aminopropyl) methacrylamide hydrochloride (APMH) as co-monomers were prepared by surfactant-free precipitation polymerization. The influence of the relative amount and mode of addition of the co-monomer on both the size and the amine group density of the nanogel particles was studied. Two nanogels, one prepared using APMH (1%mol/mol NIPAM, in batch) and another with AEMH (2%mol/mol NIPAM, by shot addition) as co-monomers, were selected for the covalent coupling of a Protein L-mimic ligand to free amine groups on the particles. The ability of the synthesized biomimetic nanoparticles for recognizing and binding human IgG (hIgG) molecules was assessed and the selectivity toward immunoglobulin molecules evaluated.
Databáze: OpenAIRE