Well‐controlled amphiphilic block glycopolymers and their molecular recognition with lectins

2010; Wiley; Volume: 48; Issue: 16 Linguagem: Inglês

10.1002/pola.24143

ISSN

1099-0518

Autores

Orietta León, Vanesa Bordegé, Alexandra Muñoz‐Bonilla, Manuel Sánchez‐Chaves, Marta Fernández‐García,

Tópico(s)

Chemical Synthesis and Analysis

Resumo

Abstract The atom transfer radical polymerization of an unprotected glycomonomer, 2‐{[( D ‐glucosamin‐2 N ‐yl)carbonyl]oxy}ethyl methacrylate (HEMAGl) is firstly reported. Controlled polymerizations were performed with the CuBr/ N,N,N′,N′,N′ ‐pentamethyldiethylene triamine catalytic system with ethyl 2‐bromoisobutyrate and 1,2‐bis(bromoisobutyryloxy) ethane as mono and difunctional initiators in DMF solutions (80% w/w) at 40 and 50 °C, respectively. The polymerization of HEMAGl resulted in a controlled polymerization with linear kinetics, molecular weights which increase with conversion and narrow polydispersity indexes. Mono and difunctional PHEMAGl macroinitiators were used to synthesize the amphiphilic di and triblock glycopolymers with n ‐butyl acrylate, verifying their living character. The self‐assembly of these glycopolymers in distilled water and in 0.1M NaCl solutions was studied by dynamic light scattering, showing the role of hydrogen bonds and the hydrophobic parts. In addition, their interaction with Concanavalin A lectin was examined, demonstrating the influence of molecular weight and copolymer composition. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3623–3631, 2010

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