Mannosylated brush copolymers based on poly(ethylene glycol) and poly(ε-caprolactone) as multivalent lectin-binding nanomaterials

Autor: Wanda Celentano, Stefania Ordanini, Anna Bernardi, Francesco Cellesi
Jazyk: angličtina
Rok vydání: 2019
Předmět:
Glycopolymer
General Physics and Astronomy
Nanoparticle
ring-opening polymerization (rop)
02 engineering and technology
010402 general chemistry
lcsh:Chemical technology
01 natural sciences
lcsh:Technology
Full Research Paper
chemistry.chemical_compound
glycopolymer
Copolymer
Nanotechnology
General Materials Science
lcsh:TP1-1185
atom transfer radical polymerization (atrp)
Electrical and Electronic Engineering
lcsh:Science
biology
poly(ethylene glycol)
lcsh:T
Ligand binding assay
021001 nanoscience & nanotechnology
Combinatorial chemistry
lcsh:QC1-999
0104 chemical sciences
Nanoscience
chemistry
Concanavalin A
biology.protein
lectin
lcsh:Q
atom transfer radical polymerization (ATRP)
poly(ε-caprolactone)
ring-opening polymerization (ROP)
0210 nano-technology
Ethylene glycol
Caprolactone
lcsh:Physics
Macromolecule
Zdroj: Beilstein Journal of Nanotechnology, Vol 10, Iss 1, Pp 2192-2206 (2019)
Beilstein Journal of Nanotechnology
ISSN: 2190-4286
Popis: A class of linear and four-arm mannosylated brush copolymers based on poly(ethylene glycol) and poly(ε-caprolactone) is presented here. The synthesis through ring-opening and atom transfer radical polymerizations provided high control over molecular weight and functionality. A post-polymerization azide–alkyne cycloaddition allowed for the formation of glycopolymers with different mannose valencies (1, 2, 4, and 8). In aqueous media, these macromolecules formed nanoparticles that were able to bind lectins, as investigated by concanavalin A binding assay. The results indicate that carbohydrate–lectin interactions can be tuned by the macromolecular architecture and functionality, hence the importance of these macromolecular properties in the design of targeted anti-pathogenic nanomaterials.
Databáze: OpenAIRE