Cargando…

Fabrication of low-fouling, high-loading polymeric surfaces through pH-controlled RAFT

Low-fouling and high-loading surfaces are increasingly important for biosensing and blood purification technologies. Selective and efficient target binding from complex media can be achieved with poly(carboxybetaine) (pCB) surfaces that consist of a dense brush layer to resist non-specific protein a...

Descripción completa

Detalles Bibliográficos
Autores principales: Jesmer, Alexander H., Huynh, Vincent, Wylie, Ryan G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054213/
https://www.ncbi.nlm.nih.gov/pubmed/35520404
http://dx.doi.org/10.1039/d0ra02693j
Descripción
Sumario:Low-fouling and high-loading surfaces are increasingly important for biosensing and blood purification technologies. Selective and efficient target binding from complex media can be achieved with poly(carboxybetaine) (pCB) surfaces that consist of a dense brush layer to resist non-specific protein adsorption and a sparse “mushroom” upper layer for high-density capture agent immobilization (i.e. high-loading). We developed pH-controlled surface-reversible addition–fragmentation chain-transfer (S-RAFT) polymerization to simplify fabrication of multi-modal, low-fouling and high-loading pCB surfaces without the need for quenching or re-initiation steps, toxic transition metals or light irradiation. Multi-modal polymer layers were produced through partial polymer termination by temporarily raising the pH to aminolyse a fraction of dormant chain transfer agents (CTAs); remaining polymer chains with intact CTAs continued uninterrupted extension to create the “mushroom” upper layer. The multi-modal pCB surfaces were low-fouling towards proteins (<6.7 ng cm(−2)), and macrophages. Compared to mono-modal brush surfaces, multi-modal pCB surfaces were high-loading with 5-fold greater capture agent immobilization (e.g. antibody) and 4-fold greater target binding (e.g. biotin-fluorescein).