TY - JOUR
T1 - Polyvalent incorporation of anionic β-cyclodextrin polymers into layer-by-layer coatings
AU - Pédehontaa-Hiaa, Guillaume
AU - Gaudière, Fabien
AU - Khelif, Rim
AU - Morin-Grognet, Sandrine
AU - Labat, Béatrice
AU - Lutzweiler, Gaëtan
AU - Le Derf, Franck
AU - Atmani, Hassan
AU - Morin, Christophe
AU - Ladam, Guy
PY - 2023/5/5
Y1 - 2023/5/5
N2 - As versatile compounds forming host-guest complexes with a wide variety of hydrophobic molecules, cyclodextrins are widespread candidates to confer functionalities to surfaces, particularly for drug delivery applications in the field of biomaterials, and for analytic or preparative purposes in separative sciences. We report here on Layer-by-Layer coatings used to decorate surfaces with β-cyclodextrins, based on their capacity to allow the stress-free immobilization, and to maintain the accessibility and activity of functional components. We incorporated a β-cyclodextrin polymer into the coatings, either as the polyanionic component in association with polycationic polyethyleneimine or poly-l-lysine, or by post-loading into chondroitin sulfate/poly-l-lysine films. The study of the buildup mechanism, the structural features, and the interactions of the coatings with racemic mixtures of chiral hydrophobic compounds, provided evidence of the effective incorporation of the cyclodextrins and of their preserved functionality. The post-loading protocol led to noticeably high amounts of incorporated cyclodextrin polymer, which made it an unique, efficient route to embed cyclodextrins into Layer-by-Layer architectures. All the cyclodextrin-enriched films improved the chromatographic retention of hydrophobic compounds, and the polyethyleneimine/cyclodextrin systems showed additional enantioseparation properties. We view our coatings as relevant candidates for the design of drug nanoreservoirs atop biomaterials, and stationary phases in chromatographic devices.
AB - As versatile compounds forming host-guest complexes with a wide variety of hydrophobic molecules, cyclodextrins are widespread candidates to confer functionalities to surfaces, particularly for drug delivery applications in the field of biomaterials, and for analytic or preparative purposes in separative sciences. We report here on Layer-by-Layer coatings used to decorate surfaces with β-cyclodextrins, based on their capacity to allow the stress-free immobilization, and to maintain the accessibility and activity of functional components. We incorporated a β-cyclodextrin polymer into the coatings, either as the polyanionic component in association with polycationic polyethyleneimine or poly-l-lysine, or by post-loading into chondroitin sulfate/poly-l-lysine films. The study of the buildup mechanism, the structural features, and the interactions of the coatings with racemic mixtures of chiral hydrophobic compounds, provided evidence of the effective incorporation of the cyclodextrins and of their preserved functionality. The post-loading protocol led to noticeably high amounts of incorporated cyclodextrin polymer, which made it an unique, efficient route to embed cyclodextrins into Layer-by-Layer architectures. All the cyclodextrin-enriched films improved the chromatographic retention of hydrophobic compounds, and the polyethyleneimine/cyclodextrin systems showed additional enantioseparation properties. We view our coatings as relevant candidates for the design of drug nanoreservoirs atop biomaterials, and stationary phases in chromatographic devices.
KW - Biofunctional coatings
KW - Polyelectrolyte multilayers
KW - Capillary electrochromatography
KW - Chiral resolution
KW - Nanoreservoirs
U2 - 10.1016/j.colsurfa.2023.131154
DO - 10.1016/j.colsurfa.2023.131154
M3 - Article
SN - 0927-7757
VL - 664
JO - Colloids and Surfaces A: Physicochemical and Engineering Aspects
JF - Colloids and Surfaces A: Physicochemical and Engineering Aspects
M1 - 131154
ER -