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Multilayered textile coating based on a ß-cyclodextrin polyelectrolyte for the controlled release of drugs.
Martin, Adeline; Tabary, Nicolas; Leclercq, Laurent; Junthip, Jatupol; Degoutin, Stéphanie; Aubert-Viard, François; Cazaux, Frédéric; Lyskawa, Joël; Janus, Ludovic; Bria, Marc; Martel, Bernard.
Afiliación
  • Martin A; Université Lille 1, Unité Matériaux et Transformations UMR CNRS 8207, Villeneuve d'Ascq, France.
Carbohydr Polym ; 93(2): 718-30, 2013 Apr 02.
Article en En | MEDLINE | ID: mdl-23499116
The aim of this work was to develop the formation of multilayered coating incorporating a cyclodextrin polyelectrolyte onto a non-woven polyethylene terephthalate (PET) textile support in order to obtain reservoir and sustained release properties towards bioactive molecules. We optimized the multilayer assembly immobilization onto the PET surface according to the layer-by-layer (LbL) deposition process. After a pre-treatment of the textile support aiming to offer a sufficient ionic character to the surface, it was alternatively immersed into two polyelectrolytes aqueous solutions consisting of chitosan (CHT) as polycation on the one hand, and a ß-cyclodextrin polymer (polyCTR-ßCD) as polyanion on the other hand. In a second approach, a TBBA/polyCTR-ßCD complex (4-tert-butylbenzoic acid, TBBA) was used in order to load the system with a drug model whose kinetics of release was assessed. Gravimetry, microscopy, OWLS, colorimetric titration, infrared and zetametry were used as characterization techniques. An effective deposition on the textile surface due to ionic interactions with alternation of up to 10 layers of each of both polyelectrolytes was clearly evidenced. However, we observed that layer formation occurred to a lesser extent when TBBA/polyCTR-ßCD complex was applied instead of polyCTR-ßCD alone. The release study showed that drug reservoir properties and release kinetics could be controlled by the number of layers in the system and that TBBA release was faster than the multilayered coating degradation.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Portadores de Fármacos / Beta-Ciclodextrinas Idioma: En Revista: Carbohydr Polym Año: 2013 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Portadores de Fármacos / Beta-Ciclodextrinas Idioma: En Revista: Carbohydr Polym Año: 2013 Tipo del documento: Article País de afiliación: Francia