Journal
CARBOHYDRATE POLYMERS
Volume 93, Issue 2, Pages 718-730Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.carbpol.2012.12.055
Keywords
Non-woven textile; Layer-by-layer; Drug release system; Chitosan; Cyclodextrin polymer; OWLS
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Funding
- University of Lille 1
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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 beta-cyclodextrin polymer (polyCTR-beta CD) as polyanion on the other hand. In a second approach, a TBBA/polyCTR-beta CD 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-beta CD complex was applied instead of polyCTR-beta CD 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. (C) 2012 Elsevier Ltd. All rights reserved.
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