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Polysaccharide-based antibiofilm surfaces

Abstract : Surface treatment by natural or modified polysaccharide polymers is a promising means to fight against implant-associated biofilm infections. The present review focuses on polysaccharide-based coatings that have been proposed over the last ten years to impede biofilm formation on material surfaces exposed to bacterial contamination. Anti-adhesive and bactericidal coatings are considered. Besides classical hydrophilic coatings based on hyaluronic acid and heparin, the promising anti-adhesive properties of the algal polysaccharide ulvan are underlined. Surface functionalization by antimicrobial chitosan and derivatives is extensively surveyed, in particular chitosan association with other polysaccharides in layer-by-layer assemblies to form both anti-adhesive and bactericidal coatings. Statement of Significance Bacterial contamination of surfaces, leading to biofilm formation, is a major problem in fields as diverse as medicine, first, but also food and cosmetics. Many prophylactic strategies have emerged to try to eliminate or reduce bacterial adhesion and biofilm formation on surfaces of materials exposed to bacterial contamination, in particular implant materials. Polysaccharides are widely distributed in nature. A number of these natural polymers display antibiofilm properties. Hence, surface treatment by natural or modified polysaccharides is a promising means to fight against implant-associated biofilm infections. The present manuscript is an in-depth look at polysaccharide-based antibiofilm surfaces that have been proposed over the last ten years. This review, which is a novelty compared to published literature, will bring well documented and updated information to readers of Acta Biomaterialia.
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Contributor : Laurent Lebrun <>
Submitted on : Tuesday, November 19, 2019 - 11:56:53 AM
Last modification on : Thursday, July 2, 2020 - 3:30:10 AM



Guy-Alain Junter, Pascal Thebault, Laurent Lebrun. Polysaccharide-based antibiofilm surfaces. Acta Biomaterialia, Elsevier, 2016, 30, pp.13-25. ⟨10.1016/j.actbio.2015.11.010⟩. ⟨hal-02370053⟩



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