Inhibition of bacterial biofilms by carboxymethyl chitosan combined with silver, zinc and copper salts

• Published in: International journal of biological macromolecules 2017-12, Vol.105 (Pt 1), p.385-392
• Main Authors: Gonçalves, Randys Caldeira, da Silva, Diego Pereira, Signini, Roberta, Naves, Plínio Lázaro Faleiro
• Format: Article
• Language: English
• Subjects: Animals; Antimicrobial activity; Artemia; Bacteria - drug effects; Biofilm inhibition; Biofilms - drug effects; Biofilms - growth & development; Carboxymethyl chitosan; Chitosan - analogs & derivatives; Chitosan - chemistry; Chitosan - pharmacology; Chitosan - toxicity; Copper - chemistry; Metallic salts; Metals, Heavy - chemistry; Microbial Sensitivity Tests; Silver - chemistry; Sulfates - chemistry; Toxicity; Zinc - chemistry
• ISSN: 0141-8130; 1879-0003
• DOI: 10.1016/j.ijbiomac.2017.07.048

•CMCh did not show toxicity to A. salina (LC50>2400μgmL−1).•CMCh was not able to inhibit the growth of Gram-positive or Gram-negative bacteria.•Gram-negative biofilms were more susceptible to compounds than Gram-positive.•CMCh inhibited 80% of biofilm of B. cepacia, E. coli, S. aureus and K. rhizophila. Investigation of the antimicrobial action of carboxymethyl chitosan (CMCh) is among the alternative approaches in the control of pathogenic microorganisms. This study aimed to screen the toxicity using the brine shrimp lethality assay and to investigate the inhibitory activity of carboxymethyl in isolation or in combination with silver nitrate, copper sulfate and zinc sulfate on biofilm formation by Staphylococcus aureus ATCC 6538, Staphylococcus epidermidis ATCC 12228, Kocuria rhizophila ATCC 9341, Pseudomonas aeruginosa ATCC 9027, Escherichia coli ATCC 25312, and Burkholderia cepacia ATCC 17759. The CMCh was obtained by reacting chitosan with monochloroacetic acid under alkaline conditions, and the occurrence of carboxymethylation was evidenced by FTIR and 1H NMR spectroscopy. The CMCh was combined with metallic salts (AgNO3, CuSO4·5H2O and ZnSO4) to perform the bioassays to screen the toxicity, to determine the minimum inhibitory concentration and the impact of sub-inhibitory concentrations against biofilm formation. Although CMCh did not show inhibitory activity against bacterial growth, it had an interesting level of inhibition of bacterial biofilm. The results suggest that sub-inhibitory concentrations of compounds were effective against biofilm formation.