Unknown

Dataset Information

0

Maltodextrin enhances biofilm elimination by electrochemical scaffold.


ABSTRACT: Electrochemical scaffolds (e-scaffolds) continuously generate low concentrations of H2O2 suitable for damaging wound biofilms without damaging host tissue. Nevertheless, retarded diffusion combined with H2O2 degradation can limit the efficacy of this potentially important clinical tool. H2O2 diffusion into biofilms and bacterial cells can be increased by damaging the biofilm structure or by activating membrane transportation channels by exposure to hyperosmotic agents. We hypothesized that e-scaffolds would be more effective against Acinetobacter baumannii and Staphylococcus aureus biofilms in the presence of a hyperosmotic agent. E-scaffolds polarized at -600?mVAg/AgCl were overlaid onto preformed biofilms in media containing various maltodextrin concentrations. E-scaffold alone decreased A. baumannii and S. aureus biofilm cell densities by (3.92?±?0.15) log and (2.31?±?0.12) log, respectively. Compared to untreated biofilms, the efficacy of the e-scaffold increased to a maximum (8.27?±?0.05) log reduction in A. baumannii and (4.71?±?0.12) log reduction in S. aureus biofilm cell densities upon 10?mM and 30?mM maltodextrin addition, respectively. Overall ~55% decrease in relative biofilm surface coverage was achieved for both species. We conclude that combined treatment with electrochemically generated H2O2 from an e-scaffold and maltodextrin is more effective in decreasing viable biofilm cell density.

SUBMITTER: Sultana ST 

PROVIDER: S-EPMC5080540 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

Maltodextrin enhances biofilm elimination by electrochemical scaffold.

Sultana Sujala T ST   Call Douglas R DR   Beyenal Haluk H  

Scientific reports 20161026


Electrochemical scaffolds (e-scaffolds) continuously generate low concentrations of H<sub>2</sub>O<sub>2</sub> suitable for damaging wound biofilms without damaging host tissue. Nevertheless, retarded diffusion combined with H<sub>2</sub>O<sub>2</sub> degradation can limit the efficacy of this potentially important clinical tool. H<sub>2</sub>O<sub>2</sub> diffusion into biofilms and bacterial cells can be increased by damaging the biofilm structure or by activating membrane transportation chann  ...[more]

Similar Datasets

2017-01-18 | GSE79750 | GEO
| S-EPMC6886667 | biostudies-literature
| S-EPMC11217050 | biostudies-literature
| S-EPMC7179276 | biostudies-literature
| S-EPMC3717969 | biostudies-literature
| S-EPMC9763052 | biostudies-literature
| S-EPMC6389966 | biostudies-literature
| S-EPMC6519109 | biostudies-literature
| S-EPMC9868040 | biostudies-literature
| S-EPMC7641139 | biostudies-literature