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Antimicrobial behavior of novel surfaces generated by electrophoretic deposition and breakdown anodization
Journal article   Open access   Peer reviewed

Antimicrobial behavior of novel surfaces generated by electrophoretic deposition and breakdown anodization

Jessamine Q. Flores, Young Soo Joung, Nichola M. Kinsinger, Xinglin Lu, Cullen R. Buie and Sharon L. Walker
Colloids and surfaces, B, Biointerfaces, v 134, pp 204-212
01 Oct 2015
PMID: 26196093
url
https://escholarship.org/uc/item/7vn9s8jqView

Abstract

Bacterial adhesion Biofilms Biofouling Parallel plate flow chamber Titanium oxide polydimethylsiloxane
[Display omitted] •Bacterial attachment evaluated for surfaces with micro- and nano-scale structures.•Higher attachment on superhydrophilic surfaces than the hydrophobic surfaces.•Possible negative correlation with increase roughness in hydrophobic surfaces. Biofilms have devastating impacts on many industries such as increased fuel consumption and damage to surfaces in maritime industries. Ideal biofouling management is inhibition of initial bacterial attachment. The attachment of a model marine bacterium (Halomonas pacfica g) was investigated to evaluate the potential of these new novel surfaces to resist initial bacterial adhesion. Novel engineered surfaces were generated via breakdown anodization or electrophoretic deposition, to modify three parameters: hydrophobicity, surface chemistry, and roughness. Mass transfer rates were determined using a parallel plate flow chamber under relevant solution chemistries. The greatest deposition was observed on the superhydrophilic surface, which had micro- and nano-scale hierarchical structures composed of titanium oxide deposited on a titanium plate. Conversely, one of the hydrophobic surfaces with micro-porous films overlaid with polydimethylsiloxane appeared to be most resistant to cell attachment.

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Collaboration types
Domestic collaboration
International collaboration
Web of Science research areas
Biophysics
Chemistry, Physical
Materials Science, Biomaterials
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