Cited by 126Antimicrobial agents and applicationsPolymer Surface Interaction StudiesMarine Biology and Environmental Chemistry

Non-leaching antimicrobial surfaces through polydopamine bio-inspired coating of quaternary ammonium salts or an ultrashort antimicrobial lipopeptide

Shalev, Tal, Gopin, Anna, Bauer, Michael, Stark, Robert W., Rahimipour, Shai·2012·J. Mater. Chem.

Abstract

Bacterial fouling on surfaces significantly increases the resistance of bacteria toward antibiotics, which leads to medical complications and a corresponding financial burden. Here, we report on a general and robust technique for facile modification of various surfaces with different antibacterial agents. Our approach in this study was inspired by the strong adhesion of mussel adhesion proteins (MAPs) to many types of surfaces, including metals, polymers, and inorganic materials. Thus, glass and polymeric slides were dip-coated with dopamine, as a MAP mimic, and the resulting surfaces were characterized. The reactivity of dopamine-coated surfaces toward nucleophilic addition was then confirmed by reacting them with fluorescent probes containing either a free amino or a free thiol group. Laser scanning confocal microscopy (LSCM), X-ray photoelectron spectroscopy (XPS), confocal Raman microscopy, matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectroscopy, and cyclic voltammetry studies collectively suggested that the probes had covalently attached to the surfaces. Fabrication of dopamine-coated surfaces with an antibacterial quaternary amine or an ultrashort lipopeptide analog generated surfaces that effectively kill Escherichia coli and Staphylococcus aureuscells on contact. Moreover, minimal leaching of the fabricated agent was detected after prolonged incubation. This technique could be further developed to a “paint-like” or self-assembling mono…

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Registry

Crossref · 10.1039/c1jm13994k

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  • The first model exhibits a "covalent bonding" polymerization fashion where DA is polymerized via 5,6-dihydroxyindole monomers following further oxidization and subsequent intermolecular cross-linking of PDA.

    “The first model exhibits a “covalent bonding” polymerization fashion where DA is polymerized via 5,6-dihydroxyindole monomers following further oxidization and subsequent intermolecular cross-linking of PDA [29, 40–44].”

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Authors
Shalev, T., Gopin, A., Bauer, M., Stark, R. W., & Rahimipour, S.
Affiliations
  • Bar-Ilan University (IL)
  • Center for NanoScience (DE)
Corresponding author
Rahimipour, Shai
Venue
J. Mater. Chem.
Published
2012
Volume
22
Issue
5
Pages
2026-2032
ISSN
  • 0959-9428 (ISSN-L)
  • 1364-5501
OpenAlex
W1966920367
Cited by
126
References
2
Citations by year
2026: 1 · 2025: 2 · 2024: 5 · 2023: 6 · 2022: 9 · 2021: 14 · 2020: 10 · 2019: 9 · 2018: 10 · 2017: 8 · 2016: 10 · 2015: 14 · 2014: 17 · 2013: 6 · 2012: 5
FWCI
4.21
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Materials Chemistry (publishedVersion)
  • Open access LMU (Ludwid Maxmilian's Universitat Munchen) (submittedVersion)
Topics
  • Physical Sciences › Chemistry › Organic Chemistry › Antimicrobial agents and applications
  • Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
  • Physical Sciences › Engineering › Ocean Engineering › Marine Biology and Environmental Chemistry
Keywords
antimicrobial surfaces, polydopamine coating, quaternary ammonium compounds, antimicrobial lipopeptides, Escherichia coli, Staphylococcus aureus, bacterial fouling, dip coating, covalent surface modification

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