posted on 2024-05-09, 08:13authored byAna M. Ferreira, Anna S. Vikulina, Laura Bowker, John A. Hunt, Michael Loughlin, Valeria Puddu, Dmitry Volodkin
Antimicrobial coatings provide protection against microbes
colonization
on surfaces. This can prevent the stabilization and proliferation
of microorganisms. The ever-increasing levels of microbial resistance
to antimicrobials are urging the development of alternative types
of compounds that are potent across broad spectra of microorganisms
and target different pathways. This will help to slow down the development
of resistance and ideally halt it. The development of composite antimicrobial
coatings (CACs) that can host and protect various antimicrobial agents
and release them on demand is an approach to address this urgent need.
In this work, new CACs based on microsized hybrids of calcium carbonate
(CaCO3) and silver nanoparticles (AgNPs) were designed
using a drop-casting technique. Polyvinylpyrrolidone and mucin were
used as additives. The CaCO3/AgNPs hybrids contributed
to endowing colloidal stability to the AgNPs and controlling their
release, thereby ensuring the antibacterial activity of the coatings.
Moreover, the additives PVP and mucin served as a matrix to (i) control
the distribution of the hybrids, (ii) ensure mechanical integrity,
and (iii) prevent the undesired release of AgNPs. Scanning electron
microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared
(FTIR) techniques were used to characterize the 15 μm thick
CAC. The antibacterial activity was determined against Escherichia coli, methicillin-resistant Staphylococcus aureus (MRSA), and Pseudomonas aeruginosa, three bacteria responsible
for many healthcare infections. Antibacterial performance of the hybrids
was demonstrated at concentrations between 15 and 30 μg/cm2. Unloaded CaCO3 also presented bactericidal properties
against MRSA. In vitro cytotoxicity tests demonstrated
that the hybrids at bactericidal concentrations did not affect human
dermal fibroblasts and human mesenchymal stem cell viability. In conclusion,
this work presents a simple approach for the design and testing of
advanced multicomponent and functional antimicrobial coatings that
can protect active agents and release them on demand.