Characterization, antibiofilm and biocompatibility properties of chitosan hydrogels loaded with silver nanoparticles and ampicillin: an alternative protection to central venous catheters
Article
Overview
Research
Identity
Additional Document Info
View All
Overview
abstract
The purpose of this study was to generate novel chitosan hydrogels (CHs) loaded with silver nanoparticles (AgNPs) and ampicillin (AMP) to prevent early formation of biofilms. AgNPs and CHs were characterized by UV-Vis, DLS, TEM, rheology, FT-IR, Raman, and SEM. The antibiofilm effect of the formulations was investigated against four multidrug-resistant and extensively drug-resistant pathogens using a colony biofilm, a high cell density and gradients model. Also, their hemostatic properties and cytotoxic effect were evaluated. Rheology results showed that CHs with AgNPs and AMP are typical non-Newtonian pseudoplastic fluids. The CH with 25 ppm of AgNPs and 50 ppm AMP inhibited the formation of biofilms of Acinetobacter baumannii, Enterococcus faecium and Staphylococcus epidermidis, while a ten-fold increase of the antimicrobial%27s concentration was needed to inhibit the biofilm of the β-lactamase positive Enterobacter cloacae. Further, CH with 250 ppm of AgNPs and 500 ppm AMP showed anticoagulant effect, and it was shown that all formulations were biocompatible. Besides to previous reports that described the bioadhesion properties of chitosan, these results suggest that AgNPs and AMP CHs loaded could be used as prophylactic treatment in patients with central venous catheter (CVC), inhibiting the formation of biofilms in their early stages, in addition to their anticoagulant effect and biocompatibility, those properties could keep the functionality of CVC helping to prevent complications such as sepsis and thrombosis. © 2020 Elsevier B.V.
The purpose of this study was to generate novel chitosan hydrogels (CHs) loaded with silver nanoparticles (AgNPs) and ampicillin (AMP) to prevent early formation of biofilms. AgNPs and CHs were characterized by UV-Vis, DLS, TEM, rheology, FT-IR, Raman, and SEM. The antibiofilm effect of the formulations was investigated against four multidrug-resistant and extensively drug-resistant pathogens using a colony biofilm, a high cell density and gradients model. Also, their hemostatic properties and cytotoxic effect were evaluated. Rheology results showed that CHs with AgNPs and AMP are typical non-Newtonian pseudoplastic fluids. The CH with 25 ppm of AgNPs and 50 ppm AMP inhibited the formation of biofilms of Acinetobacter baumannii, Enterococcus faecium and Staphylococcus epidermidis, while a ten-fold increase of the antimicrobial's concentration was needed to inhibit the biofilm of the β-lactamase positive Enterobacter cloacae. Further, CH with 250 ppm of AgNPs and 500 ppm AMP showed anticoagulant effect, and it was shown that all formulations were biocompatible. Besides to previous reports that described the bioadhesion properties of chitosan, these results suggest that AgNPs and AMP CHs loaded could be used as prophylactic treatment in patients with central venous catheter (CVC), inhibiting the formation of biofilms in their early stages, in addition to their anticoagulant effect and biocompatibility, those properties could keep the functionality of CVC helping to prevent complications such as sepsis and thrombosis. © 2020 Elsevier B.V.
publication date
funding provided via
published in
Research
keywords
Biofilm; central venous catheter; chitosan; cytotoxicity; hemostatic properties; silver nanoparticles Biocompatibility; Biofilms; Catheters; Chitosan; Drug delivery; Elasticity; Hydrogels; Metal nanoparticles; Non Newtonian flow; Silver nanoparticles; Drug-resistant pathogens; Enterobacter cloacae; Enterococcus faecium; High cell density; Multidrug resistants; Pseudoplastic fluid; Silver nanoparticles (AgNps); Staphylococcus epidermidis; Silver compounds; ampicillin; beta lactamase; chitosan; hydrogel; silver nanoparticle; Acinetobacter baumannii; antibiofilm activity; anticoagulation; antimicrobial activity; Article; biocompatibility; biofilm; bloodstream infection; cell density; controlled study; cytotoxicity; drug delivery system; drug formulation; drug screening; Enterobacter cloacae; Enterococcus faecium; fibroblast; flow kinetics; Fourier transform infrared spectroscopy; human; human cell; multidrug resistant bacterium; nonhuman; photon correlation spectroscopy; priority journal; Raman spectrometry; retrospective study; scanning electron microscopy; sepsis; Staphylococcus epidermidis; thrombosis; transmission electron microscopy; ultraviolet visible spectroscopy
Identity
Digital Object Identifier (DOI)
PubMed ID
Additional Document Info
start page
end page
volume