Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/7103
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dc.contributor.authorTomić, Ninaen_US
dc.contributor.authorStevanović, Magdalena Men_US
dc.contributor.authorFilipović, Nenaden_US
dc.contributor.authorGanić, Teaen_US
dc.contributor.authorNikolić, Biljanaen_US
dc.contributor.authorGajić, Inaen_US
dc.contributor.authorĆulafić, Dragana Mitićen_US
dc.date.accessioned2024-02-26T08:30:40Z-
dc.date.available2024-02-26T08:30:40Z-
dc.date.issued2024-02-16-
dc.identifier.issn2079-4991-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/7103-
dc.description.abstractIn this work, we synthesized a new composite material comprised of previously formulated resveratrol nanobelt-like particles (ResNPs) and selenium nanoparticles (SeNPs), namely ResSeNPs. Characterization was provided by FESEM and optical microscopy, as well as by UV-Vis and FTIR spectroscopy, the last showing hydrogen bonds between ResNPs and SeNPs. DPPH, TBA, and FRAP assays showed excellent antioxidative abilities with ResNPs and SeNPs contributing mainly to lipid peroxidation inhibition and reducing/scavenging activity, respectively. The antibacterial effect against common medicinal implant colonizers pointed to notably higher activity against Staphylococcus isolates (minimal inhibitory concentrations 0.75-1.5%) compared to tested gram-negative species (Escherichia coli and Pseudomonas aeruginosa). Antibiofilm activity against S. aureus, S. epidermidis, and P. aeruginosa determined in a crystal violet assay was promising (up to 69%), but monitoring of selected biofilm-related gene expression (pelA and algD) indicated the necessity of the involvement of a larger number of genes in the analysis in order to further establish the underlying mechanism. Although biocompatibility screening showed some cytotoxicity and genotoxicity in MTT and alkaline comet assays, respectively, it is important to note that active antioxidative and antibacterial/antibiofilm concentrations were non-cytotoxic and non-genotoxic in normal MRC-5 cells. These results encourage further composite improvements and investigation in order to adapt it for specific biomedical purposes.en_US
dc.language.isoenen_US
dc.publisherMPDIen_US
dc.relation.ispartofNanomaterials (Basel, Switzerland)en_US
dc.subjectantibiofilmen_US
dc.subjectantioxidativeen_US
dc.subjectbiocompatibilityen_US
dc.subjectresveratrolen_US
dc.subjectselenium nanoparticlesen_US
dc.titleResveratrol/Selenium Nanocomposite with Antioxidative and Antibacterial Propertiesen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.3390/nano14040368-
dc.identifier.pmid38392741-
dc.description.rankM21en_US
dc.description.impact5.3en_US
dc.description.startpage368en_US
dc.relation.issn2079-4991en_US
dc.description.volume14en_US
dc.description.issue4en_US
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Microbiology-
crisitem.author.deptChair of Microbiology-
crisitem.author.orcid0000-0001-8600-4392-
crisitem.author.orcid0000-0003-1765-2454-
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