4.7 Article

Biocidal Activity of Tannic Acid-Prepared Silver Nanoparticles towards Pathogens Isolated from Patients with Exacerbations of Chronic Rhinosinusitis

期刊

出版社

MDPI
DOI: 10.3390/ijms232315411

关键词

chronic rhinosinusitis; exacerbations; microbiome; microbiota; bacteria; antibiotic resistance; silver nanoparticles; tannic acid

资金

  1. Jagiellonian University Medical College statutory funds [N41/DBS/000462]
  2. InterDokMed - European Social Fund [POWR.03.02.00-00-I013/16]

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This study assessed the biological activity of tannic acid-prepared silver nanoparticles (TA-AgNPs) on sinonasal pathogens and nasal epithelial cells. The results showed that TA-AgNPs were effective against most pathogens isolated from patients with acute exacerbations of chronic rhinosinusitis (AECRS) at non-toxic concentrations to human cells. However, prolonged exposure to TA-AgNPs increased toxicity to nasal epithelial cells and enabled some pathogens to resist their biocidal action. Sensitivity testing may be necessary before application.
The microbiome's significance in chronic rhinosinusitis (CRS) is unclear. Antimicrobials are recommended in acute exacerbations of the disease (AECRS). Increasing rates of antibiotic resistance have stimulated research on alternative therapeutic options, including silver nanoparticles (AgNPs). However, there are concerns regarding the safety of silver administration. The aim of this study was to assess the biological activity of tannic acid-prepared AgNPs (TA-AgNPs) towards sinonasal pathogens and nasal epithelial cells (HNEpC). The minimal inhibitory concentration (MIC) for pathogens isolated from patients with AECRS was approximated using the well diffusion method. The cytotoxicity of TA-AgNPswas evaluated using an MTT assay and trypan blue exclusion. A total of 48 clinical isolates and 4 reference strains were included in the study (Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Klebsiellaoxytoca, Acinetobacter baumannii, Serratia marcescens, Enterobacter cloacae). The results of the studies revealed that the MIC values differed between isolates, even within the same species. All the isolates were sensitive to TA-AgNPs in concentrations non-toxic to human cells during 24 h exposition. However, 48 h exposure to TA-AgNPs increased toxicity to HNEpC, narrowing their therapeutic window and enabling 19% of pathogens to resist the TA-AgNPs' biocidal action. It was concluded that TA-AgNPs are non-toxic for the investigated eukaryotic cells after short-term exposure and effective against most pathogens isolated from patients with AECRS, but sensitivity testing may be necessary before application.

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