Biocidal Activity of Tannic Acid-Prepared Silver Nanoparticles towards Pathogens Isolated from Patients with Exacerbations of Chronic Rhinosinusitis.
Joanna SzaleniecAgnieszka GibałaJoanna StalinskaMagdalena OćwiejaPaulina ŻeliszewskaJustyna DrukałaMaciej SzaleniecTomasz GosiewskiPublished in: International journal of molecular sciences (2022)
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.
Keyphrases
- silver nanoparticles
- chronic rhinosinusitis
- gram negative
- multidrug resistant
- escherichia coli
- acinetobacter baumannii
- klebsiella pneumoniae
- pseudomonas aeruginosa
- cystic fibrosis
- antimicrobial resistance
- chronic obstructive pulmonary disease
- staphylococcus aureus
- drug resistant
- biofilm formation
- induced apoptosis
- oxidative stress
- genetic diversity
- high throughput
- hepatitis b virus
- cell proliferation
- liver failure
- mass spectrometry
- cell cycle arrest
- acute respiratory distress syndrome
- candida albicans
- intensive care unit
- endoplasmic reticulum stress
- high resolution
- drug induced