Pluronic F-127 Enhances the Antifungal Activity of Fluconazole against Resistant Candida Strains.
Katarzyna Hanna MalecAleksandra MikołajczykDominik MarciniakAgnieszka Gawin-MikołajewiczAgnieszka Matera-WitkiewiczBożena KarolewiczUrszula NawrotYaroslav Z KhimyakKarol P NartowskiPublished in: ACS infectious diseases (2023)
Candida strains as the most frequent causes of infections, along with their increased drug resistance, pose significant clinical and financial challenges to the healthcare system. Some polymeric excipients were reported to interfere with the multidrug resistance mechanism. Bearing in mind that there are a limited number of marketed products with fluconazole (FLU) for the topical route of administration, Pluronic F-127 (PLX)/FLU formulations were investigated in this work. The aims of this study were to investigate (i) whether PLX-based formulations can increase the susceptibility of resistant Candida strains to FLU, (ii) whether there is a correlation between block polymer concentration and the antifungal efficacy of the FLU-loaded PLX formulations, and (iii) what the potential mode of action of PLX assisting FLU is. The yeast growth inhibition upon incubation with PLX formulations loaded with FLU was statistically significant. The highest efficacy of the azole agent was observed in the presence of 5.0 and 10.0% w/v of PLX. The upregulation of the CDR1/CDR2 genes was detected in the investigated Candida strains, indicating that the efflux of the drug from the fungal cell was the main mechanism of the resistance.
Keyphrases
- candida albicans
- biofilm formation
- escherichia coli
- drug delivery
- cancer therapy
- poor prognosis
- cell proliferation
- wound healing
- staphylococcus aureus
- stem cells
- dna methylation
- risk assessment
- atomic force microscopy
- cell therapy
- mesenchymal stem cells
- long non coding rna
- cystic fibrosis
- saccharomyces cerevisiae
- pseudomonas aeruginosa
- transcription factor
- drug induced
- high speed
- childhood cancer