Relevance. Flavonoids represent the largest group of natural molecules with antibacterial action, which can be explained by aggregation of bacterial cells and damage to the bacterial membrane. Modification of antimicrobial drugs with flavonoids may become a promising technique in the fight against antibiotic resistance, since the presence of complex structural complexes in the composition will help hide or reduce the recognition of antibac-terial substances by bacteria. The purpose of the work: To assess the change in morphometric parameters of bacterial cells of P. aeruginosa under the combined effect of anti-bacterial drugs and flavonoids of medicinal plant raw materials. Material and methods: The object of the study were strains of R. aeruginosa grown on meat-peptone agar, which were affected by complexes of flavonoids isolated from Dianthus and Folia eucalypti with antibacterial drugs fosfomycin and ceftazidime. Visualization of morphometric changes and physical characteristics of the object of study was carried out using AFM. Results. Analysis of the experimental data obtained indicates that combinations of flavonoids with ceftazidime significantly reduced bacterial cell length by 5.5% (p < 0.05) for Dianthus and by 13.02% (p < 0.001) for Folia eucalypti. The combination of these phenolic extracts of Dianthus and Folia eucalypti with fosfomycin was characterized by significantly significant increases in length by 28.86% (p≤0.001), a decrease in width by 11.03% (p≤0.01) and height by 55.91% (p≤0.001) in the case of Dianthus, and a decrease in length by 5.5% (p≤0.05) and a height of 55.38% (p≤0.001) for Folia eucalypti. Thus, significantly significant changes in the morphometry of the bacterial cell were observed for all samples in comparison with the control. Conclusions: The data obtained confirm changes in the cell membrane of cells caused by the action of inhibitory components. The binding of anti-bacterial complexes with phospholipid groups changes the charge distribution across the membrane, disrupts internal membrane processes, inhibits the work of PSB, which causes a violation of peptidoglycan synthesis, and ultimately leads to a change in cell morphology.
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