2024 : 11 : 21
Majid Tafrihi

Majid Tafrihi

Academic rank: Associate Professor
ORCID:
Education: PhD.
ScopusId:
HIndex:
Faculty: Science
Address: Department of Molecular and Cell Biology, Faculty of Basic Sciences, University of Mazandaran, Babolsar, Mazandaran, Iran, Postal code: 4741695447
Phone: 01135305252

Research

Title
Antibacterial effect of cerium oxide nanoparticle against Pseudomonas aeruginosa
Type
JournalPaper
Keywords
Cerium oxide nanoparticles, Nanofiber, Antibiotic resistance, Pseudomonas aeruginosa, Gene expression, Cytotoxicity, Clinical isolate
Year
2021
Journal BMC BIOTECHNOLOGY
DOI
Researchers Khosro Zamani ، Noushin Allah‑Bakhshi ، Faezeh Akhavan ، Mahdieh Yousefi ، Rezvan Golmoradi ، Horacio Bach ، Shabnam Razavi ، Gholamreza Irajian ، Mahyar Gerami ، Ali Pakdin‑Parizi ، Majid Tafrihi ، Fatemeh Ramezani ، Moazzameh Ramezani

Abstract

Background: Antibiotics have been widely used for the treatment of bacterial infections for decades. However, the rapid emergence of antibiotic‑resistant bacteria has created many problems with a heavy burden for the medical community. Therefore, the use of nanoparticles as an alternative for antibacterial activity has been explored. In this context, metal nanoparticles have demonstrated broad‑spectrum antimicrobial activity. This study investigated the antimicrobial activity of naked cerium oxide nanoparticles dispersed in aqueous solution (CNPs) and surface‑stabi‑ lized using Pseudomonas aeruginosa as a bacterial model. Methods: Gelatin‑polycaprolactone nanofibers containing CNPs (Scaffold@CNPs) were synthesized, and their effect on P. aeruginosa was investigated. The minimum inhibitory and bactericidal concentrations of the nanoparticls were determined in an ATCC reference strain and a clinical isolate strain. To determine whether the exposure to the nano‑ composites might change the expression of antibiotic resistance, the expression of the genes shv, kpc, and imp was also investigated. Moreover, the cytotoxicity of the CNPs was assessed on fibroblast using flow cytometry. Results: Minimum bactericidal concentrations for the ATCC and the clinical isolate of 50 µg/mL and 200 µg/mL were measured, respectively, when the CNPs were used. In the case of the Scaffold@CNPs, the bactericidal effect was 50 µg/mL and 100 µg/mL for the ATCC and clinical isolate, respectively. Interestingly, the exposure to the Scaffold@ CNPs significantly decreased the expression of the genes shv, kpc, and imp. Conclusions: A concentration of CNPs and scaffold@CNPs higher than 50 μg/mL can be used to inhibit the growth of P. aeruginosa. The fact that the scaffold@CNPs significantly reduced the expression of resistance genes, it has the potential to be used for medical applications such as wound dressings.