Effects of cefazolin-containing niosome nanoparticles against methicillin-resistant Staphylococcus aureus biofilm formed on chronic wounds. (26th February 2021)

• Record Type: Journal Article
• Authors: Zafari, Mahdi; Adibi, Mahsa; Chiani, Mohsen; Bolourchi, Negin; Barzi, Seyed Mahmoud; Shams Nosrati, Mohammad Sadegh; Bahari, Zeinab; Shirvani, Parisa; Noghabi, Kambiz Akbari; Ebadi, Mojgan; Rahimirad, Nazanin; Shafiei, Morvarid
• Is Part Of: Biomedical materials. Volume 16:Number 3(2021)
• Publication Date: 2021-02-26
• Subjects: cefazolin-loaded niosome nanoparticles -- methicillin-resistant S. aureus (MRSA) -- biofilm eradication -- chronic wound; Biomedical materials -- Periodicals; 610.28
• DOI: 10.1088/1748-605X/abc7f2
• Languages: English
• ISSNs: 1748-6041

Abstract

Abstract: The ability of biofilm formation in methicillin-resistant Staphylococcus aureus (MRSA) causes significant mortality and morbidity in wound infections. Nanoparticles because of the drug concentration increment at the point of contact of nanoparticles and bacteria, and slower release of the drug at the desired location are considered as proper tools to overcome the therapeutic problem of antimicrobial-resistant infections. This study was aimed to evaluate the anti-biofilm activity of cefazolin-loaded nanoparticles against MRSA isolates. The 27 clinical isolates of MRSA were collected from patients with pressure sores and diabetic ulcers referred to Loghman Hospital in Tehran—Iran. MRSA isolates were detected by polymerase chain reaction (PCR) and biochemical tests. Cefazolin-loaded niosome was synthesized using the thin-film hydration method and were characterized by zeta potential measurement and transmission electron microscopy (TEM). The round-shaped cefazolin-loaded niosomes had a diameter of 100 nm and a −63 mV zeta potential. The cefazolin-containing niosomes removed 1, 3, and 5 d old biofilms at the concentration of 128 µ g ml −1, 128 µ g ml −1, and 256 µ g ml −1, respectively. Histological results indicated that BALB/c mice receiving cefazolin-loaded niosomes were treated effectively faster than those treated by cefazolin or untreated group. In conclusion, the cefazolin-loaded niosome could be considered as a promising candidate for the treatment of biofilm-mediated infections of MRSA.