Title of article :
In-vitro and In-vivo Evaluation of Silymarin Nanoliposomes against Isolated Methicillin-resistant Staphylococcus aureus
Author/Authors :
Faezizadeh, Zohreh Department of Laboratory Sciences - Borujerd Branch - Islamic Azad University, Borujerd , Gharib, Amir Department of Laboratory Sciences - Borujerd Branch - Islamic Azad University, Borujerd , Godarzee, Masoud Department of Biology - Borujerd Branch - Islamic Azad University, Borujerd
Pages :
7
From page :
627
To page :
633
Abstract :
Staphylococcus aureus is an opportunistic pathogen and remains a common cause of burn wound infections. Different studies have shown that entrapment of plant-derived compounds into liposomes could increase their anti-Staphylococcus aureus activity. Silymarin is the bioactive extract from the known plant Silybum marianum L. The objective of this study was to evaluate efficacy of silymarin in free and nanoliposomal forms against isolated methicillinresistant Staphylococcus aureus (MRSA) strain. Silymarin-loaded nanoliposomes were prepared by extrusion method. The minimum inhibitory concentrations (MICs) of silymarin in free and nanoliposomal forms against MRSA were determined by broth dilution method. The killing rate of free and nanoliposomal forms of silymarin were analyzed. Ultimately, invivo therapeutic efficacy of nanoliposomes in burned mice infected by isolated MRSA was examined. The MICs of free and nanoliposomal forms of silymarin against isolated strain were 500 and 125 mg/L, respectively. The killing rate of silymarin-loaded nanoliposomes was higher than those of free silymarin. Topically treatment by silymarin in free and nanoliposomal forms resulted in almost 20 and 100% survival rates, respectively. The results suggest that silymarinloaded nanoliposomes may provide a basis for future treatment of MRSA infections.
Keywords :
Silymarin , Nanoliposome , Methicillin-resistant Staphylococcus aureus , Killing rate , In-vitro , In-vivo
Journal title :
Astroparticle Physics
Serial Year :
2015
Record number :
2416997
Link To Document :
بازگشت