Drug Res (Stuttg) 2014; 64(7): 348-352
DOI: 10.1055/s-0033-1358747
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Study of Antimicrobial Effects of Vancomycin Loaded PLGA Nanoparticles Against Enterococcus Clinical Isolates

F. Lotfipour
1   Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
2   Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran
,
S. Abdollahi
2   Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran
,
M. Jelvehgari
2   Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran
,
H. Valizadeh
2   Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran
,
M. Hassan
3   Faculty of Pharmacy, Zanjan University of Medical Sciences, Zanjan, Iran
,
M. Milani
4   School of Advanced Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
› Author Affiliations
Further Information

Publication History

received 29 July 2013

accepted 14 October 2013

Publication Date:
04 December 2013 (online)

Abstract

Researchers have demonstrated that antimicrobial agents in nanoparticle (NP) forms have better activities. Vancomycin (VCM), as a glycopeptide antibiotic with antimicrobial activity against gram positive bacteria, is poorly absorbed from the intestinal tract. Enterococcus is a genus of bacteria that became resistant to a wide range of antibiotics in last decades, and cause severe infections in hospitalized patients. This paper describes preparation of VCM – loaded poly (lactic-co-glycolic acid) (PLGA) NPs and compares the antimicrobial effects with drug solution against clinical Enterococcus isolates. VCM-loaded PLGA NPs were fabricated by W1/O/W2 solvent evaporation method. The comparison of obtained Minimum Inhibitory Concentration (MIC) values showed a significant decrease in the antimicrobial effect of VCM – loaded NPs. Results also indicated that the potency of the NPs against VCM resistant isolates of Enterococcus was less than VCM susceptible isolates. The reduced antimicrobial effect of formulated NPs in invitro condition is perhaps related to the strong electrostatic linkage between hydrophilic drug (VCM) and hydrophobic polymer (PLGA) that lead to the slow release of the antibiotic from polymeric NPs.