Antimicrobial activity of beta-lapachone encapsulated into liposomes against meticillin-resistant Staphylococcus aureus and Cryptococcus neoformans clinical strains

作者：Cavalcanti I M F; Pontes Neto J G; Kocerginsky P O; Bezerra Neto A M; Lima J L C; Lira Nogueira M C B; Maciel M A V; Neves R P; Pimentel M F; Santos Magalhaes N S^*

来源：Journal of Global Antimicrobial Resistance, 2015, 3(2): 103-108.

DOI：10.1016/j.jgar.2015.03.007

• beta-Lapachone
• Liposomes
• Antimicrobial activity
• Meticillin-resistant
• Staphylococcus aureus
• MRSA
• Cryptococcus neoformans

The aim of this study was to determine whether encapsulation of beta-lapachone (beta-lap) into liposomes interferes with its in vitro antimicrobial activity against meticillin-resistant Staphylococcus aureus (MRSA) and Cryptococcus neoformans clinical strains. Liposomes (beta-lap:lipo or beta-lap:HP beta-CD-lipo) were prepared using the hydration of thin lipid film method followed by sonication. The in vitro antimicrobial activities of beta-lap-loaded liposomes against MRSA and C. neoformans were evaluated using the microdilution method according to the Clinical and Laboratory Standards Institute (CLSI). The liposomes presented a mean particle size ranging from 88.7 +/- 1.5 nm to 112.4 +/- 1.9 nm with a polydispersity index ranging from 0.255 to 0.340, zeta potential from 0.26 +/- 0.01 mV to +0.25 +/- 0.05 mV and drug encapsulation efficiency from 97.4 +/- 0.3% to 98.9 +/- 0.4%. beta-Lap and beta-lap:HP beta-CD had minimum inhibitory concentrations (MICs) ranging from 2 mg/L to 4 mg/L, whereas the MICs of beta-lap-lipo or beta-lap:HP beta-CD-lipo ranged from 4 mg/L to 16 mg/L for the MRSA strains tested. beta-Lap and beta-lap:HP beta-CD were able to inhibit fungal growth [MIC = 2-8 mg/L and minimum fungicidal concentration (MFC) = 4-8 mg/L]. However, beta-lap-lipo and beta-lap:HP beta-CD-lipo were more efficient, with MICs and MFCs of <4 mg/L. These findings suggest that the liposomal formulations tested do not interfere significantly with beta-lap antibacterial activity against MRSA and improve its antifungal properties against C. neoformans.

• 出版日期2015-6