ABSTRACT
Drug loaded liposomes were prepared by a reverse
phase evaporation method using phospholipid (Soy lecithin),
cholesterol and stearylamine for having stable particles. The
characterization of the liposomes was carried out by estima-
tion of Azithromycin, estimation of encapsulation efficiency,
in vitro drug release, particles size, and stability of the lipo-
somes. The antibacterial action of the liposome solution was
assessed by disc diffusion method. The particle size of the
formulations ranged from 3.12 ± 5.429 to 3.60 ± 6.519 µm
and the entrapment efficiency ranged from 42.17 to 67.33
%. All the formulations released 62 to 75% drug at the end
of 8 hours of the study. The antibacterial action of the lipo-
somal formulation was compared to that of the pure drug
solution and it was found that the liposomal formulations
loaded with Azithromycin were able to exhibit comparable
antibacterial activity against Staphylococcus aureus in the
disc diffusion assay, as measured using the zone of inhibi-
tion.
Articles Details
NAMES:
ONLINE ISSN:2456-8244
Keywords: Azithromycin, liposomes, reverse phase evaporation, antibacterial, release
DOI:
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