Document Type: Research article
Herbal and Traditional Medicines Research Center, Kerman University of Medical Sciences, Kerman, Iran.
Department of Traditional pharmacy, School of persian Medicine, Kerman University of Medical Sciences, Kerman, Iran.
Pharmaceutics Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran
Herbal and traditional Medicines research Center, Faculty of Pharmacy, Kerman University of Medical Sciences, Kerman, Iran.
Physiology Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran
Department of Microbiology and Virology, School of Medicine, Kerman University of Medical Sciences, Kerman, Iran.
Herbal and Traditional Medicines Research Center- Kerman University of Medical sciences- Kerman- Iran
Traditionally, Myrtus communis (myrtle) has been used for treatment of several kinds of disorders. However, there are some factors, namely, low solubility and permeability, which restrict use of myrtle extract (ME) in medical applications. Regarding these limitations, the aim of the present study was to develop a new niosomal formulation to enhance ME stability and permeability.
Briefly, several niosomal formulations were prepared by non-ionic surfactants and cholesterol with different molar ratios. Afterward, size, entrapment efficiency (EE%), release and stability of niosomal myrtle extract (nME) were investigated. The effect of ME and nME on viability of 3T3 cells was evaluated using MTT assay. Antibacterial activity of ME and nME was also assessed against staphylococcus aureus, staphylococcus epidermidis, Escherichia coli, Micrococcus luteus, and Bacillus subtilis.
Sizes of niosomes were 5.3±0.3 to 15.9±2.2 µm with 4.1±0.3 to 26.9±1.7 mV zeta potential. The EE% of niosomes was varied from 45.4% to 93.4%. An in vitro release study on F5 formulation (Span60: Tween60: cholesterol (3:3:4 molar ratio)) revealed that about 36.9%, 38.5% and 26.7% of phytoconstituents were released within 12h from acetate cellulose membrane, 0.45 µm, regenerated cellulose membrane, 0.45 µm, and cellophane dialysis sack, 12000 Da, respectively. F5 formulation significantly showed lower toxicity on cells. It had higher antibacterial activity that has been shown by lower MICs and higher zone of inhibition compared to ME.
Overall, F5 formulation in the presence of 4% ME produced stable multi lamellar vesicles with optimal in-vitro release and EE%. This formulation also exhibited better antibacterial activity than ME.