Taherzadeh Sahar, Naeimifar Atefeh, Mehrabani Yeganeh Ehsan, Esmaili Zahra, Mahjoub Reza, Akbari Javar Hamid
Department of Pharmaceutics, Faculty of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran.
Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Adv Pharm Bull. 2021 Feb;11(2):301-310. doi: 10.34172/apb.2021.043. Epub 2020 Jun 20.
Propolis is a resinous material obtained by honeybees with many biological and pharmacological properties which can be used for treatment of various diseases. Current study aims to formulate and characterize propolis-loaded solid lipid nanoparticles (SLNs) carrier system. The prepared SLNs, composed of glyceryl monostearate (GMS), Soy lecithin, Tween 80 and polyethylene glycol 400 (PEG 400), were fabricated employing solvent emulsification-evaporation technique. In addition, the impact of several variables including concentration ratios of GMS/Soy lecithin and PEG 400/Tween 80 along with emulsification time were evaluated on the size, polydispersity index (PDI) and zeta potential of particles. SLN formulations were optimized using Box-Behnken design. The particles were freeze dried and morphologically studied by scanning electron microscopy (SEM). The in-vitro release profile of propolis entrapped in the optimized nanoparticles was investigated. The mean particle size, PDI, zeta potential, entrapment efficiency (EE) and loading efficiency (LE) of optimized propolis-loaded SLNs were found to be 122.6±22.36 nm, 0.28±0.06, -26.18±3.3 mV, 73.57±0.86% and 3.29±0.27%, respectively. SEM images exhibited nanoparticles to be non-aggregated and in spherical shape. The in-vitro release study showed prolonged release of propolis from nanoparticles. The results implied that the proposed way of SLN preparation could be considered as a proper method for production of propolis loaded colloidal carrier system.
蜂胶是蜜蜂采集的一种树脂状物质,具有多种生物学和药理学特性,可用于治疗各种疾病。当前的研究旨在制备和表征载蜂胶固体脂质纳米粒(SLN)载体系统。所制备的SLN由单硬脂酸甘油酯(GMS)、大豆卵磷脂、吐温80和聚乙二醇400(PEG 400)组成,采用溶剂乳化-蒸发技术制备。此外,评估了包括GMS/大豆卵磷脂浓度比、PEG 400/吐温80浓度比以及乳化时间等几个变量对颗粒大小、多分散指数(PDI)和zeta电位的影响。使用Box-Behnken设计对SLN制剂进行优化。将颗粒冷冻干燥,并通过扫描电子显微镜(SEM)进行形态学研究。研究了优化后的纳米粒中蜂胶的体外释放曲线。优化后的载蜂胶SLN的平均粒径、PDI、zeta电位、包封率(EE)和载药量(LE)分别为122.6±22.36 nm、0.28±0.36 nm、-26.18±3.3 mV、73.57±0.86%和3.29±0.27%。SEM图像显示纳米粒无聚集且呈球形。体外释放研究表明蜂胶从纳米粒中持续释放。结果表明,所提出的SLN制备方法可被视为生产载蜂胶胶体载体系统的合适方法。