Department of Phytochemistry & Chemical Engineering, Medicinal Plants and Drugs Research Institute, Shahid Beheshti University, Tehran, Iran.
Department of Biology, Medicinal Plants and Drugs Research Institute, Shahid Beheshti University, Tehran, Iran.
Ultrason Sonochem. 2017 Mar;35(Pt A):415-421. doi: 10.1016/j.ultsonch.2016.10.020. Epub 2016 Oct 22.
Using ultrasonic technology, trans-cinnamaldehyde as a natural antibacterial compound was used to prepare nano size emulsions to increase its bioavailability and therefore bactericidal action. Nanoemulsions containing trans-cinnamaldehyde as an active agent and 1,8 cineol as co additive oil (Ostwald ripening inhibitor) were formulated using probe sonicator. Three different determining factors, namely time of sonication, surfactant to oil ratio and type of emulsifier (Tween 80 and Tween 20) were investigated to enhance the stability profile. In addition, the effect of changes in the particle size and emulsifier on the antibacterial activity against Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus were examined using agar dilution method. Then, the effect of optimized formulation on the membrane fluidity and cell constituent release, were investigated by analysis of membrane lipids using GC-MS and IR spectrometry, respectively. The data showed that a 15min sonication of the formulation containing Tween 80 as emulsifier with surfactant to oil ratio of 2:1 (w/w) resulted in a significant stability for 6months with considerably small particle size of 27.76±0.37nm. Furthermore, the nanoemulsion showed great antibacterial activity and could reduce the minimum inhibitory concentration (MIC) from 8 to 1mg/mL against E. coli and S. aureus, and from 16 to 2mg/mL against P. aeruginosa. Interestingly, E. coli's membrane fluidity increased dramatically after treatment with the optimum nanoemulsion (T804). This study revealed that nanoemulsion of trans-cinnamaldehyde and 1,8 cineol has substantial antibacterial activity against selected microorganisms.
采用超声波技术,将天然抗菌化合物反式肉桂醛制备成纳米乳液,以提高其生物利用度和杀菌作用。采用探头式超声仪,以 1,8-桉叶素为共加溶剂(奥斯特瓦尔德熟化抑制剂),配制含有反式肉桂醛作为活性成分的纳米乳液。考察了超声时间、表面活性剂与油的比例以及乳化剂(吐温 80 和吐温 20)的类型这三个不同的决定因素,以增强稳定性。此外,还通过琼脂稀释法考察了粒径和乳化剂的变化对大肠杆菌、铜绿假单胞菌和金黄色葡萄球菌的抗菌活性的影响。然后,通过 GC-MS 和 IR 光谱分别分析膜脂,考察优化配方对膜流动性和细胞成分释放的影响。数据表明,采用 Tween 80 作为乳化剂、表面活性剂与油的比例为 2:1(w/w)、超声 15min 的配方在 6 个月内具有显著的稳定性,粒径相当小,为 27.76±0.37nm。此外,纳米乳液表现出很强的抗菌活性,可以将最小抑菌浓度(MIC)从 8 降低至 1mg/mL 对大肠杆菌和金黄色葡萄球菌,从 16 降低至 2mg/mL 对铜绿假单胞菌。有趣的是,大肠杆菌的膜流动性在经最佳纳米乳液(T804)处理后显著增加。本研究表明,反式肉桂醛和 1,8-桉叶素的纳米乳液对选定的微生物具有显著的抗菌活性。