Bouchemal K, Briançon S, Perrier E, Fessi H
Laboratoire d'Automatique et de Génie des Procédés, UMR-CNRS 50 07 CPE Lyon, Université Claude Bernard Lyon 1, 43 Boulevard du 11, Novembre 1918, F-69622 Villeurbanne Cedex, France.
Int J Pharm. 2004 Aug 6;280(1-2):241-51. doi: 10.1016/j.ijpharm.2004.05.016.
Nano-emulsions consist of fine oil-in-water dispersions, having droplets covering the size range of 100-600 nm. In the present work, nano-emulsions were prepared using the spontaneous emulsification mechanism which occurs when an organic phase and an aqueous phase are mixed. The organic phase is an homogeneous solution of oil, lipophilic surfactant and water-miscible solvent, the aqueous phase consists on hydrophilic surfactant and water. An experimental study of nano-emulsion process optimisation based on the required size distribution was performed in relation with the type of oil, surfactant and the water-miscible solvent. The results showed that the composition of the initial organic phase was of great importance for the spontaneous emulsification process, and so, for the physico-chemical properties of the obtained emulsions. First, oil viscosity and HLB surfactants were changed, alpha-tocopherol, the most viscous oil, gave the smallest droplets size (171 +/- 2 nm), HLB required for the resulting oil-in-water emulsion was superior to 8. Second, the effect of water-solvent miscibility on the emulsification process was studied by decreasing acetone proportion in the organic phase. The solvent-acetone proportion leading to a fine nano-emulsion was fixed at 15/85% (v/v) with EtAc-acetone and 30/70% (v/v) with MEK-acetone mixture. To strength the choice of solvents, physical characteristics were compared, in particular, the auto-inflammation temperature and the flash point. This phase of emulsion optimisation represents an important step in the process of polymeric nanocapsules preparation using nanoprecipitation or interfacial polycondensation combined with spontaneous emulsification technique.
纳米乳液由精细的水包油分散体组成,其液滴尺寸范围为100 - 600纳米。在本研究中,纳米乳液采用自发乳化机制制备,即有机相和水相混合时发生的乳化过程。有机相是油、亲脂性表面活性剂和与水混溶的溶剂的均匀溶液,水相由亲水性表面活性剂和水组成。基于所需的粒径分布,针对油、表面活性剂和与水混溶的溶剂类型,开展了纳米乳液制备工艺优化的实验研究。结果表明,初始有机相的组成对于自发乳化过程至关重要,因此,对于所制备乳液的物理化学性质也至关重要。首先,改变油的粘度和表面活性剂的亲水亲油平衡值(HLB),α - 生育酚作为粘度最大的油,产生的液滴尺寸最小(171±2纳米),所形成的水包油乳液所需的HLB值大于8。其次,通过降低有机相中丙酮的比例,研究了水 - 溶剂混溶性对乳化过程的影响。对于乙酸乙酯 - 丙酮混合物,形成精细纳米乳液的溶剂 - 丙酮比例固定为15/85%(v/v);对于甲乙酮 - 丙酮混合物,该比例为30/70%(v/v)。为了强化溶剂的选择,比较了它们的物理特性,特别是自燃温度和闪点。乳液优化的这一阶段是使用纳米沉淀或界面缩聚结合自发乳化技术制备聚合物纳米胶囊过程中的重要一步。