Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra (FFUC) , Coimbra , Portugal.
CEB - Centre of Biological Engineering, University of Minho , Braga , Portugal.
Pharm Dev Technol. 2019 Nov;24(9):1181-1185. doi: 10.1080/10837450.2019.1647235. Epub 2019 Aug 8.
In this work, we report the development and optimization of solid lipid nanoparticles (SLN) production by a simple, fast, and cost-effective high shear homogenization process. A screening of several solid lipids (Compritol 888 ATO, Precirol ATO 5, Cetyl Palmitate, Dynasan 118, Imwitor 900K, Stearic acid) has been carried out in combination with Poloxamer 188 as the selected surfactant, based on the mean particle size and polydispersity index. The improvement of the physical stability of the SLN dispersions was achieved by the use of a cationic lipid (cetyl trimethylammonium bromide) reaching zeta potential values above +60 mV. Combining the optimized speed and time of shear, monodispersed SLN (PdI < 0.25) under the nanometer range could be produced.
在这项工作中,我们报告了通过简单、快速和具有成本效益的高剪切匀化工艺生产固体脂质纳米粒 (SLN) 的开发和优化。基于平均粒径和多分散指数,对几种固体脂质(Compritol 888 ATO、Precirol ATO 5、十六酸鲸蜡酯、Dynasan 118、Imwitor 900K、硬脂酸)与泊洛沙姆 188 进行了筛选,选择后者作为表面活性剂。通过使用阳离子脂质(十六烷基三甲基溴化铵)使 SLN 分散体的物理稳定性得到提高,达到了超过+60 mV 的 ζ 电位值。通过组合优化的剪切速度和时间,可以生产出单分散的纳米级 SLN(PdI < 0.25)。