Methods Monostearin solid lipid nanoparticles was prepared by solvent diffusion method in aqueous system.
方法用水性溶剂扩散法，制备得到甘油单硬脂酸酯固体脂质纳米粒。
A modified free - volume diffusion model for binary aqueous mixtures in pervaporation was developed on the basis of free -volume diffusion theory.
在自由体积扩散理论的基础上，提出了渗透蒸发过程中二元水溶液在聚合物膜中扩散的修正自由体积模型。
Retinoic acid (RA) nanoparticle suspensions with different concentrations were prepared by solvent-diffusion method in aqueous and freeze-drying.
采用溶剂分散法制备了不同药物质量浓度的维甲酸纳米颗粒混悬剂，并对其进行了冷冻干燥；
Dissolution Capacity of Hydrophobic Drugs in Aqueous Solution--Solubility and Diffusion Gibbs Free Energy;
这种的溶解度可能与非水合物的溶解度有明显的不同。
Dissolution Capacity of Hydrophobic Drugs in Aqueous Solution--Solubility and Diffusion Gibbs Free Energy;
这种的溶解度可能与非水合物的溶解度有明显的不同。
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