Boonme P, Krauel K, Graf A, Rades T, Junyaprasert V B
Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok.
Pharmazie. 2006 Nov;61(11):927-32.
The aim of this work was to determine the type and microstructure of microemulsion samples formed in IPP/water/AerosolOT:1-butanol (2:1) systems as a case study for the investigation of microemulsions. The concentration of the surfactant/cosurfactant mixture was kept constant while the ratio of water to oil was varied. Several techniques were used to investigate the types and phase transitions of the microemulsion formulations. The experimental methods used included visual observation cross-polarized light microscopy (PLM) appearance, conductivity, viscosity, cryo-field emission scanning electron microscopy (cryo-FESEM), differential scanning calorimetry (DSC), nuclear magnetic resonance (NMR), and fluorescence resonance energy transfer (FRET). Taken together, the results of the various techniques imply that the systems investigated are undergoing two transitions as a function of water concentration. Between 10-15%w/w of water, the systems change from headgroup hydrated surfactant solutions in oil (or possibly very small reversed micellar systems) to w/o microemulsions. These systems then change to o/w microemulsions between 25-30%w/w of water. The transitions however, appear to be gradual, as for example the DSC data indicates a transition between 15-20%w/w of water. Furthermore, for some methods the changes observed were very weak, and only with supportive data of other techniques can the phase behaviour of the microemulsion systems be interpreted with confidence. Interestingly, no indication of the presence of a bicontinuous intermediate microstructure was found. Liquid crystal formation was detected in samples containing 55%w/w of water.
本研究的目的是确定在IPP/水/气溶胶OT:1-丁醇(2:1)体系中形成的微乳液样品的类型和微观结构,以此作为微乳液研究的一个案例。表面活性剂/助表面活性剂混合物的浓度保持恒定,而水与油的比例则有所变化。采用了多种技术来研究微乳液配方的类型和相变。所使用的实验方法包括目视观察、偏光显微镜(PLM)外观、电导率、粘度、低温场发射扫描电子显微镜(cryo-FESEM)、差示扫描量热法(DSC)、核磁共振(NMR)和荧光共振能量转移(FRET)。综合来看,各种技术的结果表明,所研究的体系随着水浓度的变化经历了两个转变。在水含量为10-15%w/w之间,体系从油相中头基水合的表面活性剂溶液(或可能是非常小的反胶束体系)转变为油包水微乳液。然后,这些体系在水含量为25-30%w/w之间转变为水包油微乳液。然而,这些转变似乎是渐进的,例如DSC数据表明在水含量为15-20%w/w之间存在转变。此外,对于某些方法,观察到的变化非常微弱,只有结合其他技术的支持数据,才能自信地解释微乳液体系的相行为。有趣的是,没有发现存在双连续中间微观结构的迹象。在水含量为55%w/w的样品中检测到了液晶形成。