Institut Galien Paris-Sud, CNRS UMR 8612, Univ. Paris-Sud, Université Paris-Saclay, Faculté de Pharmacie , 5 rue J.B. Clément , F-92296 Châtenay-Malabry , France.
Laboratoire Structures, Propriétés et Modélisation des Solides (SPMS) UMR CNRS 8580, CentraleSupélec, Université Paris-Saclay , 3 Rue Joliot Curie , 91190 Gif-sur-Yvette , France.
Langmuir. 2018 Nov 20;34(46):13935-13945. doi: 10.1021/acs.langmuir.8b02558. Epub 2018 Nov 5.
Pickering emulsions were formulated using biodegradable and biocompatible poly(lactic- co-glycolic acid) (PLGA) nanoparticles (NPs) prepared without surfactants or any other polymer than PLGA. A pharmaceutical and cosmetic oil (Miglyol) was chosen as the oil phase at a ratio of 10% w/w. These emulsions were then compared with emulsions using the same oil but formulated with well-described PLGA-poly(vinyl alcohol) (PVA) NPs, i.e., with PVA as NP stabilizers. Strikingly, the emulsions demonstrated very different structures at macroscopic, microscopic, and interfacial scales, depending on the type of NPs used. Indeed, the emulsion layer was significantly thicker when using PLGA NPs rather than PLGA-PVA NPs. This was attributed to the formation and coexistence of multiple water-in-oil-in-water (W/O/W) and simple oil-in-water (O/W) droplets, using a single step of emulsification, whereas simple O/W emulsions were obtained with PLGA-PVA NPs. The latter NPs were more hydrophilic than bare PLGA NPs because of the presence of PVA at their surface. Moreover, PLGA NPs only slightly lowered the oil/water interfacial tension whereas the decrease was more pronounced with PLGA-PVA NPs. The PVA chains at the PLGA-PVA NP surface could probably partially desorb from the NPs and adsorb at the interface, inducing the interfacial tension decrease. Finally, independent of their composition, NPs were adsorbed at the oil/water interface without influencing its rheological behavior, possibly due to their mobility at their interface. This work has direct implications in the formulation of Pickering emulsions and stresses the paramount influence of the physicochemical nature of the NP surface into the stabilization of these systems.
使用可生物降解和生物相容的聚(乳酸-共- 羟基乙酸)(PLGA)纳米粒子(NPs)制备了 Pickering 乳液,这些 NPs 是在没有表面活性剂或除 PLGA 以外的任何聚合物的情况下制备的。选择一种药物和化妆品油(Miglyol)作为油相,比例为 10%w/w。然后将这些乳液与使用相同油但用经过良好描述的 PLGA-聚乙烯醇(PVA)NPs 制备的乳液进行比较,即 PVA 作为 NP 稳定剂。引人注目的是,根据所使用的 NPs 类型,乳液在宏观、微观和界面尺度上表现出非常不同的结构。实际上,与使用 PLGA-PVA NPs 相比,使用 PLGA NPs 时乳液层明显更厚。这归因于在单个乳化步骤中形成并共存多个水包油包水(W/O/W)和简单的油包水(O/W)液滴,而使用 PLGA-PVA NPs 则获得简单的 O/W 乳液。后者的 NPs 比裸 PLGA NPs 更亲水,因为其表面存在 PVA。此外,PLGA NPs 仅略微降低油/水界面张力,而 PLGA-PVA NPs 的降低更为明显。PLGA-PVA NP 表面的 PVA 链可能部分从 NPs 中解吸并吸附在界面上,导致界面张力降低。最后,无论其组成如何,NP 都被吸附在油/水界面上,而不会影响其流变行为,这可能是由于它们在界面上的迁移性。这项工作对 Pickering 乳液的配方具有直接影响,并强调了 NP 表面的物理化学性质对这些系统稳定化的至关重要的影响。