Boury F, Marchais H, Benoit J P, Proust J E
Laboratoire de Pharmacie Galénique et Biophysique Pharmaceutique, Faculté de Pharmacie, Angers, France.
Biomaterials. 1997 Jan;18(2):125-36. doi: 10.1016/s0142-9612(96)00102-0.
This work constitutes the first attempt to characterize the wettability of poly(alpha-hydroxy acid) (PAHA) microspheres in situ, prepared according to a complex process involving emulsification, solvent evaporation, washing and freeze-drying. The analysis of the flotation profile of the microspheres has allowed us to determine both advancing and receding contact angles at the microsphere/air/water interface and furnished information on the organization of poly(vinyl alcohol) (PVA) and bovine serum albumin (BSA) at the surface of the PAHA coating. By the comparison of contact angles measured from model surfaces obtained by sampling pure PAHA, PVA, BSA and mixed PVA/PAHA monolayers on glass and poly(methyl methacrylate) (PMMA) substrates, it was concluded that the emulsifier (PVA or BSA) was strongly anchored to the surfaces of the microspheres. The use of BSA to formulate the microspheres from a single oil-in-water emulsion led to dry particles having a hydrophobic surface. The unfolding of the hydrophilic segments of the BSA embedded at the surface of the microspheres, following immersion in water, increased the wettability of the microspheres by water. The same qualitative results were obtained when PVA was used to stabilize single emulsions. On the other hand, microspheres formulated from a double water-in-oil-in-water emulsion displayed no modifications of their wettability when immersed in water. This can be explained by the absence of mobility of the hydrophilic segments of the emulsifier which are blocked in the surface or at the subsurface of the polymer matrix.
这项工作首次尝试对聚(α-羟基酸)(PAHA)微球的润湿性进行原位表征,该微球是根据包括乳化、溶剂蒸发、洗涤和冷冻干燥在内的复杂过程制备的。对微球浮选曲线的分析使我们能够确定微球/空气/水界面处的前进接触角和后退接触角,并提供了有关聚(乙烯醇)(PVA)和牛血清白蛋白(BSA)在PAHA涂层表面的组织信息。通过比较在玻璃和聚(甲基丙烯酸甲酯)(PMMA)基材上对纯PAHA、PVA、BSA以及混合PVA/PAHA单层进行采样获得的模型表面所测量的接触角,得出乳化剂(PVA或BSA)强烈锚定在微球表面的结论。使用BSA从单一水包油乳液制备微球会导致干燥颗粒具有疏水表面。微球表面嵌入的BSA亲水链段在浸入水中后展开,增加了微球对水的润湿性。当使用PVA稳定单一乳液时,也获得了相同的定性结果。另一方面,由双水包油包水乳液制备的微球浸入水中时其润湿性没有变化。这可以通过乳化剂的亲水链段在聚合物基质表面或次表面被阻断而缺乏流动性来解释。