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Inclusion of Pharmaceutical Compounds in Polymeric Membranes Produced by Supercritical Processing

机译:在通过超临界加工产生的聚合物膜中包含药物化合物

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Loaded polymeric membranes and aerogels have been prepared using, respectively, a supercritical fluid based phase inversion process in which COi acts as the nonsolvent and a supercritical drying process. We prepared polymeric membranes and gels of PVDF-HFP loaded with a model drug, amoxicillin, using two different processes. To produce loaded membranes we prepared a dispersion of the drug in the organic solution formed by polymer and solvent; instead, gels have been prepared adding ethanol to the casting solution and cooling it at -20°C for 30 min. Loaded membranes and aerogels, produced at various drug loadings, were characterized by SEM, to study the morphology and cells size, by DSC to analyze drug-polymer interactions in the membrane and by microanalysis (EDX) to examine the drug distribution in the polymeric matrix. Moreover, drug release rate analysis were performed to observe the different release behaviors. The results are very different depending on supercritical process used: phase inversion or gel drying. In the first case we obtained cellular structure with non homogeneous drug distribution and consequently a fast drug release; when we prepare aerogels, instead, the structure results more homogeneous, with no dmg concentration gradient along the section.
机译:分别制备了加载的聚合物膜和气凝胶,其基于超临界流体的相倒置方法,其中COI用作非溶剂和超临界干燥过程。我们使用两种不同的方法制备了用模型药物,含有模型药物,阿莫西林的PVDF-HFP的聚合物膜和凝胶。为了产生负载膜,我们制备了药物在聚合物和溶剂形成的有机溶液中的分散体;相反,已经制备凝胶向浇铸溶液中加入乙醇并在-20℃下冷却30分钟。在各种药物载体中产生的负载膜和气凝胶,其特征在于SEM,以研究形态和细胞的大小,通过DSC分析膜中的药物 - 聚合物相互作用和通过微分析(EDX)来检查聚合物基质中的药物分布。此外,进行药物释放速率分析以观察不同的释放行为。结果取决于所用超临界方法:相倒置或凝胶干燥。在第一种情况下,我们在具有非均相药物分布的细胞结构中获得了细胞结构,因此快速的药物释放;当我们准备气凝胶时,结构会更加均匀,沿着该截面没有DMG浓度梯度。

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