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首页> 外文期刊>Journal of Polymers and the Environment >Solvent-Cast Polymeric Films from Pectin and Eudragit® NE 30D for Transdermal Drug Delivery Systems
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Solvent-Cast Polymeric Films from Pectin and Eudragit® NE 30D for Transdermal Drug Delivery Systems

机译:来自果胶和Eudragit®NE30D的溶剂浇注的聚合物薄膜用于透皮药物递送系统

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In this study, solvent-cast polymeric films containing ionic liquid lidocaine/aspirin for transdermal patches were developed. Solvent-cast polymeric films were prepared from two polymers, pectin and Eudragit(R) NE 30D, by drying the polymeric solution in a hot air oven at 70 +/- 3 degrees C for 10 h. Glycerin was used as a plasticizer. Lidocaine and aspirin were prepared in ionic liquid form and loaded into the patches. The physicomechanical properties of the films were characterized by texture analysis, differential scanning calorimetry, thermogravimetric analysis, and X-ray diffraction. A scanning electron microscope was used to photograph the surfaces of solvent-cast polymeric films. Eudragit(R) NE 30D significantly decreased the toughness and rigidity of the films. The transdermal patches were in the amorphous state, and their thermal properties were not changed from blank polymeric films. The surfaces of transdermal patches were rougher than blank polymeric films and revealed the distribution of the drug. Eudragit(R) NE 30D significantly decreased the trends of entrapment efficiency and in vitro release of lidocaine and aspirin drugs. The kinetic release observed in vitro fitted to Higuchi's model rather than zero and first order models, indicating that a diffusion mechanism governed the release of the drug from the patch. Thus, the solvent-cast polymeric films from two polymers, pectin and Eudragit(R) NE 30D, are suitable for transdermal patches loaded with ionic liquid lidocaine/aspirin.
机译:在该研究中,开发了含有离子液体利多卡因/阿司匹林用于透皮贴剂的溶剂铸型聚合物膜。通过将聚合物溶液在70 +/- 3℃下干燥10小时,从两种聚合物,果胶和Eudragit(R)Ne 30d制备溶剂铸型聚合物膜。甘油用作增塑剂。利多卡因和阿司匹林以离子液体形式制备并装入贴剂中。通过纹理分析,差示扫描量热法,热重分析和X射线衍射的特征在于膜的物理机械性质。扫描电子显微镜用于拍摄溶剂铸造聚合物膜的表面。 EUDRAGIT(R)NE 30D显着降低了薄膜的韧性和刚性。透皮贴剂在无定形状态下,它们的热性能没有从空白聚合物膜改变。透皮贴剂的表面比空白聚合物膜更粗糙,并揭示了药物的分布。 Eudragit(R)NE 30D显着降低了Lid Caine和Aspirin药物的夹带效率和体外释放的趋势。在体外观察到Higuchi的模型而不是零和一阶模型的动力学释放,表明扩散机制控制了来自贴剂的药物的释放。因此,来自两个聚合物,果胶和eudragit(R)Ne 30d的溶剂浇铸聚合物膜适用于负载离子液体利多卡因/阿司匹林的透皮贴剂。

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