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Polymer mixtures as colon targeted drug delivery systems

机译:聚合物混合物作为结肠靶向药物递送系统

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For the development of colon delivery systems (CDS) formulations have to be gastric resistant. The advantage of the CDS is the ability for a local treatment for colon diseases but also its systemic action. CDS can also increase the bioavailability of poorly water soluble drugs e.g. resveratrol, which can be degraded in the upper gastrointestinal tract or by the First-Pass-Effect. In this project the coating technique with different polymer mixtures containing Kollicoat M AE-30DP, Eudragit-NM, Eudragit-L, and Eudragit-NE was investigated. Resveratrol was used as a model drug and all formulations were coated with a polymer mixture in a small scale fluidized bed apparatus. Morphology, roughness and film thickness of the coated tablets were determined by a scanning electron microscope and a 3D light microscope. Drug amount was determined by UV-spectrometry. Release studies were performed in a dissolution apparatus type II. Kinetic profiles of drug release were demonstrated. Results exhibit the advantages of polymer mixtures for CDS in comparison with results of pure Kollicoat MAE-30DP which were published in one of our latest publications.
机译:为了开发结肠递送系统(CDS)制剂必须耐胃。 CDS的优点是临床疾病局部治疗的能力,而且是其系统性作用。 CD也可以增加水溶性差的药物的生物利用度,例如,较差的水溶性药物。白藜芦醇,可以在上胃肠道或通过第一通道效应降解。在该项目中,研究了含有Kollicoat M AE-30DP,Eudragit-NM,Eudragit -L和Eudragit-Ne的不同聚合物混合物的涂布技术。将白藜芦醇用作模型药物,并将所有制剂涂覆在小规模流化床设备中用聚合物混合物涂覆。通过扫描电子显微镜和3D光学显微镜测定涂覆片剂的形态,粗糙度和膜厚度。药物量通过UV光谱法测定。在溶解装置II型中进行释放研究。证明了药物释放的动力学谱。结果表明,与我们最新出版物之一发表的纯Kollicoat Mae-30dp的结果,表现出CDS的聚合物混合物的优点。

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