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Peroral peptide drug delivery using superporous hydrogel (SPH) and SPh composite polymers: drug release and enzyme inhibition studies

机译:使用超多孔水凝胶(SPH)和SPh复合聚合物的经口肽药物递送:药物释放和酶抑制研究

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In the last two decades numerous attempts have been made by many scientists to overcome the prolbem of peroral absorption of peptide and protein drugs. Different approaches have been proposed, such as using mucoadhesive polymers, applying penetration enhancers to interact iwth the gut membrane, using enzyme inhibitors and/or substances to open the tight junctions in order to enhance the poor peptide absorption and low bioavailability. In this study, a novel drug delivery system for intestinal absorption of peptide and protein drugs is designed with the use of superporous hydrogel (SPH) and SPH composites polymers. One of the outstanding characteristics of this new delivery system is its mechanism of action. These polymers are able to swell very rapidly by absorption of gut fluids, so they can mechancially attach to the intestinal wall and keep the dosage form at the site of action for a specific period of time in which the drug will be released and absorbed. In this report, the capacity of these polymers for enzyme inactivation is also described.
机译:在过去的二十年中,许多科学家进行了许多尝试来克服经口吸收肽和蛋白质药物的问题。已经提出了不同的方法,例如使用粘膜粘附性聚合物,施加渗透促进剂以与肠膜相互作用,使用酶抑制剂和/或物质打开紧密连接以增强不良的肽吸收和低生物利用度。在这项研究中,使用超多孔水凝胶(SPH)和SPH复合材料聚合物设计了一种新型的肽和蛋白质药物肠道吸收药物递送系统。这种新的传递系统的突出特点之一是其作用机理。这些聚合物能够通过吸收肠液而迅速膨胀,因此它们可以机械地附着在肠壁上,并使剂型在特定的作用时间段内保持释放并吸收药物的作用部位。在该报告中,还描述了这些聚合物的酶失活能力。

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