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Cyclodextrins as Oral Drug Carrier Molecular Devices: Origins, Reasons and In-vitro Model Applications

机译:环糊精作为口服药物载体的分子装置:起源,原因和体外模型的应用。

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摘要

Cyclodextrins are cyclic oligomers of glucose that can form water-soluble inclusion complexes with small molecules and portions of large compounds.These biocompatible, cyclic oligosaccharides do not elicit immune responses and have low toxicities in animals and humans.Cyclodextrins are used in pharmaceutical applications for numerous purposes, including improving the bioavailability of drugs.Current cyclodextrin-based therapeutics are described and possible future applications discussed with particular focus on oral drug administration.This article focuses on development of in vitro reliable and simple prototypes for oral drug delivery by combing chemical, structural and pharmacological knowledge available to date in order to create an optimal oral drug delivery system based on modified cyclodextrins.Practical in vitro model is also demonstrated.
机译:环糊精是葡萄糖的环状低聚物,可以与小分子和大分子的一部分形成水溶性包合物,这些生物相容性环状寡糖不会引起免疫反应,对动物和人类的毒性也很低。本文介绍了目前基于环糊精的治疗方法,并讨论了可能的未来应用,其中特别着重于口服药物的给药。本文着重于通过结合化学,结构方法开发口服药物体外可靠且简单的原型。以及迄今为止可获得的药理学知识,以基于修饰的环糊精创建最佳的口服药物递送系统。还证明了实用的体外模型。

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