利用多孔材料口服给药结肠的扩散模型。

Austin Evers, Symone L M Alexander
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引用次数: 0

摘要

口服给药是患者的首选,因为易于给药,微创的程序,和整体简单。然而,由于胃肠道的生理屏障,传统的口服药物可能导致治疗无效和不良副作用。正因为如此,由聚合物、多孔材料合成的结肠特异性药物递送载体被设计用来控制药物向结肠的释放。具体来说,这些多孔基质包括水凝胶、微凝胶/微颗粒和纳米颗粒药物输送系统。此外,还研究了这些制剂的生存能力和将药物输送到结肠的有效性。本文综述了扩散和药物释放的扩散模型,以及基质材料的选择如何决定药物释放的可能性。我们的目标是为识别、应用和推进药物扩散到结肠的模型提供资源,以帮助指导针对肠道病变的药物递送载体的实验设计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diffusion Models for Oral Drug Delivery to the Colon Using Porous Materials.

Oral administration of drugs is patient-preferred due to ease of administration, less invasive procedures, and overall simplicity. However, traditional oral administration of drugs can lead to ineffective treatment and adverse side effects due to the physiological barriers of the gastrointestinal tract. Because of this, colon-specific drug delivery vehicles synthesized from polymeric, porous materials are being designed to control drug release to the colon. Specifically, these porous matrices include hydrogels, microgels/microparticles, and nanoparticle drug delivery systems. Furthermore, these formulations have been studied on their survivability and efficacy in delivery of the drugs to the colon. This review paper is focused on diffusion models for diffusion and drug release and how the choice of matrix material determines what drug release profiles are possible. Our goal is to provide a resource for identifying, applying, and advancing models for drug diffusion to the colon to help guide experimental design of drug delivery vehicles for intestinal pathologies.

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