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治疗性抗体向炎症结肠的位点选择性口服递送:一种叶酸接枝的有机/无机杂化纳米复合系统

Site-selective oral delivery of therapeutic antibodies to the inflamed colon a folic acid-grafted organic/inorganic hybrid nanocomposite system.

作者信息

Lee Sang Hoon, Song Jae Geun, Han Hyo-Kyung

机构信息

College of Pharmacy, Dongguk University-Seoul, Goyang 10326, South Korea.

出版信息

Acta Pharm Sin B. 2022 Nov;12(11):4249-4261. doi: 10.1016/j.apsb.2022.06.006. Epub 2022 Jun 10.

Abstract

This study aimed to develop a pH-responsive folic acid-grafted organic/inorganic hybrid nanocomposite system for site-selective oral delivery of therapeutic antibodies. A folic acid-grafted aminoclay (FA-AC) was prepared an sol‒gel method. Then, a drug-loaded nanocomplex was prepared the electrostatic interaction of FA-AC with infliximab (IFX), a model antibody, and coated with Eudragit® S100 (EFA-AC-IFX). FA-AC exhibited favorable profiles as a drug carrier including low cytotoxicity, good target selectivity, and capability to form a nanocomplex with negatively charged macromolecules. A pH-responsive FA-AC-based nanocomplex containing IFX (EFA-AC-IFX) was also obtained in a narrow size distribution with high entrapment efficiency (>87%). The conformational stability of IFX entrapped in EFA-AC-IFX was well maintained in the presence of proteolytic enzymes. EFA-AC-IFX exhibited pH-dependent drug release, minimizing premature drug release in gastric conditions and the upper intestine. Accordingly, oral administration of EFA-AC-IFX to colitis-induced mice was effective in alleviating the progression of ulcerative colitis, while oral IFX solution had no efficacy. These results suggest that a pH-responsive FA-AC-based nanocomposite system can be a new platform for the site-selective oral delivery of therapeutic antibodies.

摘要

本研究旨在开发一种用于治疗性抗体的位点选择性口服给药的pH响应型叶酸接枝有机/无机杂化纳米复合体系。通过溶胶-凝胶法制备了叶酸接枝氨基粘土(FA-AC)。然后,通过FA-AC与模型抗体英夫利昔单抗(IFX)的静电相互作用制备了载药纳米复合物,并用Eudragit® S100包衣(EFA-AC-IFX)。FA-AC作为药物载体表现出良好的特性,包括低细胞毒性、良好的靶向选择性以及与带负电荷大分子形成纳米复合物的能力。还获得了一种含IFX的基于pH响应型FA-AC的纳米复合物(EFA-AC-IFX),其粒径分布窄,包封率高(>87%)。在存在蛋白水解酶的情况下,EFA-AC-IFX中包封的IFX的构象稳定性得到了很好的维持。EFA-AC-IFX表现出pH依赖性药物释放,可将药物在胃部和上段肠道的过早释放降至最低。因此,给结肠炎诱导的小鼠口服EFA-AC-IFX可有效缓解溃疡性结肠炎的进展,而口服IFX溶液则无效。这些结果表明,基于pH响应型FA-AC的纳米复合体系可以成为治疗性抗体位点选择性口服给药的新平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83a5/9643170/1440d5b40d52/ga1.jpg

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