Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX, USA.
Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX, USA; Institute of Biomaterials, Drug Delivery, and Regenerative Medicine, University of Texas at Austin, Austin, TX, USA.
J Control Release. 2023 Dec;364:216-226. doi: 10.1016/j.jconrel.2023.10.020. Epub 2023 Oct 31.
While a number of enteric coatings and pH-sensitive oral delivery vehicles have been developed, they lack the ability to sufficiently protect proteins from proteolytic degradation once released from the carrier. In this work, we show that H-bonded, pH-sensitive poly(methacrylic acid-grafted ethylene glycol) glycol (henceforth designated as P(MAA-g-EG) gels) exhibit great promise as protein carriers, as they utilize poly(ethylene glycol) (PEG) chains to promote mucoadhesion in the small intestine, increasing the chances that the drug is released within the villus of the absorptive intestinal wall. Importantly, PEG was also conjugated to the B29-lysine (LysB29) position of insulin in order to protect the drug from proteolytic degradation once released in the small intestine and adhere the drug to the intestinal epithelium through improved mucoadhesion. PEG-conjugated (PEGylated) molecules were found to actively participate in the carrier loading and release mechanism, with the drug conjugate hydrogen bonding to the MAA while in the collapsed state and subsequently repulse the drug above the polymer's isoelectric point. This effect was enhanced through the evaluation of PEG graft density within the carrier. Cellular transport and changes in transepithelial resistance caused by the PEGylated insulin (PI) in the presence of P(MAA-g-EG) microparticles were analyzed using a 1:1 co-culture of human colon adenocarcinoma (Caco-2) and: the mucus-secreting human colon carcinoma cell(HT-29-MTX). Finally, the in vivo absorption of insulin was measured in Sprague-Dawley rats to ensure that the PEGylated insulin conjugates are biologically active, as well as to compare the bioavailability to control insulin. Collectively, these results lead toward the development of a novel system for improved insulin delivery, with improved stability of insulin through PEGylation.
尽管已经开发出了许多肠溶性涂层和 pH 敏感的口服递药载体,但它们缺乏在从载体中释放后充分保护蛋白质免受蛋白水解降解的能力。在这项工作中,我们表明,氢键合的 pH 敏感的聚(甲基丙烯酸接枝乙二醇)凝胶(以下简称 P(MAA-g-EG)凝胶)作为蛋白质载体具有很大的应用潜力,因为它们利用聚乙二醇(PEG)链在小肠中促进黏膜黏附,从而增加药物在吸收性肠壁绒毛中释放的机会。重要的是,PEG 还被共轭到胰岛素的 B29-赖氨酸(LysB29)位置,以保护药物在小肠中释放后免受蛋白水解降解,并通过改善黏膜黏附将药物附着在肠上皮上。发现 PEG 共轭(PEG 化)分子积极参与载体加载和释放机制,药物与 MAA 发生氢键相互作用,而在塌陷状态下,药物随后在聚合物等电点以上排斥药物。通过评估载体中的 PEG 接枝密度,可以增强这种效应。通过 1:1 共培养人结肠腺癌细胞(Caco-2)和分泌黏液的人结肠癌细胞(HT-29-MTX),分析了 P(MAA-g-EG)微粒中 PEG 化胰岛素(PI)存在时对细胞转运和跨上皮电阻的影响。最后,在 Sprague-Dawley 大鼠中测量胰岛素的体内吸收,以确保 PEG 化胰岛素缀合物具有生物活性,并比较其与对照胰岛素的生物利用度。总之,这些结果为改善胰岛素递送开发了一种新的系统,通过 PEG 化提高了胰岛素的稳定性。