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IgG 功能化聚合物纳米粒用于口服胰岛素给药。

IgG functionalized polymeric nanoparticles for oral insulin administration.

机构信息

Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS 90610-000, Brazil; Universidade de Coimbra, Faculdade de Farmácia, Coimbra, Portugal.

Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS 90610-000, Brazil; Departamento de Química Orgânica, Instituto de Química, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS 90650-001, Brazil.

出版信息

Int J Pharm. 2022 Jun 25;622:121829. doi: 10.1016/j.ijpharm.2022.121829. Epub 2022 May 14.

Abstract

The oral route is the best way to administer a drug; however, fitting peptide drugs in this route is a major challenge. In insulin cases, less than 0.5% of the administered dose achieves systemic circulation. Oral delivery by nanoparticles can increase insulin permeability across the intestinal epithelium while maintaining its structure and activity until release in the gut. This system can be improved to increase permeability across intestinal cells through active delivery. This study aimed to improve a nanoparticle formulation by promoting functionalization of its surface with immunoglobulin G to increase its absorption by intestinal epithelium. The characterization of formulations showed an adequate size and a good entrapment efficiency. Functionalized nanoparticles led to a desirable increase in insulin release time. Differential scanning calorimetry, infrared spectroscopy and paper chromatography proved the interactions of nanoparticle components. With immunoglobulin G, the nanoparticle size was slightly increased, which did not show aggregate formation. The developed functionalized nanoparticle formulation proved to be adequate to carry insulin and potentially increase its internalization by epithelial gut cells, being a promising alternative to the existing formulations for orally administered low-absorption peptides.

摘要

口服是给药的最佳途径;然而,将肽类药物制成适合口服的剂型是一个重大挑战。在胰岛素的情况下,只有不到 0.5%的给药剂量能达到全身循环。通过纳米粒进行口服给药可以增加胰岛素在肠道上皮细胞中的通透性,同时保持其结构和活性,直到在肠道中释放。通过主动递送来改善该系统可以增加穿过肠细胞的通透性。本研究旨在通过促进免疫球蛋白 G 对纳米粒表面的功能化来提高其对肠道上皮细胞的吸收,从而改进纳米粒的配方。制剂的特性分析表明其具有合适的粒径和良好的包封效率。功能化纳米粒可使胰岛素释放时间得到理想的延长。差示扫描量热法、红外光谱和纸层析证明了纳米粒成分之间的相互作用。免疫球蛋白 G 的加入使纳米粒的粒径略有增加,但没有出现聚集形成。所开发的功能化纳米粒制剂被证明可以携带胰岛素,并有可能增加其被肠道上皮细胞内化,这是现有低吸收肽类口服制剂的一种有前途的替代方案。

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