Zou Jun-Jie, Wei Gaohui, Xiong Chuxiao, Yu Yunhao, Li Sihui, Hu Liefeng, Ma Shengqian, Tian Jian
Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (MOE), School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071 P. R. China.
Department of Chemistry, University of North Texas, Denton, TX 76201, USA.
Sci Adv. 2022 Feb 25;8(8):eabm4677. doi: 10.1126/sciadv.abm4677. Epub 2022 Feb 23.
Oral protein delivery is considered a cutting-edge technology to improve patients' quality of life, offering superior patient compliance and convenience compared with injections. However, oral protein formulation has stagnated because of the instability and inefficient penetration of protein in the gastrointestinal tract. Here, we used acid-resistant metal-organic framework nanoparticles (UiO-68-NH) to encapsulate sufficient insulin and decorated the exterior with targeting proteins (transferrin) to realize highly efficient oral insulin delivery. The UiO-68-NH nanocarrier with proper pore size achieved high insulin loading while protecting insulin from acid and enzymatic degradation. Through receptor-mediated transcellular pathway, the transferrin-coated nanoparticles realized efficient transport across the intestinal epithelium and controlled insulin release under physiological conditions, leading to a notable hypoglycemic effect and a high oral bioavailability of 29.6%. Our work demonstrates that functional metal-organic framework nanoparticles can protect proteins from the gastric environment and overcome the intestinal barrier, thus providing the possibility for oral biomacromolecule delivery.
口服蛋白质给药被认为是一种改善患者生活质量的前沿技术,与注射给药相比,具有更高的患者依从性和便利性。然而,由于蛋白质在胃肠道中的不稳定性和渗透效率低下,口服蛋白质制剂的发展停滞不前。在此,我们使用耐酸金属有机框架纳米颗粒(UiO-68-NH)来封装足量的胰岛素,并在其外部修饰靶向蛋白(转铁蛋白),以实现高效的口服胰岛素递送。具有合适孔径的UiO-68-NH纳米载体实现了高胰岛素负载量,同时保护胰岛素免受酸和酶的降解。通过受体介导的跨细胞途径,转铁蛋白包被的纳米颗粒实现了跨肠上皮的有效转运,并在生理条件下控制胰岛素释放,从而产生显著的降血糖效果,口服生物利用度高达29.6%。我们的工作表明,功能性金属有机框架纳米颗粒可以保护蛋白质免受胃环境的影响并克服肠道屏障,从而为口服生物大分子递送提供了可能性。