Efficient oral insulin delivery enabled by transferrin-coated acid-resistant metal-organic framework nanoparticles

被引:85
|
作者
Zou, Jun-Jie [1 ]
Wei, Gaohui [1 ]
Xiong, Chuxiao [1 ]
Yu, Yunhao [1 ]
Li, Sihui [1 ]
Hu, Liefeng [1 ]
Ma, Shengqian [2 ]
Tian, Jian [1 ]
机构
[1] Wuhan Univ, Sch Pharmaceut Sci, Key Lab Combinatorial Biosynth & Drug Discovery M, Wuhan 430071, Peoples R China
[2] Univ North Texas, Dept Chem, Denton, TX 76201 USA
基金
中国国家自然科学基金;
关键词
LOADED NANOPARTICLES; DRUG-DELIVERY; RECEPTOR; EPITHELIUM; PROTEIN; DESIGN;
D O I
10.1126/sciadv.abm4677
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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-NH2) to encapsulate sufficient insulin and decorated the exterior with targeting proteins (transferrin) to realize highly efficient oral insulin delivery. The UiO-68-NH2 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.
引用
收藏
页数:12
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