遗传增强
体内
糖尿病
基因传递
胆汁酸
离体
化学
药理学
基因
口服
血红蛋白
基因表达
生物
医学
体外
生物化学
内分泌学
生物技术
作者
S. M. Shatil Shahriar,Jeong Man An,Mohammad Nazmul Hasan,Sachin S. Surwase,Yeu‐Chun Kim,Dong Yun Lee,Sungpil Cho,Yong-Kyu Lee
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-05-24
卷期号:21 (11): 4666-4675
被引量:20
标识
DOI:10.1021/acs.nanolett.1c00832
摘要
Herein, a bile acid-inspired triple padlock oral gene delivery platform is developed, facilitating the protection of the therapeutic gene from gastrointestinal degradation, selective intestinal accumulation through a bile acid-specific transporter, and transportation of pDNA NPs through the enterohepatic recycling system. This nonviral oral gene delivery nanoparticle exhibits excellent gene expression kinetics in in vitro, in vivo, and ex vivo studies. A single oral dose leads to maintaining normoglycemia for up to 7 days in three different diabetes mouse models and 14 days in diabetic monkeys. Also, the optimized dosage form can reduce nonfast blood glucose levels and hemoglobin A1C within a normal range from the last stage diabetes conditions with a reduction of weight gain from changes of food uptake behavior after treatment once weekly for 20 weeks. Taken together, the current findings could improve the current painful treatment experience of diabetics and thus improve their quality of life.
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