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用于非病毒口服基因治疗的质粒DNA纳米颗粒

Plasmid DNA Nanoparticles for Nonviral Oral Gene Therapy.

作者信息

Shahriar S M Shatil, An Jeong Man, Hasan Mohammad Nazmul, Surwase Sachin S, Kim Yeu-Chun, Lee Dong Yun, Cho Sungpil, Lee Yong-Kyu

机构信息

Department of Chemical and Biological Engineering, Korea National University of Transportation, Chungju-27469, Republic of Korea.

KB Biomed Inc., Chungju 27469, Republic of Korea.

出版信息

Nano Lett. 2021 Jun 9;21(11):4666-4675. doi: 10.1021/acs.nanolett.1c00832. Epub 2021 May 24.

DOI:10.1021/acs.nanolett.1c00832
PMID:34029475
Abstract

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 , , and 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.

摘要

在此,开发了一种受胆汁酸启发的三联锁口服基因递送平台,有助于保护治疗性基因免受胃肠道降解,通过胆汁酸特异性转运体实现选择性肠道蓄积,并通过肠肝循环系统运输质粒DNA纳米颗粒。这种非病毒口服基因递送纳米颗粒在相关研究中表现出优异的基因表达动力学。单次口服给药可使三种不同糖尿病小鼠模型的血糖正常水平维持长达7天,在糖尿病猴中维持14天。此外,优化后的剂型可将晚期糖尿病患者的非空腹血糖水平和糖化血红蛋白降低至正常范围,且在每周治疗一次、持续20周后,因食物摄取行为改变导致的体重增加减少。综上所述,目前的研究结果可改善糖尿病患者当前痛苦的治疗体验,从而提高他们的生活质量。

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