胰岛素
药物输送
全身循环
胃肠道
生物利用度
药理学
药品
体内
医学
生物
内科学
材料科学
纳米技术
生物技术
作者
Arijit Ghosh,Wangqu Liu,Ling Li,Gayatri Pahapale,Si Young Choi,Liyi Xu,Qi Huang,Ruili Zhang,Zijian Zhong,Florin M. Selaru,David H. Gracias
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-10-06
卷期号:16 (10): 16211-16220
被引量:15
标识
DOI:10.1021/acsnano.2c05098
摘要
The delivery of macromolecular drugs via the gastrointestinal (GI) tract is challenging as these drugs display low stability as well as poor absorption across the intestinal epithelium. While permeation-enhancing drug delivery methods can increase the bioavailability of low molecular weight drugs, the effective delivery of high molecular weight drugs across the tight epithelial cell junctions remains a formidable challenge. Here, we describe autonomous microinjectors that are deployed in the GI tract, then efficiently penetrate the GI mucosa to deliver a macromolecular drug, insulin, to the systemic circulation. We performed in vitro studies to characterize insulin release and assess the penetration capability of microinjectors and we measured the in vivo release of insulin in live rats. We found that the microinjectors administered within the luminal GI tract could deliver insulin transmucosally to the systemic circulation at levels similar to those with intravenously administered insulin. Due to their small size, tunability in sizing and dosing, wafer-scale fabrication, and parallel, autonomous operation, we anticipate that these microinjectors will significantly advance drug delivery across the GI tract mucosa to the systemic circulation in a safe manner.
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