Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.
ACS Nano. 2022 Oct 25;16(10):16211-16220. doi: 10.1021/acsnano.2c05098. Epub 2022 Oct 6.
The delivery of macromolecular drugs 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 studies to characterize insulin release and assess the penetration capability of microinjectors and we measured the 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.
大分子药物在胃肠道(GI)中的递送具有挑战性,因为这些药物在肠道上皮细胞中的稳定性差且吸收不良。虽然渗透增强的药物递送方法可以提高低分子量药物的生物利用度,但有效递送至紧密的上皮细胞连接的高分子量药物仍然是一个巨大的挑战。在这里,我们描述了自主微注射器,这些微注射器部署在胃肠道中,然后有效地穿透胃肠道黏膜,将大分子药物胰岛素递送至全身循环。我们进行了研究以表征胰岛素的释放并评估微注射器的穿透能力,并在活体大鼠中测量了胰岛素的释放。我们发现,在腔道胃肠道内给药的微注射器可以将胰岛素经黏膜递送至全身循环,其水平与静脉内给予胰岛素相似。由于它们的体积小、尺寸和剂量的可调性、晶圆级制造以及并行、自主操作,我们预计这些微注射器将以安全的方式显著促进药物穿过胃肠道黏膜递送至全身循环。