針を使わずインスリンを送達する爆発型カプセルを開発(These ‘Exploding’ Capsules Can Deliver Insulin Without a Needle)

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2025-07-08 ジョージア工科大学(Georgia Tech)

針を使わずインスリンを送達する爆発型カプセルを開発(These ‘Exploding’ Capsules Can Deliver Insulin Without a Needle)

ジョージア工科大学の研究者らが、インスリンなどの注射薬を経口投与可能にする「爆発カプセル」を開発した。このカプセルは小腸内で小規模な圧力“爆発”を起こし、薬剤を血流に直接送り込むことで、胃腸のバリアを突破する。電池や可動部品は不要で、従来の注射に代わる低侵襲・簡便な投薬手段として注目されている。動物実験では血糖降下効果が注射と同等で、GLP-1薬(オゼンピックなど)や抗体医薬にも応用可能。成果は『Journal of Controlled Release』誌に掲載された。

<関連情報>

自己加圧経口カプセルによる消化管経由での生物製剤の高速送達 High-velocity delivery of biologics via the gastrointestinal tract by self-pressurized oral capsules

Joshua I. Palacios, Amy J. Wood-Yang, Nicholas Klavohn, Nick Friesenhahn, Nisha Raman, Nusaiba Baker, Grant Ashby, Mark R. Prausnitz
Journal of Controlled Release  Available online: 18 June 2025
DOI:https://doi.org/10.1016/j.jconrel.2025.113963

Highlights

  • High-velocity delivery enabled transport of biologics across small intestine mucosa.
  • Oral, self-pressurized aerosol (OSPRAE) hard gelatin capsules were designed.
  • OSPRAE capsules made of biocompatible excipients had no electric or mechanical parts.
  • OSPRAE capsules enabled insulin delivery in vivo with improved bioavailability.
  • Only superficial and microscopic tissue damage was observed.

Abstract

Biologic drugs have transformed medicine, but are limited by their need for administration by injection. To enable oral delivery of biologics, we propose convective force as a physical method to overcome the barriers of the gastrointestinal tract (GIT). We designed oral capsules that self-pressurize in the GIT, mechanically fail at a specific pressure (100–170 kPa), and eject lyophilized drug with sufficient velocity to penetrate the mucosal barrier. This oral, self-pressurized aerosol (OSPRAE) was produced by a coated gelatin capsule filled with pressure-generating effervescent excipients (sodium bicarbonate, citric acid) and drug in a biodegradable polymer chamber (poly(lactic acid)). After initial optimization in vitro, OSPRAE allowed for insulin delivery to surgically exposed intestinal mucosa in vivo with similar pharmacokinetics and pharmacodynamics to subcutaneous injection in rats, despite lower bioavailability. Histological analysis showed only superficial damage to the intestinal epithelium that was highly localized to the microscopic area of impact. Future studies should administer OSPRAE orally to larger animals and, ultimately, to humans. The OSPRAE capsule offers a novel method to increase delivery of biologics across the intestinal mucosa using convective force, which contrasts with prior approaches involving chemical penetration enhancers and electromechanical devices.

医療・健康
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