An ingestible self-orienting system for oral delivery of macromolecules

被引:323
作者
Abramson, Alex [1 ,2 ]
Caffarel-Salvador, Ester [1 ,2 ,3 ]
Khang, Minsoo [1 ,2 ]
Dellal, David [3 ]
Silverstein, David [1 ,2 ]
Gao, Yuan [1 ,2 ]
Frederiksen, Morten Revsgaard [4 ]
Vegge, Andreas [4 ]
Hubalek, Frantisek [4 ]
Water, Jorrit J. [4 ]
Friderichsen, Anders V. [4 ]
Fels, Johannes [4 ]
Kirk, Rikke Kaae [4 ]
Cleveland, Cody [1 ,2 ,4 ]
Collins, Joy [1 ,2 ]
Tamang, Siddartha [1 ,2 ]
Hayward, Alison [1 ,2 ,5 ]
Landh, Tomas [4 ]
Buckley, Stephen T. [4 ]
Roxhed, Niclas [1 ,2 ,6 ]
Rahbek, Ulrik [4 ]
Langer, Robert [1 ,2 ,3 ,7 ]
Traverso, Giovanni [1 ,2 ,8 ,9 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] MIT, Inst Med Engn & Sci, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[4] Novo Nordisk AS, Global Res Technol, Global Drug Discovery & Device R&D, Copenhagen, Denmark
[5] MIT, Div Comparat Med, Cambridge, MA 02139 USA
[6] KTH Royal Inst Technol, Dept Micro & Nanosyst, Stockholm, Sweden
[7] MIT, Media Lab, Cambridge, MA 02139 USA
[8] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[9] Harvard Med Sch, Brigham & Womens Hosp, Div Gastroenterol, Boston, MA 02115 USA
关键词
DRUG-DELIVERY; INSULIN; MICRONEEDLES; STOMACH; TABLETS;
D O I
10.1126/science.aau2277
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Biomacromolecules have transformed our capacity to effectively treat diseases; however, their rapid degradation and poor absorption in the gastrointestinal (GI) tract generally limit their administration to parenteral routes. An oral biologic delivery system must aid in both localization and permeation to achieve systemic drug uptake. Inspired by the leopard tortoise's ability to passively reorient, we developed an ingestible self-orienting millimeter-scale applicator (SOMA) that autonomously positions itself to engage with GI tissue. It then deploys milliposts fabricated from active pharmaceutical ingredients directly through the gastric mucosa while avoiding perforation. We conducted in vivo studies in rats and swine that support the applicator's safety and, using insulin as a model drug, demonstrated that the SOMA delivers active pharmaceutical ingredient plasma levels comparable to those achieved with subcutaneous millipost administration.
引用
收藏
页码:611 / +
页数:38
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