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DNA-based Bi-layered effervescent ejecting microneedle (BEE MN) for glucose-responsive insulin delivery.

Yoonbin Ji1, Kyung A Kim1, Iksoo Jang1

  • 1Department of Chemical Engineering, University of Seoul, 163 Seoulsiripdaero, Dongdaemun-gu, Seoul 02504, Republic of Korea. jblee@uos.ac.kr.

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This study introduces a novel bi-layered effervescent ejecting microneedle (BEE MN) system that uses CO2 gas for self-propulsion. This innovation enhances transdermal drug delivery, offering efficient, on-demand insulin administration for diabetes management.

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Area of Science:

  • Biomaterials Science
  • Drug Delivery Systems
  • Nanotechnology

Background:

  • Conventional injections face limitations in drug loading and release for chronic diseases.
  • Microneedle technology offers minimally invasive alternatives but requires enhanced delivery mechanisms.

Purpose of the Study:

  • To develop a novel bi-layered effervescent ejecting microneedle (BEE MN) system for enhanced transdermal drug delivery.
  • To engineer a glucose-responsive system for precise, on-demand insulin administration.

Main Methods:

  • Designed a dual-stage microneedle with a glucose-responsive DNA reservoir and an effervescent matrix for CO2 generation.
  • Utilized rolling circle amplification (RCA) to create insulin-binding aptamer structures.
  • Evaluated drug penetration, retention, and glucose-triggered release in vitro.

Main Results:

  • The BEE MN system demonstrated CO2-powered self-propulsion, improving drug delivery into the dermal layer.
  • Engineered DNA reservoirs enabled high-density aptamer structures for controlled insulin release.
  • Achieved efficient, glucose-responsive insulin release under hyperglycemic conditions.

Conclusions:

  • The CO2-powered, self-propulsive microneedle system offers enhanced transdermal drug delivery capabilities.
  • This technology presents a promising platform for next-generation smart insulin delivery systems.
  • The BEE MN system overcomes limitations of traditional microneedles for efficient, on-demand drug administration.