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Built-In Active Microneedle Patch with Enhanced Autonomous Drug Delivery.

Authors :
Lopez-Ramirez MA
Soto F
Wang C
Rueda R
Shukla S
Silva-Lopez C
Kupor D
McBride DA
Pokorski JK
Nourhani A
Steinmetz NF
Shah NJ
Wang J
Source :
Advanced materials (Deerfield Beach, Fla.) [Adv Mater] 2020 Jan; Vol. 32 (1), pp. e1905740. Date of Electronic Publication: 2019 Nov 04.
Publication Year :
2020

Abstract

The use of microneedles has facilitated the painless localized delivery of drugs across the skin. However, their efficacy has been limited by slow diffusion of molecules and often requires external triggers. Herein, an autonomous and degradable, active microneedle delivery platform is introduced, employing magnesium microparticles loaded within the microneedle patch, as the built-in engine for deeper and faster intradermal payload delivery. The magnesium particles react with the interstitial fluid, leading to an explosive-like rapid production of H <subscript>2</subscript> bubbles, providing the necessary force to breach dermal barriers and enhance payload delivery. The release kinetics of active microneedles is evaluated in vitro by measuring the amount of IgG antibody (as a model drug) that passed through phantom tissue and a pigskin barrier. In vivo experiments using a B16F10 mouse melanoma model demonstrate that the active delivery of anti-CTLA-4 (a checkpoint inhibitor drug) results in greatly enhanced immune response and significantly longer survival. Moreover, spatially resolved zones of active and passive microneedles allow a combinatorial rapid burst response along with slow, sustained release, respectively. Such versatile and effective autonomous dynamic microneedle delivery technology offers considerable promise for a wide range of therapeutic applications, toward a greatly enhanced outcome, convenience, and cost.<br /> (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1521-4095
Volume :
32
Issue :
1
Database :
MEDLINE
Journal :
Advanced materials (Deerfield Beach, Fla.)
Publication Type :
Academic Journal
Accession number :
31682039
Full Text :
https://doi.org/10.1002/adma.201905740