Hydrogel‐Forming Microneedle Arrays for Enhanced Transdermal Drug Delivery

Ryan F. Donnelly(Queen's University Belfast), Thakur Raghu Raj Singh(Queen's University Belfast), Martin J. Garland(Queen's University Belfast), Katarzyna Migalska(Queen's University Belfast), Rita Majithiya(Queen's University Belfast), Cian M. McCrudden(Queen's University Belfast), Prashant Kole(Queen's University Belfast), Tuan Mazlelaa Tuan Mahmood(Queen's University Belfast), Helen O. McCarthy(Queen's University Belfast), A. David Woolfson(Queen's University Belfast)
Advanced Functional Materials
July 9, 2012
Cited by 686Open Access
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Abstract

Unique microneedle arrays prepared from crosslinked polymers, which contain no drug themselves, are described. They rapidly take up skin interstitial fluid upon skin insertion to form continuous, unblockable, hydrogel conduits from attached patch-type drug reservoirs to the dermal microcirculation. Importantly, such microneedles, which can be fabricated in a wide range of patch sizes and microneedle geometries, can be easily sterilized, resist hole closure while in place, and are removed completely intact from the skin. Delivery of macromolecules is no longer limited to what can be loaded into the microneedles themselves and transdermal drug delivery is now controlled by the crosslink density of the hydrogel system rather than the stratum corneum, while electrically modulated delivery is also a unique feature. This technology has the potential to overcome the limitations of conventional microneedle designs and greatly increase the range of the type of drug that is deliverable transdermally, with ensuing benefits for industry, healthcare providers and, ultimately, patients.


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