Abstract

1A microwave (MW)‐assisted crosslinking process to prepare hydrogel‐forming microneedle (MN) arrays was evaluated. Conventionally, such MN arrays are prepared using processes that includes a thermal crosslinking step. Polymeric MN arrays were prepared using poly(methyl vinyl ether‐alt‐maleic acid) crosslinked by reaction with poly(ethylene glycol) over 24 h at 80 °C. Polymeric MN arrays were prepared to compare conventional process with the novel MW‐assisted crosslinking method. Infrared spectroscopy was used to evaluate the crosslinking degree, evaluating the area of the carbonyl peaks (2000–1500 cm−1). It was shown that, by using the MW‐assisted process, MN with a similar crosslinking degree to those prepared conventionally can be obtained in only 45 min. The effects of the crosslinking process on the properties of these materials were also evaluated. For this purpose swelling kinetics, mechanical characterisation, and insertion studies were performed. The results suggest that MN arrays prepared using the MW assisted process had equivalent properties to those prepared conventionally but can be produced 30 times faster. Finally, an in vitro caffeine permeation across excised porcine skin was performed using conventional and MW‐prepared MN arrays. The release profiles obtained can be considered equivalent, delivering in both cases 3000–3500 μg of caffeine after 24 h.

Highlights

  • IntroductionMicroneedle (MN) arrays are minimally-invasive devices composed of micron-size needles arranged in rows on a solid support

  • The copyright line of this paper was amended 14 January 2016.Microneedle (MN) arrays are minimally-invasive devices composed of micron-size needles arranged in rows on a solid support

  • These devices are able to painlessly by-pass outer skin barrier layer, the stratum corneum, the principal barrier to transdermal drug penetration. These devices can be used to deliver drugs to the deeper layers of the skin, from where they can be absorbed directly into the systemic circulation.[1]. These systems are attracting substantial interest due to their ability to transform the applicability of transdermal drug delivery.[2,3,4,5]

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Summary

Introduction

Microneedle (MN) arrays are minimally-invasive devices composed of micron-size needles arranged in rows on a solid support. These devices are able to painlessly by-pass outer skin barrier layer, the stratum corneum, the principal barrier to transdermal drug penetration. These devices can be used to deliver drugs to the deeper layers of the skin, from where they can be absorbed directly into the systemic circulation.[1] Currently, these systems are attracting substantial interest due to their ability to transform the applicability of transdermal drug delivery.[2,3,4,5]. Among polymeric MN, the hydrogel forming MN array system is of particular interest.[5,6,7,8,9]

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