Literature DB >> 20727929

Optical coherence tomography is a valuable tool in the study of the effects of microneedle geometry on skin penetration characteristics and in-skin dissolution.

Ryan F Donnelly1, Martin J Garland, Desmond I J Morrow, Katarzyna Migalska, Thakur Raghu Raj Singh, Rita Majithiya, A David Woolfson.   

Abstract

In this study, we used optical coherence tomography (OCT) to extensively investigate, for the first time, the effect that microneedle (MN) geometry (MN height, and MN interspacing) and force of application have upon penetration characteristics of soluble poly(methylvinylether-co-maleic anhydride, PMVE/MA) MN arrays into neonatal porcine skin in vitro. The results from OCT investigations were then used to design optimal and suboptimal MN-based drug delivery systems and evaluate their drug delivery profiles cross full thickness and dermatomed neonatal porcine skin in vitro. It was found that increasing the force used for MN application resulted in a significant increase in the depth of penetration achieved within neonatal porcine skin. For example, MN of 600μm height penetrated to a depth of 330μm when inserted at a force of 4.4N/array, while the penetration increased significantly to a depth of 520μm, when the force of application was increased to 16.4N/array. At an application force of 11.0N/array it was found that, in each case, increasing MN height from 350 to 600μm to 900μm led to a significant increase in the depth of MN penetration achieved. Moreover, alteration of MN interspacing had no effect upon depth of penetration achieved, at a constant MN height and force of application. With respect to MN dissolution, an approximate 34% reduction in MN height occurred in the first 15min, with only 17% of the MN height remaining after a 3-hour period. Across both skin models, there was a significantly greater cumulative amount of theophylline delivered after 24h from an MN array of 900μm height (292.23±16.77μg), in comparison to an MN array of 350μm height (242.62±14.81μg) (p<0.001). Employing full thickness skin significantly reduced drug permeation in both cases. Importantly, this study has highlighted the effect that MN geometry and application force have upon the depth of penetration into skin. While it has been shown that MN height has an important role in the extent of drug delivered across neonatal porcine skin from a soluble MN array, further studies to evaluate the full significance of MN geometry on MN mediated drug delivery are now underway. The successful use of OCT in this study could prove to be a key development for polymeric MN research, accelerating their commercial exploitation.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20727929     DOI: 10.1016/j.jconrel.2010.08.008

Source DB:  PubMed          Journal:  J Control Release        ISSN: 0168-3659            Impact factor:   9.776


  63 in total

Review 1.  Microneedle-Mediated Vaccine Delivery to the Oral Mucosa.

Authors:  Rachel L Creighton; Kim A Woodrow
Journal:  Adv Healthc Mater       Date:  2018-12-10       Impact factor: 9.933

Review 2.  Microneedle characterisation: the need for universal acceptance criteria and GMP specifications when moving towards commercialisation.

Authors:  Rebecca E M Lutton; Jessica Moore; Eneko Larrañeta; Stephen Ligett; A David Woolfson; Ryan F Donnelly
Journal:  Drug Deliv Transl Res       Date:  2015-08       Impact factor: 4.617

3.  Hydrogel-forming microneedles increase in volume during swelling in skin, but skin barrier function recovery is unaffected.

Authors:  Ryan F Donnelly; Karen Mooney; Maelíosa T C McCrudden; Eva M Vicente-Pérez; Luc Belaid; Patricia González-Vázquez; James C McElnay; A David Woolfson
Journal:  J Pharm Sci       Date:  2014-03-14       Impact factor: 3.534

4.  Optimization of impedance spectroscopy techniques for measuring cutaneous micropore formation after microneedle treatment in an elderly population.

Authors:  Megan N Kelchen; Grant O Holdren; Matthew J Farley; M Bridget Zimmerman; Janet A Fairley; Nicole K Brogden
Journal:  Pharm Res       Date:  2014-06-20       Impact factor: 4.200

5.  Laser-engineered dissolving microneedle arrays for protein delivery: potential for enhanced intradermal vaccination.

Authors:  Maelíosa T C McCrudden; Barbara M Torrisi; Sharifah Al-Zahrani; Cian M McCrudden; Marija Zaric; Christopher J Scott; Adrien Kissenpfennig; Helen O McCarthy; Ryan F Donnelly
Journal:  J Pharm Pharmacol       Date:  2014-03-27       Impact factor: 3.765

6.  Impact-insertion applicator improves reliability of skin penetration by solid microneedle arrays.

Authors:  Koen van der Maaden; Emine Sekerdag; Wim Jiskoot; Joke Bouwstra
Journal:  AAPS J       Date:  2014-04-24       Impact factor: 4.009

7.  In vivo studies of transdermal nanoparticle delivery with microneedles using photoacoustic microscopy.

Authors:  Mohesh Moothanchery; Razina Z Seeni; Chenjie Xu; Manojit Pramanik
Journal:  Biomed Opt Express       Date:  2017-11-09       Impact factor: 3.732

8.  Hydrogel-forming microneedle arrays can be effectively inserted in skin by self-application: a pilot study centred on pharmacist intervention and a patient information leaflet.

Authors:  Ryan F Donnelly; Kurtis Moffatt; Ahlam Zaid Alkilani; Eva M Vicente-Pérez; Johanne Barry; Maelíosa T C McCrudden; A David Woolfson
Journal:  Pharm Res       Date:  2014-02-19       Impact factor: 4.200

9.  Label-Free, Longitudinal Visualization of PDT Response In Vitro with Optical Coherence Tomography.

Authors:  Yookyung Jung; Alexander J Nichols; Oliver J Klein; Emmanuel Roussakis; Conor L Evans
Journal:  Isr J Chem       Date:  2012-09-13       Impact factor: 3.333

10.  Flux of ionic dyes across microneedle-treated skin: effect of molecular characteristics.

Authors:  Yasmine A Gomaa; Martin J Garland; Fiona J McInnes; Ryan F Donnelly; Labiba K El-Khordagui; Clive G Wilson
Journal:  Int J Pharm       Date:  2012-08-30       Impact factor: 5.875

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