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Motion Capture Quantification of User Variation in Topical Microparticle Application

Motion capture has the potential to shed light on topical drug delivery application. This approach holds promise both as a training tool, and for the development of skin technology, but first, this approach requires validation. Elongated microparticles (EMP) are a physical delivery enhancement techn...

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Autores principales: Snoswell, Aaron J., Yamada, Miko, Kirby, Giles T. S., Singh, Surya P. N., Prow, Tarl W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7508043/
https://www.ncbi.nlm.nih.gov/pubmed/33013374
http://dx.doi.org/10.3389/fphar.2020.01343
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author Snoswell, Aaron J.
Yamada, Miko
Kirby, Giles T. S.
Singh, Surya P. N.
Prow, Tarl W.
author_facet Snoswell, Aaron J.
Yamada, Miko
Kirby, Giles T. S.
Singh, Surya P. N.
Prow, Tarl W.
author_sort Snoswell, Aaron J.
collection PubMed
description Motion capture has the potential to shed light on topical drug delivery application. This approach holds promise both as a training tool, and for the development of skin technology, but first, this approach requires validation. Elongated microparticles (EMP) are a physical delivery enhancement technology that relies on a user working in the microparticles using a textured applicator. We used this approach to test the hypothesis that motion capture data can be used to characterize the topical application process. Motion capture was used to record participants while applying a mixture of EMP and sodium fluorescein to ex-vivo porcine skin samples. Treated skin was assessed using reflectance confocal and fluorescence microscopy. Image analysis was used to quantify the microparticle density and the presence of a fluorescent drug surrogate, sodium fluorescein. A strong correlation was present between applicator motion and microparticle and drug delivery profiles. There were quantitative and qualitative differences in the intra- and inter- user application methods that went beyond the level of training. Frequency and velocity of the applicator motion were key factors that correlated with EMP density. Our quantitative analysis of an experimental dermatological device supports the hypothesis that self-application may benefit from some form of digital monitoring or training with feedback. Our conclusion is that the integration of motion capture into experimental dermatological research offers an improved and quantifiable perspective that could be broadly useful with respect to topical applications, and with respect to the instruction provided to patients and clinicians.
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spelling pubmed-75080432020-10-02 Motion Capture Quantification of User Variation in Topical Microparticle Application Snoswell, Aaron J. Yamada, Miko Kirby, Giles T. S. Singh, Surya P. N. Prow, Tarl W. Front Pharmacol Pharmacology Motion capture has the potential to shed light on topical drug delivery application. This approach holds promise both as a training tool, and for the development of skin technology, but first, this approach requires validation. Elongated microparticles (EMP) are a physical delivery enhancement technology that relies on a user working in the microparticles using a textured applicator. We used this approach to test the hypothesis that motion capture data can be used to characterize the topical application process. Motion capture was used to record participants while applying a mixture of EMP and sodium fluorescein to ex-vivo porcine skin samples. Treated skin was assessed using reflectance confocal and fluorescence microscopy. Image analysis was used to quantify the microparticle density and the presence of a fluorescent drug surrogate, sodium fluorescein. A strong correlation was present between applicator motion and microparticle and drug delivery profiles. There were quantitative and qualitative differences in the intra- and inter- user application methods that went beyond the level of training. Frequency and velocity of the applicator motion were key factors that correlated with EMP density. Our quantitative analysis of an experimental dermatological device supports the hypothesis that self-application may benefit from some form of digital monitoring or training with feedback. Our conclusion is that the integration of motion capture into experimental dermatological research offers an improved and quantifiable perspective that could be broadly useful with respect to topical applications, and with respect to the instruction provided to patients and clinicians. Frontiers Media S.A. 2020-09-08 /pmc/articles/PMC7508043/ /pubmed/33013374 http://dx.doi.org/10.3389/fphar.2020.01343 Text en Copyright © 2020 Snoswell, Yamada, Kirby, Singh and Prow http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Snoswell, Aaron J.
Yamada, Miko
Kirby, Giles T. S.
Singh, Surya P. N.
Prow, Tarl W.
Motion Capture Quantification of User Variation in Topical Microparticle Application
title Motion Capture Quantification of User Variation in Topical Microparticle Application
title_full Motion Capture Quantification of User Variation in Topical Microparticle Application
title_fullStr Motion Capture Quantification of User Variation in Topical Microparticle Application
title_full_unstemmed Motion Capture Quantification of User Variation in Topical Microparticle Application
title_short Motion Capture Quantification of User Variation in Topical Microparticle Application
title_sort motion capture quantification of user variation in topical microparticle application
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7508043/
https://www.ncbi.nlm.nih.gov/pubmed/33013374
http://dx.doi.org/10.3389/fphar.2020.01343
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