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Administration of pilocarpine by microneedle patch as a novel method for cystic fibrosis sweat testing

The sweat test is the gold standard for the diagnosis of cystic fibrosis (CF). The test utilizes iontophoresis to administer pilocarpine to the skin to induce sweating for measurement of chloride concentration in sweat. However, the sweat test procedure needs to be conducted in an accredited lab wit...

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Autores principales: Li, Song, Hart, Kelsey, Norton, Natalie, Ryan, Clare A., Guglani, Lokesh, Prausnitz, Mark R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459588/
https://www.ncbi.nlm.nih.gov/pubmed/34589599
http://dx.doi.org/10.1002/btm2.10222
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author Li, Song
Hart, Kelsey
Norton, Natalie
Ryan, Clare A.
Guglani, Lokesh
Prausnitz, Mark R.
author_facet Li, Song
Hart, Kelsey
Norton, Natalie
Ryan, Clare A.
Guglani, Lokesh
Prausnitz, Mark R.
author_sort Li, Song
collection PubMed
description The sweat test is the gold standard for the diagnosis of cystic fibrosis (CF). The test utilizes iontophoresis to administer pilocarpine to the skin to induce sweating for measurement of chloride concentration in sweat. However, the sweat test procedure needs to be conducted in an accredited lab with dedicated instrumentation, and it can lead to inadequate sweat samples being collected in newborn babies and young children due to variable sweat production with pilocarpine iontophoresis. We tested the feasibility of using microneedle (MN) patches as an alternative to iontophoresis to administer pilocarpine to induce sweating. Pilocarpine‐loaded MN patches were developed. Both MN patches and iontophoresis were applied on horses to induce sweating. The sweat was collected to compare the sweat volume and chloride concentration. The patches contained an array of 100 MNs measuring 600 μm long that were made of water‐soluble materials encapsulating pilocarpine nitrate. When manually pressed to the skin, the MN patches delivered >0.5 mg/cm(2) pilocarpine, which was double that administered by iontophoresis. When administered to horses, MN patches generated the same volume of sweat when normalized to drug dose and more sweat when normalized to skin area compared to iontophoresis using a commercial device. Moreover, both MN patches and iontophoresis generated sweat with comparable chloride concentration. These results suggest that administration of pilocarpine by MN patches may provide a simpler and more‐accessible alternative to iontophoresis for performing a sweat test for the diagnosis of CF.
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spelling pubmed-84595882021-09-28 Administration of pilocarpine by microneedle patch as a novel method for cystic fibrosis sweat testing Li, Song Hart, Kelsey Norton, Natalie Ryan, Clare A. Guglani, Lokesh Prausnitz, Mark R. Bioeng Transl Med Research Articles The sweat test is the gold standard for the diagnosis of cystic fibrosis (CF). The test utilizes iontophoresis to administer pilocarpine to the skin to induce sweating for measurement of chloride concentration in sweat. However, the sweat test procedure needs to be conducted in an accredited lab with dedicated instrumentation, and it can lead to inadequate sweat samples being collected in newborn babies and young children due to variable sweat production with pilocarpine iontophoresis. We tested the feasibility of using microneedle (MN) patches as an alternative to iontophoresis to administer pilocarpine to induce sweating. Pilocarpine‐loaded MN patches were developed. Both MN patches and iontophoresis were applied on horses to induce sweating. The sweat was collected to compare the sweat volume and chloride concentration. The patches contained an array of 100 MNs measuring 600 μm long that were made of water‐soluble materials encapsulating pilocarpine nitrate. When manually pressed to the skin, the MN patches delivered >0.5 mg/cm(2) pilocarpine, which was double that administered by iontophoresis. When administered to horses, MN patches generated the same volume of sweat when normalized to drug dose and more sweat when normalized to skin area compared to iontophoresis using a commercial device. Moreover, both MN patches and iontophoresis generated sweat with comparable chloride concentration. These results suggest that administration of pilocarpine by MN patches may provide a simpler and more‐accessible alternative to iontophoresis for performing a sweat test for the diagnosis of CF. John Wiley & Sons, Inc. 2021-04-03 /pmc/articles/PMC8459588/ /pubmed/34589599 http://dx.doi.org/10.1002/btm2.10222 Text en © 2021 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Li, Song
Hart, Kelsey
Norton, Natalie
Ryan, Clare A.
Guglani, Lokesh
Prausnitz, Mark R.
Administration of pilocarpine by microneedle patch as a novel method for cystic fibrosis sweat testing
title Administration of pilocarpine by microneedle patch as a novel method for cystic fibrosis sweat testing
title_full Administration of pilocarpine by microneedle patch as a novel method for cystic fibrosis sweat testing
title_fullStr Administration of pilocarpine by microneedle patch as a novel method for cystic fibrosis sweat testing
title_full_unstemmed Administration of pilocarpine by microneedle patch as a novel method for cystic fibrosis sweat testing
title_short Administration of pilocarpine by microneedle patch as a novel method for cystic fibrosis sweat testing
title_sort administration of pilocarpine by microneedle patch as a novel method for cystic fibrosis sweat testing
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459588/
https://www.ncbi.nlm.nih.gov/pubmed/34589599
http://dx.doi.org/10.1002/btm2.10222
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