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Development of Novel Faster-Dissolving Microneedle Patches for Transcutaneous Vaccine Delivery

Microneedle (MN) patches are promising for transcutaneous vaccination because they enable vaccine antigens to physically penetrate the stratum corneum via low-invasive skin puncturing, and to be effectively delivered to antigen-presenting cells in the skin. In second-generation MN patches, the disso...

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Autores principales: Ono, Akihiko, Ito, Sayami, Sakagami, Shun, Asada, Hideo, Saito, Mio, Quan, Ying-Shu, Kamiyama, Fumio, Hirobe, Sachiko, Okada, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620568/
https://www.ncbi.nlm.nih.gov/pubmed/28771172
http://dx.doi.org/10.3390/pharmaceutics9030027
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author Ono, Akihiko
Ito, Sayami
Sakagami, Shun
Asada, Hideo
Saito, Mio
Quan, Ying-Shu
Kamiyama, Fumio
Hirobe, Sachiko
Okada, Naoki
author_facet Ono, Akihiko
Ito, Sayami
Sakagami, Shun
Asada, Hideo
Saito, Mio
Quan, Ying-Shu
Kamiyama, Fumio
Hirobe, Sachiko
Okada, Naoki
author_sort Ono, Akihiko
collection PubMed
description Microneedle (MN) patches are promising for transcutaneous vaccination because they enable vaccine antigens to physically penetrate the stratum corneum via low-invasive skin puncturing, and to be effectively delivered to antigen-presenting cells in the skin. In second-generation MN patches, the dissolving MNs release the loaded vaccine antigen into the skin. To shorten skin application time for clinical practice, this study aims to develop novel faster-dissolving MNs. We designed two types of MNs made from a single thickening agent, carboxymethylcellulose (CMC) or hyaluronan (HN). Both CMC-MN and HN-MN completely dissolved in rat skin after a 5-min application. In pre-clinical studies, both MNs could demonstrably increase antigen-specific IgG levels after vaccination and prolong antigen deposition compared with conventional injections, and deliver antigens into resected human dermal tissue. In clinical research, we demonstrated that both MNs could reliably and safely puncture human skin without any significant skin irritation from transepidermal water loss measurements and ICDRG (International Contact Dermatitis Research Group) evaluation results.
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spelling pubmed-56205682017-10-03 Development of Novel Faster-Dissolving Microneedle Patches for Transcutaneous Vaccine Delivery Ono, Akihiko Ito, Sayami Sakagami, Shun Asada, Hideo Saito, Mio Quan, Ying-Shu Kamiyama, Fumio Hirobe, Sachiko Okada, Naoki Pharmaceutics Article Microneedle (MN) patches are promising for transcutaneous vaccination because they enable vaccine antigens to physically penetrate the stratum corneum via low-invasive skin puncturing, and to be effectively delivered to antigen-presenting cells in the skin. In second-generation MN patches, the dissolving MNs release the loaded vaccine antigen into the skin. To shorten skin application time for clinical practice, this study aims to develop novel faster-dissolving MNs. We designed two types of MNs made from a single thickening agent, carboxymethylcellulose (CMC) or hyaluronan (HN). Both CMC-MN and HN-MN completely dissolved in rat skin after a 5-min application. In pre-clinical studies, both MNs could demonstrably increase antigen-specific IgG levels after vaccination and prolong antigen deposition compared with conventional injections, and deliver antigens into resected human dermal tissue. In clinical research, we demonstrated that both MNs could reliably and safely puncture human skin without any significant skin irritation from transepidermal water loss measurements and ICDRG (International Contact Dermatitis Research Group) evaluation results. MDPI 2017-08-03 /pmc/articles/PMC5620568/ /pubmed/28771172 http://dx.doi.org/10.3390/pharmaceutics9030027 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ono, Akihiko
Ito, Sayami
Sakagami, Shun
Asada, Hideo
Saito, Mio
Quan, Ying-Shu
Kamiyama, Fumio
Hirobe, Sachiko
Okada, Naoki
Development of Novel Faster-Dissolving Microneedle Patches for Transcutaneous Vaccine Delivery
title Development of Novel Faster-Dissolving Microneedle Patches for Transcutaneous Vaccine Delivery
title_full Development of Novel Faster-Dissolving Microneedle Patches for Transcutaneous Vaccine Delivery
title_fullStr Development of Novel Faster-Dissolving Microneedle Patches for Transcutaneous Vaccine Delivery
title_full_unstemmed Development of Novel Faster-Dissolving Microneedle Patches for Transcutaneous Vaccine Delivery
title_short Development of Novel Faster-Dissolving Microneedle Patches for Transcutaneous Vaccine Delivery
title_sort development of novel faster-dissolving microneedle patches for transcutaneous vaccine delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620568/
https://www.ncbi.nlm.nih.gov/pubmed/28771172
http://dx.doi.org/10.3390/pharmaceutics9030027
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