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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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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. |
format | Online Article Text |
id | pubmed-5620568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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