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Development of a thermostable microneedle patch for polio vaccination
The aim of this study was to develop a dissolving microneedle (MN) patch for administration of inactivated polio vaccine (IPV) with improved thermal stability when compared with conventional liquid IPV. Excipient screening showed that a combination of maltodextrin and D-sorbitol in histidine buffer...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328527/ https://www.ncbi.nlm.nih.gov/pubmed/30542944 http://dx.doi.org/10.1007/s13346-018-00608-9 |
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author | Kolluru, Chandana Gomaa, Yasmine Prausnitz, Mark R. |
author_facet | Kolluru, Chandana Gomaa, Yasmine Prausnitz, Mark R. |
author_sort | Kolluru, Chandana |
collection | PubMed |
description | The aim of this study was to develop a dissolving microneedle (MN) patch for administration of inactivated polio vaccine (IPV) with improved thermal stability when compared with conventional liquid IPV. Excipient screening showed that a combination of maltodextrin and D-sorbitol in histidine buffer best preserved IPV activity during MN patch fabrication and storage. As determined by D-antigen ELISA, all three IPV serotypes maintained > 70% activity after 2 months and > 50% activity after 1-year storage at 5 °C or 25 °C with desiccant. Storage at 40 °C yielded > 40% activity after 2 months and > 20% activity after 1 year. In contrast, commercial liquid IPV types 1 and 2 lost essentially all activity within 1 month at 40 °C and IPV type 3 had < 40% activity. Residual moisture content in MN patches measured by thermogravimetric analysis was 1.2–6.5%, depending on storage conditions. Glass transition temperature measured by differential scanning calorimetry, structural changes measured by X-ray diffraction, and molecular interactions measured by Fourier transform infrared spectroscopy showed changes in MN matrix properties, but they did not correlate with IPV activity changes during storage. We conclude that appropriately formulated MN patches can exhibit thermostability that could enable distribution of IPV with less reliance on cold chain storage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13346-018-00608-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6328527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-63285272019-01-25 Development of a thermostable microneedle patch for polio vaccination Kolluru, Chandana Gomaa, Yasmine Prausnitz, Mark R. Drug Deliv Transl Res Original Article The aim of this study was to develop a dissolving microneedle (MN) patch for administration of inactivated polio vaccine (IPV) with improved thermal stability when compared with conventional liquid IPV. Excipient screening showed that a combination of maltodextrin and D-sorbitol in histidine buffer best preserved IPV activity during MN patch fabrication and storage. As determined by D-antigen ELISA, all three IPV serotypes maintained > 70% activity after 2 months and > 50% activity after 1-year storage at 5 °C or 25 °C with desiccant. Storage at 40 °C yielded > 40% activity after 2 months and > 20% activity after 1 year. In contrast, commercial liquid IPV types 1 and 2 lost essentially all activity within 1 month at 40 °C and IPV type 3 had < 40% activity. Residual moisture content in MN patches measured by thermogravimetric analysis was 1.2–6.5%, depending on storage conditions. Glass transition temperature measured by differential scanning calorimetry, structural changes measured by X-ray diffraction, and molecular interactions measured by Fourier transform infrared spectroscopy showed changes in MN matrix properties, but they did not correlate with IPV activity changes during storage. We conclude that appropriately formulated MN patches can exhibit thermostability that could enable distribution of IPV with less reliance on cold chain storage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13346-018-00608-9) contains supplementary material, which is available to authorized users. Springer US 2018-12-12 2019 /pmc/articles/PMC6328527/ /pubmed/30542944 http://dx.doi.org/10.1007/s13346-018-00608-9 Text en © The Author(s) 2018 OpenAccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Kolluru, Chandana Gomaa, Yasmine Prausnitz, Mark R. Development of a thermostable microneedle patch for polio vaccination |
title | Development of a thermostable microneedle patch for polio vaccination |
title_full | Development of a thermostable microneedle patch for polio vaccination |
title_fullStr | Development of a thermostable microneedle patch for polio vaccination |
title_full_unstemmed | Development of a thermostable microneedle patch for polio vaccination |
title_short | Development of a thermostable microneedle patch for polio vaccination |
title_sort | development of a thermostable microneedle patch for polio vaccination |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328527/ https://www.ncbi.nlm.nih.gov/pubmed/30542944 http://dx.doi.org/10.1007/s13346-018-00608-9 |
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