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Detachable-dissolvable-microneedle as a potent subunit vaccine delivery device that requires no cold-chain
Although vaccine administration by microneedles has been demonstrated, delivery reliability issues have prevented their implementation. Through an ex vivo porcine skin experiment, we show visual evidence indicating that detachable dissolvable microneedles (DDMN) can deposit cargo into the dermis wit...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618702/ https://www.ncbi.nlm.nih.gov/pubmed/37920235 http://dx.doi.org/10.1016/j.jvacx.2023.100398 |
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author | Phoka, Theerapat Thanuthanakhun, Naruchit Visitchanakun, Peerapat Dueanphen, Narintorn Wanichwecharungruang, Nisha Leelahavanichkul, Asada Palaga, Tanapat Ruxrungtham, Kiat Wanichwecharungruang, Supason |
author_facet | Phoka, Theerapat Thanuthanakhun, Naruchit Visitchanakun, Peerapat Dueanphen, Narintorn Wanichwecharungruang, Nisha Leelahavanichkul, Asada Palaga, Tanapat Ruxrungtham, Kiat Wanichwecharungruang, Supason |
author_sort | Phoka, Theerapat |
collection | PubMed |
description | Although vaccine administration by microneedles has been demonstrated, delivery reliability issues have prevented their implementation. Through an ex vivo porcine skin experiment, we show visual evidence indicating that detachable dissolvable microneedles (DDMN) can deposit cargo into the dermis with insignificant loss of cargo to the stratum corneum. Using ovalbumin (OVA), a model antigen vaccine, as a cargo, the ex vivo experiments yielded a delivery efficiency of 86.08 ± 4.16 %. At room temperature, OVA could be stabilized for up to 35 days in DDMN made from hyaluronic acid and trehalose. The DDMN matrix could improve the denaturation temperature of the OVA from around 70–120 °C to over 150 °C, as demonstrated by differential scanning calorimetric analysis. In vivo delivery of OVA antigen into the mice's skin via DDMN elicited 10 times higher specific antibody responses compared to conventional intramuscular injection. We envision DDMN as an effective, precise dosing, intradermal vaccine delivery system that may require no cold-chain, offers a dose-sparing effect, and can be administered easily. |
format | Online Article Text |
id | pubmed-10618702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-106187022023-11-02 Detachable-dissolvable-microneedle as a potent subunit vaccine delivery device that requires no cold-chain Phoka, Theerapat Thanuthanakhun, Naruchit Visitchanakun, Peerapat Dueanphen, Narintorn Wanichwecharungruang, Nisha Leelahavanichkul, Asada Palaga, Tanapat Ruxrungtham, Kiat Wanichwecharungruang, Supason Vaccine X Regular paper Although vaccine administration by microneedles has been demonstrated, delivery reliability issues have prevented their implementation. Through an ex vivo porcine skin experiment, we show visual evidence indicating that detachable dissolvable microneedles (DDMN) can deposit cargo into the dermis with insignificant loss of cargo to the stratum corneum. Using ovalbumin (OVA), a model antigen vaccine, as a cargo, the ex vivo experiments yielded a delivery efficiency of 86.08 ± 4.16 %. At room temperature, OVA could be stabilized for up to 35 days in DDMN made from hyaluronic acid and trehalose. The DDMN matrix could improve the denaturation temperature of the OVA from around 70–120 °C to over 150 °C, as demonstrated by differential scanning calorimetric analysis. In vivo delivery of OVA antigen into the mice's skin via DDMN elicited 10 times higher specific antibody responses compared to conventional intramuscular injection. We envision DDMN as an effective, precise dosing, intradermal vaccine delivery system that may require no cold-chain, offers a dose-sparing effect, and can be administered easily. Elsevier 2023-10-16 /pmc/articles/PMC10618702/ /pubmed/37920235 http://dx.doi.org/10.1016/j.jvacx.2023.100398 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Regular paper Phoka, Theerapat Thanuthanakhun, Naruchit Visitchanakun, Peerapat Dueanphen, Narintorn Wanichwecharungruang, Nisha Leelahavanichkul, Asada Palaga, Tanapat Ruxrungtham, Kiat Wanichwecharungruang, Supason Detachable-dissolvable-microneedle as a potent subunit vaccine delivery device that requires no cold-chain |
title | Detachable-dissolvable-microneedle as a potent subunit vaccine delivery device that requires no cold-chain |
title_full | Detachable-dissolvable-microneedle as a potent subunit vaccine delivery device that requires no cold-chain |
title_fullStr | Detachable-dissolvable-microneedle as a potent subunit vaccine delivery device that requires no cold-chain |
title_full_unstemmed | Detachable-dissolvable-microneedle as a potent subunit vaccine delivery device that requires no cold-chain |
title_short | Detachable-dissolvable-microneedle as a potent subunit vaccine delivery device that requires no cold-chain |
title_sort | detachable-dissolvable-microneedle as a potent subunit vaccine delivery device that requires no cold-chain |
topic | Regular paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618702/ https://www.ncbi.nlm.nih.gov/pubmed/37920235 http://dx.doi.org/10.1016/j.jvacx.2023.100398 |
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