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Identifying a stable bulk dmLT adjuvant formulation at a clinically relevant concentration

Double mutant heat-labile toxin (dmLT) is a novel vaccine adjuvant under development with several different vaccine candidates. Studies using existing dmLT adjuvant stocks require significant dilution to achieve a clinically relevant dose. This dilution leads to wastage of the adjuvant. This manuscr...

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Detalles Bibliográficos
Autores principales: Estrada, Marcus R., Bzami, Anan, Norton, Elizabeth B., White, Jessica A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9932622/
https://www.ncbi.nlm.nih.gov/pubmed/36658044
http://dx.doi.org/10.1016/j.vaccine.2023.01.005
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author Estrada, Marcus R.
Bzami, Anan
Norton, Elizabeth B.
White, Jessica A.
author_facet Estrada, Marcus R.
Bzami, Anan
Norton, Elizabeth B.
White, Jessica A.
author_sort Estrada, Marcus R.
collection PubMed
description Double mutant heat-labile toxin (dmLT) is a novel vaccine adjuvant under development with several different vaccine candidates. Studies using existing dmLT adjuvant stocks require significant dilution to achieve a clinically relevant dose. This dilution leads to wastage of the adjuvant. This manuscript describes a limited formulation study to improve the stability of bulk dmLT at a more clinically relevant concentration (20 µg/mL) with minimal changes to the existing bulk dmLT formulation. In vitro methods were used to evaluate dmLT stability after lyophilization and short-term accelerated stability studies. The addition of the excipient polysorbate 80 (PS80) at 0.05 % to the existing dmLT formulation was identified as the lead modification that provided improved stability of the lyophilized dmLT at 20 µg/mL through 4 weeks at 40 °C.
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spelling pubmed-99326222023-02-17 Identifying a stable bulk dmLT adjuvant formulation at a clinically relevant concentration Estrada, Marcus R. Bzami, Anan Norton, Elizabeth B. White, Jessica A. Vaccine Article Double mutant heat-labile toxin (dmLT) is a novel vaccine adjuvant under development with several different vaccine candidates. Studies using existing dmLT adjuvant stocks require significant dilution to achieve a clinically relevant dose. This dilution leads to wastage of the adjuvant. This manuscript describes a limited formulation study to improve the stability of bulk dmLT at a more clinically relevant concentration (20 µg/mL) with minimal changes to the existing bulk dmLT formulation. In vitro methods were used to evaluate dmLT stability after lyophilization and short-term accelerated stability studies. The addition of the excipient polysorbate 80 (PS80) at 0.05 % to the existing dmLT formulation was identified as the lead modification that provided improved stability of the lyophilized dmLT at 20 µg/mL through 4 weeks at 40 °C. Elsevier Science 2023-02-10 /pmc/articles/PMC9932622/ /pubmed/36658044 http://dx.doi.org/10.1016/j.vaccine.2023.01.005 Text en © 2023 The Author(s) 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 Article
Estrada, Marcus R.
Bzami, Anan
Norton, Elizabeth B.
White, Jessica A.
Identifying a stable bulk dmLT adjuvant formulation at a clinically relevant concentration
title Identifying a stable bulk dmLT adjuvant formulation at a clinically relevant concentration
title_full Identifying a stable bulk dmLT adjuvant formulation at a clinically relevant concentration
title_fullStr Identifying a stable bulk dmLT adjuvant formulation at a clinically relevant concentration
title_full_unstemmed Identifying a stable bulk dmLT adjuvant formulation at a clinically relevant concentration
title_short Identifying a stable bulk dmLT adjuvant formulation at a clinically relevant concentration
title_sort identifying a stable bulk dmlt adjuvant formulation at a clinically relevant concentration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9932622/
https://www.ncbi.nlm.nih.gov/pubmed/36658044
http://dx.doi.org/10.1016/j.vaccine.2023.01.005
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