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A spray freeze dried micropellet based formulation proof-of-concept for a yellow fever vaccine candidate

The stability of live-attenuated viruses is very challenging due to thermal sensitivity; therefore, solid form is usually required (often freeze-dried products). Micropellet technology is a lyophilization technology that has the potential to provide greater flexibility in the presentation of a given...

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Autores principales: Clénet, Didier, Hourquet, Véronique, Woinet, Bertrand, Ponceblanc, Hervé, Vangelisti, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727866/
https://www.ncbi.nlm.nih.gov/pubmed/31306751
http://dx.doi.org/10.1016/j.ejpb.2019.07.008
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author Clénet, Didier
Hourquet, Véronique
Woinet, Bertrand
Ponceblanc, Hervé
Vangelisti, Manuel
author_facet Clénet, Didier
Hourquet, Véronique
Woinet, Bertrand
Ponceblanc, Hervé
Vangelisti, Manuel
author_sort Clénet, Didier
collection PubMed
description The stability of live-attenuated viruses is very challenging due to thermal sensitivity; therefore, solid form is usually required (often freeze-dried products). Micropellet technology is a lyophilization technology that has the potential to provide greater flexibility in the presentation of a given vaccine particularly in multi-dose format or in combination of different vaccines. As a novel vaccine alternative process, this spray freeze-dried (SFD) micropellet technology was evaluated using as a model a yellow fever virus produced in Vero cells (vYF). Screening of excipients was performed in order to optimize physico-chemical properties of the micropellets. Sugar/polymer-based formulations induced high glass transition temperature (Tg), adequate breaking force and attrition resistance of the SFD micropellets. These mechanical parameters and their stability are of considerable importance for the storage, the transport but also the filling process of the SFD micropellets. By adding excipients required to best preserve virus infectivity, an optimal sugar/polymer-based formulation was selected to build micropellets containing vYF. Monodisperse and dried micropellets with a diameter of about 530 µm were obtained, exhibiting similar potency to conventional freeze-dried product in terms of vYF infectious titer when both solid forms were kept under refrigerated conditions (2–8 °C). Comparable kinetics of degradation were observed for vYF formulated in micropellets or as conventional freeze-dried product during an accelerated stability study using incubations at 25 °C and 37 °C over several weeks. The results from this investigation demonstrate the ability to formulate live-attenuated viruses in micropellets. Pharmaceutical applications of this novel vaccine solid form are discussed.
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spelling pubmed-67278662019-09-10 A spray freeze dried micropellet based formulation proof-of-concept for a yellow fever vaccine candidate Clénet, Didier Hourquet, Véronique Woinet, Bertrand Ponceblanc, Hervé Vangelisti, Manuel Eur J Pharm Biopharm Article The stability of live-attenuated viruses is very challenging due to thermal sensitivity; therefore, solid form is usually required (often freeze-dried products). Micropellet technology is a lyophilization technology that has the potential to provide greater flexibility in the presentation of a given vaccine particularly in multi-dose format or in combination of different vaccines. As a novel vaccine alternative process, this spray freeze-dried (SFD) micropellet technology was evaluated using as a model a yellow fever virus produced in Vero cells (vYF). Screening of excipients was performed in order to optimize physico-chemical properties of the micropellets. Sugar/polymer-based formulations induced high glass transition temperature (Tg), adequate breaking force and attrition resistance of the SFD micropellets. These mechanical parameters and their stability are of considerable importance for the storage, the transport but also the filling process of the SFD micropellets. By adding excipients required to best preserve virus infectivity, an optimal sugar/polymer-based formulation was selected to build micropellets containing vYF. Monodisperse and dried micropellets with a diameter of about 530 µm were obtained, exhibiting similar potency to conventional freeze-dried product in terms of vYF infectious titer when both solid forms were kept under refrigerated conditions (2–8 °C). Comparable kinetics of degradation were observed for vYF formulated in micropellets or as conventional freeze-dried product during an accelerated stability study using incubations at 25 °C and 37 °C over several weeks. The results from this investigation demonstrate the ability to formulate live-attenuated viruses in micropellets. Pharmaceutical applications of this novel vaccine solid form are discussed. Elsevier Science 2019-09 /pmc/articles/PMC6727866/ /pubmed/31306751 http://dx.doi.org/10.1016/j.ejpb.2019.07.008 Text en © 2019 The Authors http://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
Clénet, Didier
Hourquet, Véronique
Woinet, Bertrand
Ponceblanc, Hervé
Vangelisti, Manuel
A spray freeze dried micropellet based formulation proof-of-concept for a yellow fever vaccine candidate
title A spray freeze dried micropellet based formulation proof-of-concept for a yellow fever vaccine candidate
title_full A spray freeze dried micropellet based formulation proof-of-concept for a yellow fever vaccine candidate
title_fullStr A spray freeze dried micropellet based formulation proof-of-concept for a yellow fever vaccine candidate
title_full_unstemmed A spray freeze dried micropellet based formulation proof-of-concept for a yellow fever vaccine candidate
title_short A spray freeze dried micropellet based formulation proof-of-concept for a yellow fever vaccine candidate
title_sort spray freeze dried micropellet based formulation proof-of-concept for a yellow fever vaccine candidate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727866/
https://www.ncbi.nlm.nih.gov/pubmed/31306751
http://dx.doi.org/10.1016/j.ejpb.2019.07.008
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