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Development of a solid dosage platform for the oral delivery of bilayer vesicles

Within this work, we develop vesicles incorporating sub-unit antigens as solid dosage forms suitable for the oral delivery of vaccines. Using a combination of trehalose, dextran and mannitol, freeze-dried oral disintegrating tablets were formed which upon rehydration release bilayer vesicles incorpo...

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Detalles Bibliográficos
Autores principales: Wilkhu, Jitinder S., McNeil, Sarah E., Anderson, David E., Kirchmeier, Marc, Perrie, Yvonne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science B.V 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611758/
https://www.ncbi.nlm.nih.gov/pubmed/28619620
http://dx.doi.org/10.1016/j.ejps.2017.06.014
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author Wilkhu, Jitinder S.
McNeil, Sarah E.
Anderson, David E.
Kirchmeier, Marc
Perrie, Yvonne
author_facet Wilkhu, Jitinder S.
McNeil, Sarah E.
Anderson, David E.
Kirchmeier, Marc
Perrie, Yvonne
author_sort Wilkhu, Jitinder S.
collection PubMed
description Within this work, we develop vesicles incorporating sub-unit antigens as solid dosage forms suitable for the oral delivery of vaccines. Using a combination of trehalose, dextran and mannitol, freeze-dried oral disintegrating tablets were formed which upon rehydration release bilayer vesicles incorporating antigen. Initial studies focused on the optimisation of the freeze-dry cycle and subsequently excipient content was optimised by testing tablet hardness, disintegration time and moisture content. The use of 10% mannitol and 10% dextran produced durable tablets which offered strong resistance to mechanical damage yet appropriate disintegration times and dispersed to release niosomes-entrapping antigen. From these studies, we have formulated a bilayer vesicle vaccine delivery system as rapid disintegrating tablets and capsules.
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spelling pubmed-56117582017-10-15 Development of a solid dosage platform for the oral delivery of bilayer vesicles Wilkhu, Jitinder S. McNeil, Sarah E. Anderson, David E. Kirchmeier, Marc Perrie, Yvonne Eur J Pharm Sci Article Within this work, we develop vesicles incorporating sub-unit antigens as solid dosage forms suitable for the oral delivery of vaccines. Using a combination of trehalose, dextran and mannitol, freeze-dried oral disintegrating tablets were formed which upon rehydration release bilayer vesicles incorporating antigen. Initial studies focused on the optimisation of the freeze-dry cycle and subsequently excipient content was optimised by testing tablet hardness, disintegration time and moisture content. The use of 10% mannitol and 10% dextran produced durable tablets which offered strong resistance to mechanical damage yet appropriate disintegration times and dispersed to release niosomes-entrapping antigen. From these studies, we have formulated a bilayer vesicle vaccine delivery system as rapid disintegrating tablets and capsules. Elsevier Science B.V 2017-10-15 /pmc/articles/PMC5611758/ /pubmed/28619620 http://dx.doi.org/10.1016/j.ejps.2017.06.014 Text en © 2017 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
Wilkhu, Jitinder S.
McNeil, Sarah E.
Anderson, David E.
Kirchmeier, Marc
Perrie, Yvonne
Development of a solid dosage platform for the oral delivery of bilayer vesicles
title Development of a solid dosage platform for the oral delivery of bilayer vesicles
title_full Development of a solid dosage platform for the oral delivery of bilayer vesicles
title_fullStr Development of a solid dosage platform for the oral delivery of bilayer vesicles
title_full_unstemmed Development of a solid dosage platform for the oral delivery of bilayer vesicles
title_short Development of a solid dosage platform for the oral delivery of bilayer vesicles
title_sort development of a solid dosage platform for the oral delivery of bilayer vesicles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611758/
https://www.ncbi.nlm.nih.gov/pubmed/28619620
http://dx.doi.org/10.1016/j.ejps.2017.06.014
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