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Purification of influenza virus‐like particles using sulfated cellulose membrane adsorbers
BACKGROUND: Vaccines based on virus‐like particles (VLPs) are an alternative to inactivated viral vaccines that combine good safety profiles with strong immunogenicity. In order to be economically competitive, efficient manufacturing is required, in particular downstream processing, which often acco...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033026/ https://www.ncbi.nlm.nih.gov/pubmed/30008506 http://dx.doi.org/10.1002/jctb.5474 |
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author | B Carvalho, Sofia Fortuna, A Raquel Wolff, Michael W Peixoto, Cristina M Alves, Paula Reichl, Udo JT Carrondo, Manuel |
author_facet | B Carvalho, Sofia Fortuna, A Raquel Wolff, Michael W Peixoto, Cristina M Alves, Paula Reichl, Udo JT Carrondo, Manuel |
author_sort | B Carvalho, Sofia |
collection | PubMed |
description | BACKGROUND: Vaccines based on virus‐like particles (VLPs) are an alternative to inactivated viral vaccines that combine good safety profiles with strong immunogenicity. In order to be economically competitive, efficient manufacturing is required, in particular downstream processing, which often accounts for major production costs. This study describes the optimization and establishment of a chromatography capturing technique using sulfated cellulose membrane adsorbers (SCMA) for purification of influenza VLPs. RESULTS: Using a design of experiments approach, the critical factors for SCMA performance were described and optimized. For optimal conditions (membrane ligand density: 15.4 µmol cm(−2), salt concentration of the loading buffer: 24 mmol L(‐1) NaCl, and elution buffer: 920 mmol L(‐1) NaCl, as well as the corresponding flow rates: 0.24 and 1.4 mL min(−1)), a yield of 80% in the product fraction was obtained. No loss of VLPs was detected in the flowthrough fraction. Removal of total protein and DNA impurities were higher than 89% and 80%, respectively. CONCLUSION: Use of SCMA represents a significant improvement compared with conventional ion exchanger membrane adsorbers. As the method proposed is easily scalable and reduces the number of steps required compared with conventional purification methods, SCMA could qualify as a generic platform for purification of VLP‐based influenza vaccines. © 2017 The Authors. Journal of Chemical Technology & Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. |
format | Online Article Text |
id | pubmed-6033026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60330262018-07-12 Purification of influenza virus‐like particles using sulfated cellulose membrane adsorbers B Carvalho, Sofia Fortuna, A Raquel Wolff, Michael W Peixoto, Cristina M Alves, Paula Reichl, Udo JT Carrondo, Manuel J Chem Technol Biotechnol Research Articles BACKGROUND: Vaccines based on virus‐like particles (VLPs) are an alternative to inactivated viral vaccines that combine good safety profiles with strong immunogenicity. In order to be economically competitive, efficient manufacturing is required, in particular downstream processing, which often accounts for major production costs. This study describes the optimization and establishment of a chromatography capturing technique using sulfated cellulose membrane adsorbers (SCMA) for purification of influenza VLPs. RESULTS: Using a design of experiments approach, the critical factors for SCMA performance were described and optimized. For optimal conditions (membrane ligand density: 15.4 µmol cm(−2), salt concentration of the loading buffer: 24 mmol L(‐1) NaCl, and elution buffer: 920 mmol L(‐1) NaCl, as well as the corresponding flow rates: 0.24 and 1.4 mL min(−1)), a yield of 80% in the product fraction was obtained. No loss of VLPs was detected in the flowthrough fraction. Removal of total protein and DNA impurities were higher than 89% and 80%, respectively. CONCLUSION: Use of SCMA represents a significant improvement compared with conventional ion exchanger membrane adsorbers. As the method proposed is easily scalable and reduces the number of steps required compared with conventional purification methods, SCMA could qualify as a generic platform for purification of VLP‐based influenza vaccines. © 2017 The Authors. Journal of Chemical Technology & Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. John Wiley & Sons, Ltd 2017-12-16 2018-07 /pmc/articles/PMC6033026/ /pubmed/30008506 http://dx.doi.org/10.1002/jctb.5474 Text en © 2017 The Authors. Journal of Chemical Technology & Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles B Carvalho, Sofia Fortuna, A Raquel Wolff, Michael W Peixoto, Cristina M Alves, Paula Reichl, Udo JT Carrondo, Manuel Purification of influenza virus‐like particles using sulfated cellulose membrane adsorbers |
title | Purification of influenza virus‐like particles using sulfated cellulose membrane adsorbers |
title_full | Purification of influenza virus‐like particles using sulfated cellulose membrane adsorbers |
title_fullStr | Purification of influenza virus‐like particles using sulfated cellulose membrane adsorbers |
title_full_unstemmed | Purification of influenza virus‐like particles using sulfated cellulose membrane adsorbers |
title_short | Purification of influenza virus‐like particles using sulfated cellulose membrane adsorbers |
title_sort | purification of influenza virus‐like particles using sulfated cellulose membrane adsorbers |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033026/ https://www.ncbi.nlm.nih.gov/pubmed/30008506 http://dx.doi.org/10.1002/jctb.5474 |
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