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Control of Protein Particle Formation During Ultrafiltration/Diafiltration Through Interfacial Protection
This study investigates the mechanism of protein particle formation during ultrafiltration/diafiltration (UF/DF), finding that agitation drives particle formation by promoting protein-interface adsorption and desorption. Low conductivity and the presence of surfactant reduced the level of particle f...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4284022/ https://www.ncbi.nlm.nih.gov/pubmed/24449131 http://dx.doi.org/10.1002/jps.23861 |
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author | Callahan, Daniel J Stanley, Bradford Li, Yuling |
author_facet | Callahan, Daniel J Stanley, Bradford Li, Yuling |
author_sort | Callahan, Daniel J |
collection | PubMed |
description | This study investigates the mechanism of protein particle formation during ultrafiltration/diafiltration (UF/DF), finding that agitation drives particle formation by promoting protein-interface adsorption and desorption. Low conductivity and the presence of surfactant reduced the level of particle formation in small-scale stirring studies, and the same trends were observed in pumping and UF/DF. Polysorbate 80 (PS80) and hydroxypropyl-β-cyclodextrin (HPβCD) reduced particle formation in UF/DF by factors of 15 and 4, respectively. Measurements of conformational stability, colloidal stability, and surface tension demonstrated that PS80 protects against particle formation by preventing protein-interface adsorption, low conductivity improves the colloidal stability of the protein, and the mechanism of action of HPβCD remains unclear. This work demonstrates that interfacial adsorption–desorption of the protein during UF/DF is the principal cause of particle formation, that the level of surfactant-free particle formation depends on the colloidal stability of the protein, and that the inclusion of surfactant greatly reduces in-process particle formation during UF/DF. |
format | Online Article Text |
id | pubmed-4284022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42840222015-01-14 Control of Protein Particle Formation During Ultrafiltration/Diafiltration Through Interfacial Protection Callahan, Daniel J Stanley, Bradford Li, Yuling J Pharm Sci Pharmaceutical Biotechnology This study investigates the mechanism of protein particle formation during ultrafiltration/diafiltration (UF/DF), finding that agitation drives particle formation by promoting protein-interface adsorption and desorption. Low conductivity and the presence of surfactant reduced the level of particle formation in small-scale stirring studies, and the same trends were observed in pumping and UF/DF. Polysorbate 80 (PS80) and hydroxypropyl-β-cyclodextrin (HPβCD) reduced particle formation in UF/DF by factors of 15 and 4, respectively. Measurements of conformational stability, colloidal stability, and surface tension demonstrated that PS80 protects against particle formation by preventing protein-interface adsorption, low conductivity improves the colloidal stability of the protein, and the mechanism of action of HPβCD remains unclear. This work demonstrates that interfacial adsorption–desorption of the protein during UF/DF is the principal cause of particle formation, that the level of surfactant-free particle formation depends on the colloidal stability of the protein, and that the inclusion of surfactant greatly reduces in-process particle formation during UF/DF. BlackWell Publishing Ltd 2014-03 2014-01-21 /pmc/articles/PMC4284022/ /pubmed/24449131 http://dx.doi.org/10.1002/jps.23861 Text en © 2014 The Authors. Journal of Pharmaceutical Sciences published by Wiley Periodicals, Inc. and the American Pharmacists Association http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Pharmaceutical Biotechnology Callahan, Daniel J Stanley, Bradford Li, Yuling Control of Protein Particle Formation During Ultrafiltration/Diafiltration Through Interfacial Protection |
title | Control of Protein Particle Formation During Ultrafiltration/Diafiltration Through Interfacial Protection |
title_full | Control of Protein Particle Formation During Ultrafiltration/Diafiltration Through Interfacial Protection |
title_fullStr | Control of Protein Particle Formation During Ultrafiltration/Diafiltration Through Interfacial Protection |
title_full_unstemmed | Control of Protein Particle Formation During Ultrafiltration/Diafiltration Through Interfacial Protection |
title_short | Control of Protein Particle Formation During Ultrafiltration/Diafiltration Through Interfacial Protection |
title_sort | control of protein particle formation during ultrafiltration/diafiltration through interfacial protection |
topic | Pharmaceutical Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4284022/ https://www.ncbi.nlm.nih.gov/pubmed/24449131 http://dx.doi.org/10.1002/jps.23861 |
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