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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...

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Detalles Bibliográficos
Autores principales: Callahan, Daniel J, Stanley, Bradford, Li, Yuling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
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.
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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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