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Characterization of Particles in Protein Solutions: Reaching the Limits of Current Technologies
Recent publications have emphasized the lack of characterization methods available for protein particles in a size range comprised between 0.1 and 10 μm and the potential risk of immunogenicity associated with such particles. In the present paper, we have investigated the performance of light obscur...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer US
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977008/ https://www.ncbi.nlm.nih.gov/pubmed/20953747 http://dx.doi.org/10.1208/s12248-010-9233-x |
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author | Demeule, Barthélemy Messick, Steven Shire, Steven J. Liu, Jun |
author_facet | Demeule, Barthélemy Messick, Steven Shire, Steven J. Liu, Jun |
author_sort | Demeule, Barthélemy |
collection | PubMed |
description | Recent publications have emphasized the lack of characterization methods available for protein particles in a size range comprised between 0.1 and 10 μm and the potential risk of immunogenicity associated with such particles. In the present paper, we have investigated the performance of light obscuration, flow microscopy, and Coulter counter instruments for particle counting and sizing in protein formulations. We focused on particles 2–10 μm in diameter and studied the effect of silicon oil droplets originating from the barrel of pre-filled syringes, as well as the effect of high protein concentrations (up to 150 mg/ml) on the accuracy of particle characterization. Silicon oil was demonstrated to contribute significantly to the particle counts observed in pre-filled syringes. Inconsistent results were observed between different protein concentrations in the range 7.5–150 mg/ml for particles <10 μm studied by optical techniques (light obscuration and flow microscopy). However, the Coulter counter measurements were consistent across the same studied concentration range but required sufficient solution conductivity from the formulation buffer or excipients. Our results show that currently available technologies, while allowing comparisons between samples of a given protein at a fixed concentration, may be unable to measure particle numbers accurately in a variety of protein formulations, e.g., at high concentration in sugar-based formulations. |
format | Text |
id | pubmed-2977008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-29770082010-12-15 Characterization of Particles in Protein Solutions: Reaching the Limits of Current Technologies Demeule, Barthélemy Messick, Steven Shire, Steven J. Liu, Jun AAPS J Research Article Recent publications have emphasized the lack of characterization methods available for protein particles in a size range comprised between 0.1 and 10 μm and the potential risk of immunogenicity associated with such particles. In the present paper, we have investigated the performance of light obscuration, flow microscopy, and Coulter counter instruments for particle counting and sizing in protein formulations. We focused on particles 2–10 μm in diameter and studied the effect of silicon oil droplets originating from the barrel of pre-filled syringes, as well as the effect of high protein concentrations (up to 150 mg/ml) on the accuracy of particle characterization. Silicon oil was demonstrated to contribute significantly to the particle counts observed in pre-filled syringes. Inconsistent results were observed between different protein concentrations in the range 7.5–150 mg/ml for particles <10 μm studied by optical techniques (light obscuration and flow microscopy). However, the Coulter counter measurements were consistent across the same studied concentration range but required sufficient solution conductivity from the formulation buffer or excipients. Our results show that currently available technologies, while allowing comparisons between samples of a given protein at a fixed concentration, may be unable to measure particle numbers accurately in a variety of protein formulations, e.g., at high concentration in sugar-based formulations. Springer US 2010-10-16 /pmc/articles/PMC2977008/ /pubmed/20953747 http://dx.doi.org/10.1208/s12248-010-9233-x Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Research Article Demeule, Barthélemy Messick, Steven Shire, Steven J. Liu, Jun Characterization of Particles in Protein Solutions: Reaching the Limits of Current Technologies |
title | Characterization of Particles in Protein Solutions: Reaching the Limits of Current Technologies |
title_full | Characterization of Particles in Protein Solutions: Reaching the Limits of Current Technologies |
title_fullStr | Characterization of Particles in Protein Solutions: Reaching the Limits of Current Technologies |
title_full_unstemmed | Characterization of Particles in Protein Solutions: Reaching the Limits of Current Technologies |
title_short | Characterization of Particles in Protein Solutions: Reaching the Limits of Current Technologies |
title_sort | characterization of particles in protein solutions: reaching the limits of current technologies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977008/ https://www.ncbi.nlm.nih.gov/pubmed/20953747 http://dx.doi.org/10.1208/s12248-010-9233-x |
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