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Challenges and Strategies for a Thorough Characterization of Antibody Acidic Charge Variants
Heterogeneity of therapeutic Monoclonal antibody (mAb) drugs are due to protein variants generated during the manufacturing process. These protein variants can be critical quality attributes (CQAs) depending on their potential impact on drug safety and/or efficacy. To identify CQAs and ensure the dr...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687119/ https://www.ncbi.nlm.nih.gov/pubmed/36354552 http://dx.doi.org/10.3390/bioengineering9110641 |
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author | Liu, Y. Diana Cadang, Lance Bol, Karenna Pan, Xiao Tschudi, Katherine Jazayri, Mansour Camperi, Julien Michels, David Stults, John Harris, Reed J. Yang, Feng |
author_facet | Liu, Y. Diana Cadang, Lance Bol, Karenna Pan, Xiao Tschudi, Katherine Jazayri, Mansour Camperi, Julien Michels, David Stults, John Harris, Reed J. Yang, Feng |
author_sort | Liu, Y. Diana |
collection | PubMed |
description | Heterogeneity of therapeutic Monoclonal antibody (mAb) drugs are due to protein variants generated during the manufacturing process. These protein variants can be critical quality attributes (CQAs) depending on their potential impact on drug safety and/or efficacy. To identify CQAs and ensure the drug product qualities, a thorough characterization is required but challenging due to the complex structure of biotherapeutics. Past characterization studies for basic and acidic variants revealed that full characterizations were limited to the basic charge variants, while the quantitative measurements of acidic variants left gaps. Consequently, the characterization and quantitation of acidic variants are more challenging. A case study of a therapeutic mAb1 accounted for two-thirds of the enriched acidic variants in the initial characterization study. This led to additional investigations, closing the quantification gaps of mAb1 acidic variants. This work demonstrates that a well-designed study with the right choices of analytical methods can play a key role in characterization studies. Thus, the updated strategies for more complete antibody charge variant characterization are recommended. |
format | Online Article Text |
id | pubmed-9687119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96871192022-11-25 Challenges and Strategies for a Thorough Characterization of Antibody Acidic Charge Variants Liu, Y. Diana Cadang, Lance Bol, Karenna Pan, Xiao Tschudi, Katherine Jazayri, Mansour Camperi, Julien Michels, David Stults, John Harris, Reed J. Yang, Feng Bioengineering (Basel) Article Heterogeneity of therapeutic Monoclonal antibody (mAb) drugs are due to protein variants generated during the manufacturing process. These protein variants can be critical quality attributes (CQAs) depending on their potential impact on drug safety and/or efficacy. To identify CQAs and ensure the drug product qualities, a thorough characterization is required but challenging due to the complex structure of biotherapeutics. Past characterization studies for basic and acidic variants revealed that full characterizations were limited to the basic charge variants, while the quantitative measurements of acidic variants left gaps. Consequently, the characterization and quantitation of acidic variants are more challenging. A case study of a therapeutic mAb1 accounted for two-thirds of the enriched acidic variants in the initial characterization study. This led to additional investigations, closing the quantification gaps of mAb1 acidic variants. This work demonstrates that a well-designed study with the right choices of analytical methods can play a key role in characterization studies. Thus, the updated strategies for more complete antibody charge variant characterization are recommended. MDPI 2022-11-03 /pmc/articles/PMC9687119/ /pubmed/36354552 http://dx.doi.org/10.3390/bioengineering9110641 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liu, Y. Diana Cadang, Lance Bol, Karenna Pan, Xiao Tschudi, Katherine Jazayri, Mansour Camperi, Julien Michels, David Stults, John Harris, Reed J. Yang, Feng Challenges and Strategies for a Thorough Characterization of Antibody Acidic Charge Variants |
title | Challenges and Strategies for a Thorough Characterization of Antibody Acidic Charge Variants |
title_full | Challenges and Strategies for a Thorough Characterization of Antibody Acidic Charge Variants |
title_fullStr | Challenges and Strategies for a Thorough Characterization of Antibody Acidic Charge Variants |
title_full_unstemmed | Challenges and Strategies for a Thorough Characterization of Antibody Acidic Charge Variants |
title_short | Challenges and Strategies for a Thorough Characterization of Antibody Acidic Charge Variants |
title_sort | challenges and strategies for a thorough characterization of antibody acidic charge variants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687119/ https://www.ncbi.nlm.nih.gov/pubmed/36354552 http://dx.doi.org/10.3390/bioengineering9110641 |
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