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Current Analytical Strategies for Antibody–Drug Conjugates in Biomatrices
Antibody–drug conjugates (ADCs) are a new class of biotherapeutics, consisting of a cytotoxic payload covalently bound to an antibody by a linker. Ligand-binding assay (LBA) and liquid chromatography-mass spectrometry (LC-MS) are the favored techniques for the analysis of ADCs in biomatrices. The go...
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/PMC9572530/ https://www.ncbi.nlm.nih.gov/pubmed/36234836 http://dx.doi.org/10.3390/molecules27196299 |
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author | Qin, Qiuping Gong, Likun |
author_facet | Qin, Qiuping Gong, Likun |
author_sort | Qin, Qiuping |
collection | PubMed |
description | Antibody–drug conjugates (ADCs) are a new class of biotherapeutics, consisting of a cytotoxic payload covalently bound to an antibody by a linker. Ligand-binding assay (LBA) and liquid chromatography-mass spectrometry (LC-MS) are the favored techniques for the analysis of ADCs in biomatrices. The goal of our review is to provide current strategies related to a series of bioanalytical assays for pharmacokinetics (PK) and anti-drug antibody (ADA) assessments. Furthermore, the strengths and limitations of LBA and LC-MS platforms are compared. Finally, potential factors that affect the performance of the developed assays are also provided. It is hoped that the review can provide valuable insights to bioanalytical scientists on the use of an integrated analytical strategy involving LBA and LC–MS for the bioanalysis of ADCs and related immunogenicity evaluation. |
format | Online Article Text |
id | pubmed-9572530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95725302022-10-17 Current Analytical Strategies for Antibody–Drug Conjugates in Biomatrices Qin, Qiuping Gong, Likun Molecules Review Antibody–drug conjugates (ADCs) are a new class of biotherapeutics, consisting of a cytotoxic payload covalently bound to an antibody by a linker. Ligand-binding assay (LBA) and liquid chromatography-mass spectrometry (LC-MS) are the favored techniques for the analysis of ADCs in biomatrices. The goal of our review is to provide current strategies related to a series of bioanalytical assays for pharmacokinetics (PK) and anti-drug antibody (ADA) assessments. Furthermore, the strengths and limitations of LBA and LC-MS platforms are compared. Finally, potential factors that affect the performance of the developed assays are also provided. It is hoped that the review can provide valuable insights to bioanalytical scientists on the use of an integrated analytical strategy involving LBA and LC–MS for the bioanalysis of ADCs and related immunogenicity evaluation. MDPI 2022-09-24 /pmc/articles/PMC9572530/ /pubmed/36234836 http://dx.doi.org/10.3390/molecules27196299 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 | Review Qin, Qiuping Gong, Likun Current Analytical Strategies for Antibody–Drug Conjugates in Biomatrices |
title | Current Analytical Strategies for Antibody–Drug Conjugates in Biomatrices |
title_full | Current Analytical Strategies for Antibody–Drug Conjugates in Biomatrices |
title_fullStr | Current Analytical Strategies for Antibody–Drug Conjugates in Biomatrices |
title_full_unstemmed | Current Analytical Strategies for Antibody–Drug Conjugates in Biomatrices |
title_short | Current Analytical Strategies for Antibody–Drug Conjugates in Biomatrices |
title_sort | current analytical strategies for antibody–drug conjugates in biomatrices |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9572530/ https://www.ncbi.nlm.nih.gov/pubmed/36234836 http://dx.doi.org/10.3390/molecules27196299 |
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