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Determination of immunogenic proteins in biopharmaceuticals by UHPLC–MS amino acid analysis

Nowadays, there is a growing interest in innovative and more efficient therapeutics—biopharmaceuticals, based on peptides or proteins. There are increased demands on quality control of such therapeutics. One of the methods usually used for characterization and quantification of biopharmaceuticals is...

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Autores principales: Piestansky, Juraj, Galba, Jaroslav, Olesova, Dominika, Kovacech, Branislav, Kovac, Andrej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661756/
https://www.ncbi.nlm.nih.gov/pubmed/31384811
http://dx.doi.org/10.1186/s13065-019-0581-z
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author Piestansky, Juraj
Galba, Jaroslav
Olesova, Dominika
Kovacech, Branislav
Kovac, Andrej
author_facet Piestansky, Juraj
Galba, Jaroslav
Olesova, Dominika
Kovacech, Branislav
Kovac, Andrej
author_sort Piestansky, Juraj
collection PubMed
description Nowadays, there is a growing interest in innovative and more efficient therapeutics—biopharmaceuticals, based on peptides or proteins. There are increased demands on quality control of such therapeutics. One of the methods usually used for characterization and quantification of biopharmaceuticals is amino acid analysis. In this work, a modern advanced analytical method based on precolumn derivatization and reversed-phase ultra high-performance liquid chromatography in combination with single quadrupole mass spectrometer was developed for amino acid analysis in different protein samples—model sample of bovine serum albumin, sample of strong immunogenic protein keyhole limpet hemocyanin, and sample of drug etanercept present in commercially available biopharmaceutical Enbrel. The method used isotopically labeled internal standards and was validated according to the International Council for Harmonisation guideline. The developed method was characterized by favorable performance and validation parameters, such as time of analysis (6 min), specificity, linearity (r(2) ≥ 0.99), limit of detection (0.009–0.822 µM), limit of quantification (1–2.5 µM), accuracy (recovery in the range 90–102.8%), intra-day (RSD in the range 0.25–11.97%) and inter-day precision (RSD in the range 1.67–11.57%), or stability (RE ≤ 12%). According to these findings, the developed amino acid analysis approach is suitable for routine use in areas of peptide/protein quantification, such as quality control laboratories of biopharmaceutical companies. [Image: see text]
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spelling pubmed-66617562019-08-05 Determination of immunogenic proteins in biopharmaceuticals by UHPLC–MS amino acid analysis Piestansky, Juraj Galba, Jaroslav Olesova, Dominika Kovacech, Branislav Kovac, Andrej BMC Chem Research Article Nowadays, there is a growing interest in innovative and more efficient therapeutics—biopharmaceuticals, based on peptides or proteins. There are increased demands on quality control of such therapeutics. One of the methods usually used for characterization and quantification of biopharmaceuticals is amino acid analysis. In this work, a modern advanced analytical method based on precolumn derivatization and reversed-phase ultra high-performance liquid chromatography in combination with single quadrupole mass spectrometer was developed for amino acid analysis in different protein samples—model sample of bovine serum albumin, sample of strong immunogenic protein keyhole limpet hemocyanin, and sample of drug etanercept present in commercially available biopharmaceutical Enbrel. The method used isotopically labeled internal standards and was validated according to the International Council for Harmonisation guideline. The developed method was characterized by favorable performance and validation parameters, such as time of analysis (6 min), specificity, linearity (r(2) ≥ 0.99), limit of detection (0.009–0.822 µM), limit of quantification (1–2.5 µM), accuracy (recovery in the range 90–102.8%), intra-day (RSD in the range 0.25–11.97%) and inter-day precision (RSD in the range 1.67–11.57%), or stability (RE ≤ 12%). According to these findings, the developed amino acid analysis approach is suitable for routine use in areas of peptide/protein quantification, such as quality control laboratories of biopharmaceutical companies. [Image: see text] Springer International Publishing 2019-05-10 /pmc/articles/PMC6661756/ /pubmed/31384811 http://dx.doi.org/10.1186/s13065-019-0581-z Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Piestansky, Juraj
Galba, Jaroslav
Olesova, Dominika
Kovacech, Branislav
Kovac, Andrej
Determination of immunogenic proteins in biopharmaceuticals by UHPLC–MS amino acid analysis
title Determination of immunogenic proteins in biopharmaceuticals by UHPLC–MS amino acid analysis
title_full Determination of immunogenic proteins in biopharmaceuticals by UHPLC–MS amino acid analysis
title_fullStr Determination of immunogenic proteins in biopharmaceuticals by UHPLC–MS amino acid analysis
title_full_unstemmed Determination of immunogenic proteins in biopharmaceuticals by UHPLC–MS amino acid analysis
title_short Determination of immunogenic proteins in biopharmaceuticals by UHPLC–MS amino acid analysis
title_sort determination of immunogenic proteins in biopharmaceuticals by uhplc–ms amino acid analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661756/
https://www.ncbi.nlm.nih.gov/pubmed/31384811
http://dx.doi.org/10.1186/s13065-019-0581-z
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