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An Integrated Approach for a Structural and Functional Evaluation of Biosimilars: Implications for Erythropoietin
BACKGROUND: Authorization to market a biosimilar product by the appropriate institutions is expected based on biosimilarity with its originator product. The analogy between the originator and its biosimilar(s) is assessed through safety, purity, and potency analyses. OBJECTIVE: In this study, we pro...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562010/ https://www.ncbi.nlm.nih.gov/pubmed/26334631 http://dx.doi.org/10.1007/s40259-015-0136-3 |
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author | Gianoncelli, Alessandra Bonini, Sara A. Bertuzzi, Michela Guarienti, Michela Vezzoli, Sara Kumar, Rajesh Delbarba, Andrea Mastinu, Andrea Sigala, Sandra Spano, Pierfranco Pani, Luca Pecorelli, Sergio Memo, Maurizio |
author_facet | Gianoncelli, Alessandra Bonini, Sara A. Bertuzzi, Michela Guarienti, Michela Vezzoli, Sara Kumar, Rajesh Delbarba, Andrea Mastinu, Andrea Sigala, Sandra Spano, Pierfranco Pani, Luca Pecorelli, Sergio Memo, Maurizio |
author_sort | Gianoncelli, Alessandra |
collection | PubMed |
description | BACKGROUND: Authorization to market a biosimilar product by the appropriate institutions is expected based on biosimilarity with its originator product. The analogy between the originator and its biosimilar(s) is assessed through safety, purity, and potency analyses. OBJECTIVE: In this study, we proposed a useful quality control system for rapid and economic primary screening of potential biosimilar drugs. For this purpose, chemical and functional characterization of the originator rhEPO alfa and two of its biosimilars was discussed. METHODS: Qualitative and quantitative analyses of the originator rhEPO alfa and its biosimilars were performed using reversed-phase high-performance liquid chromatography (RP-HPLC). The identification of proteins and the separation of isoforms were studied using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF–MS) and two-dimensional gel electrophoresis (2D-PAGE), respectively. Furthermore, the biological activity of these drugs was measured both in vitro, evaluating the TF-1 cell proliferation rate, and in vivo, using the innovative experimental animal model of the zebrafish embryos. RESULTS: Chemical analyses showed that the quantitative concentrations of rhEPO alfa were in agreement with the labeled claims by the corresponding manufacturers. The qualitative analyses performed demonstrated that the three drugs were pure and that they had the same amino acid sequence. Chemical differences were found only at the level of isoforms containing N-glycosylation; however, functional in vitro and in vivo studies did not show any significant differences from a biosimilar point of view. CONCLUSION: These rapid and economic structural and functional analyses were effective in the evaluation of the biosimilarity between the originator rhEPO alfa and the biosimilars analyzed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40259-015-0136-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4562010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-45620102015-09-14 An Integrated Approach for a Structural and Functional Evaluation of Biosimilars: Implications for Erythropoietin Gianoncelli, Alessandra Bonini, Sara A. Bertuzzi, Michela Guarienti, Michela Vezzoli, Sara Kumar, Rajesh Delbarba, Andrea Mastinu, Andrea Sigala, Sandra Spano, Pierfranco Pani, Luca Pecorelli, Sergio Memo, Maurizio BioDrugs Original Research Article BACKGROUND: Authorization to market a biosimilar product by the appropriate institutions is expected based on biosimilarity with its originator product. The analogy between the originator and its biosimilar(s) is assessed through safety, purity, and potency analyses. OBJECTIVE: In this study, we proposed a useful quality control system for rapid and economic primary screening of potential biosimilar drugs. For this purpose, chemical and functional characterization of the originator rhEPO alfa and two of its biosimilars was discussed. METHODS: Qualitative and quantitative analyses of the originator rhEPO alfa and its biosimilars were performed using reversed-phase high-performance liquid chromatography (RP-HPLC). The identification of proteins and the separation of isoforms were studied using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF–MS) and two-dimensional gel electrophoresis (2D-PAGE), respectively. Furthermore, the biological activity of these drugs was measured both in vitro, evaluating the TF-1 cell proliferation rate, and in vivo, using the innovative experimental animal model of the zebrafish embryos. RESULTS: Chemical analyses showed that the quantitative concentrations of rhEPO alfa were in agreement with the labeled claims by the corresponding manufacturers. The qualitative analyses performed demonstrated that the three drugs were pure and that they had the same amino acid sequence. Chemical differences were found only at the level of isoforms containing N-glycosylation; however, functional in vitro and in vivo studies did not show any significant differences from a biosimilar point of view. CONCLUSION: These rapid and economic structural and functional analyses were effective in the evaluation of the biosimilarity between the originator rhEPO alfa and the biosimilars analyzed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40259-015-0136-3) contains supplementary material, which is available to authorized users. Springer International Publishing 2015-09-03 2015 /pmc/articles/PMC4562010/ /pubmed/26334631 http://dx.doi.org/10.1007/s40259-015-0136-3 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial 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. |
spellingShingle | Original Research Article Gianoncelli, Alessandra Bonini, Sara A. Bertuzzi, Michela Guarienti, Michela Vezzoli, Sara Kumar, Rajesh Delbarba, Andrea Mastinu, Andrea Sigala, Sandra Spano, Pierfranco Pani, Luca Pecorelli, Sergio Memo, Maurizio An Integrated Approach for a Structural and Functional Evaluation of Biosimilars: Implications for Erythropoietin |
title | An Integrated Approach for a Structural and Functional Evaluation of Biosimilars: Implications for Erythropoietin |
title_full | An Integrated Approach for a Structural and Functional Evaluation of Biosimilars: Implications for Erythropoietin |
title_fullStr | An Integrated Approach for a Structural and Functional Evaluation of Biosimilars: Implications for Erythropoietin |
title_full_unstemmed | An Integrated Approach for a Structural and Functional Evaluation of Biosimilars: Implications for Erythropoietin |
title_short | An Integrated Approach for a Structural and Functional Evaluation of Biosimilars: Implications for Erythropoietin |
title_sort | integrated approach for a structural and functional evaluation of biosimilars: implications for erythropoietin |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562010/ https://www.ncbi.nlm.nih.gov/pubmed/26334631 http://dx.doi.org/10.1007/s40259-015-0136-3 |
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