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In depth characterization of physicochemical critical quality attributes of a clinical drug-dendrimer conjugate

A deep and detailed understanding of drug-dendrimer conjugates key properties is needed to define the critical quality attributes that affect drug product performance. The characterization must be executed both in the formulation media and in biological matrices. This, nevertheless, is challenging o...

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Autores principales: Sonzini, Silvia, Caputo, Fanny, Mehn, Dora, Calzolai, Luigi, Even Borgos, Sven, Hyldbakk, Astrid, Treacher, Kevin, Li, Weimin, Jackman, Mark, Mahmoudi, Najet, Jayne Lawrence, M., Patterson, Claire, Owen, David, Ashford, Marianne, Akhtar, Nadim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier/North-Holland Biomedical Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157317/
https://www.ncbi.nlm.nih.gov/pubmed/37003312
http://dx.doi.org/10.1016/j.ijpharm.2023.122905
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author Sonzini, Silvia
Caputo, Fanny
Mehn, Dora
Calzolai, Luigi
Even Borgos, Sven
Hyldbakk, Astrid
Treacher, Kevin
Li, Weimin
Jackman, Mark
Mahmoudi, Najet
Jayne Lawrence, M.
Patterson, Claire
Owen, David
Ashford, Marianne
Akhtar, Nadim
author_facet Sonzini, Silvia
Caputo, Fanny
Mehn, Dora
Calzolai, Luigi
Even Borgos, Sven
Hyldbakk, Astrid
Treacher, Kevin
Li, Weimin
Jackman, Mark
Mahmoudi, Najet
Jayne Lawrence, M.
Patterson, Claire
Owen, David
Ashford, Marianne
Akhtar, Nadim
author_sort Sonzini, Silvia
collection PubMed
description A deep and detailed understanding of drug-dendrimer conjugates key properties is needed to define the critical quality attributes that affect drug product performance. The characterization must be executed both in the formulation media and in biological matrices. This, nevertheless, is challenging on account of a very limited number of suitable, established methods for characterizing the physicochemical properties, stability, and interaction with biological environment of complex drug-dendrimer conjugates. In order to fully characterize AZD0466, a drug-dendrimer conjugate currently under clinical development by AstraZeneca, a collaboration was initiated with the European Nanomedicine Characterisation Laboratory to deploy a state-of-the-art multi-step approach to measure physicochemical properties. An incremental complexity characterization approach was applied to two batches of AZD0466 and the corresponding dendrimer not carrying any drug, SPL-8984. Thus, the aim of this work is to guide in depth characterization efforts in the analysis of drug-dendrimer conjugates. Additionally, it serves to highlight the importance of using the adequate complementary techniques to measure physical and chemical stability in both simple and biological media, to drive a complex drug-dendrimer conjugate product from discovery to clinical development.
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spelling pubmed-101573172023-05-05 In depth characterization of physicochemical critical quality attributes of a clinical drug-dendrimer conjugate Sonzini, Silvia Caputo, Fanny Mehn, Dora Calzolai, Luigi Even Borgos, Sven Hyldbakk, Astrid Treacher, Kevin Li, Weimin Jackman, Mark Mahmoudi, Najet Jayne Lawrence, M. Patterson, Claire Owen, David Ashford, Marianne Akhtar, Nadim Int J Pharm Article A deep and detailed understanding of drug-dendrimer conjugates key properties is needed to define the critical quality attributes that affect drug product performance. The characterization must be executed both in the formulation media and in biological matrices. This, nevertheless, is challenging on account of a very limited number of suitable, established methods for characterizing the physicochemical properties, stability, and interaction with biological environment of complex drug-dendrimer conjugates. In order to fully characterize AZD0466, a drug-dendrimer conjugate currently under clinical development by AstraZeneca, a collaboration was initiated with the European Nanomedicine Characterisation Laboratory to deploy a state-of-the-art multi-step approach to measure physicochemical properties. An incremental complexity characterization approach was applied to two batches of AZD0466 and the corresponding dendrimer not carrying any drug, SPL-8984. Thus, the aim of this work is to guide in depth characterization efforts in the analysis of drug-dendrimer conjugates. Additionally, it serves to highlight the importance of using the adequate complementary techniques to measure physical and chemical stability in both simple and biological media, to drive a complex drug-dendrimer conjugate product from discovery to clinical development. Elsevier/North-Holland Biomedical Press 2023-04-25 /pmc/articles/PMC10157317/ /pubmed/37003312 http://dx.doi.org/10.1016/j.ijpharm.2023.122905 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Sonzini, Silvia
Caputo, Fanny
Mehn, Dora
Calzolai, Luigi
Even Borgos, Sven
Hyldbakk, Astrid
Treacher, Kevin
Li, Weimin
Jackman, Mark
Mahmoudi, Najet
Jayne Lawrence, M.
Patterson, Claire
Owen, David
Ashford, Marianne
Akhtar, Nadim
In depth characterization of physicochemical critical quality attributes of a clinical drug-dendrimer conjugate
title In depth characterization of physicochemical critical quality attributes of a clinical drug-dendrimer conjugate
title_full In depth characterization of physicochemical critical quality attributes of a clinical drug-dendrimer conjugate
title_fullStr In depth characterization of physicochemical critical quality attributes of a clinical drug-dendrimer conjugate
title_full_unstemmed In depth characterization of physicochemical critical quality attributes of a clinical drug-dendrimer conjugate
title_short In depth characterization of physicochemical critical quality attributes of a clinical drug-dendrimer conjugate
title_sort in depth characterization of physicochemical critical quality attributes of a clinical drug-dendrimer conjugate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157317/
https://www.ncbi.nlm.nih.gov/pubmed/37003312
http://dx.doi.org/10.1016/j.ijpharm.2023.122905
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