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Human Serum Albumin in the Presence of AGuIX Nanoagents: Structure Stabilisation without Direct Interaction

The gadolinium-based nanoagent named AGuIX(®) is a unique radiosensitizer and contrast agent which improves the performance of radiotherapy and medical imaging. Currently tested in clinical trials, AGuIX(®) is administrated to patients via intravenous injection. The presence of nanoparticles in the...

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Autores principales: Yang, Xiaomin, Bolsa-Ferruz, Marta, Marichal, Laurent, Porcel, Erika, Salado-Leza, Daniela, Lux, François, Tillement, Olivier, Renault, Jean-Philippe, Pin, Serge, Wien, Frank, Lacombe, Sandrine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7369717/
https://www.ncbi.nlm.nih.gov/pubmed/32630060
http://dx.doi.org/10.3390/ijms21134673
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author Yang, Xiaomin
Bolsa-Ferruz, Marta
Marichal, Laurent
Porcel, Erika
Salado-Leza, Daniela
Lux, François
Tillement, Olivier
Renault, Jean-Philippe
Pin, Serge
Wien, Frank
Lacombe, Sandrine
author_facet Yang, Xiaomin
Bolsa-Ferruz, Marta
Marichal, Laurent
Porcel, Erika
Salado-Leza, Daniela
Lux, François
Tillement, Olivier
Renault, Jean-Philippe
Pin, Serge
Wien, Frank
Lacombe, Sandrine
author_sort Yang, Xiaomin
collection PubMed
description The gadolinium-based nanoagent named AGuIX(®) is a unique radiosensitizer and contrast agent which improves the performance of radiotherapy and medical imaging. Currently tested in clinical trials, AGuIX(®) is administrated to patients via intravenous injection. The presence of nanoparticles in the blood stream may induce harmful effects due to undesired interactions with blood components. Thus, there is an emerging need to understand the impact of these nanoagents when meeting blood proteins. In this work, the influence of nanoagents on the structure and stability of the most abundant blood protein, human serum albumin, is presented. Synchrotron radiation circular dichroism showed that AGuIX(®) does not bind to the protein, even at the high ratio of 45 nanoparticles per protein at 3 mg/L. However, it increases the stability of the albumin. Isothermal thermodynamic calorimetry and fluorescence emission spectroscopy demonstrated that the effect is due to preferential hydration processes. Thus, this study confirms that intravenous injection of AGuIX(®) presents limited risks of perturbing the blood stream. In a wider view, the methodology developed in this work may be applied to rapidly evaluate the impact and risk of other nano-products that could come into contact with the bloodstream.
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spelling pubmed-73697172020-07-21 Human Serum Albumin in the Presence of AGuIX Nanoagents: Structure Stabilisation without Direct Interaction Yang, Xiaomin Bolsa-Ferruz, Marta Marichal, Laurent Porcel, Erika Salado-Leza, Daniela Lux, François Tillement, Olivier Renault, Jean-Philippe Pin, Serge Wien, Frank Lacombe, Sandrine Int J Mol Sci Article The gadolinium-based nanoagent named AGuIX(®) is a unique radiosensitizer and contrast agent which improves the performance of radiotherapy and medical imaging. Currently tested in clinical trials, AGuIX(®) is administrated to patients via intravenous injection. The presence of nanoparticles in the blood stream may induce harmful effects due to undesired interactions with blood components. Thus, there is an emerging need to understand the impact of these nanoagents when meeting blood proteins. In this work, the influence of nanoagents on the structure and stability of the most abundant blood protein, human serum albumin, is presented. Synchrotron radiation circular dichroism showed that AGuIX(®) does not bind to the protein, even at the high ratio of 45 nanoparticles per protein at 3 mg/L. However, it increases the stability of the albumin. Isothermal thermodynamic calorimetry and fluorescence emission spectroscopy demonstrated that the effect is due to preferential hydration processes. Thus, this study confirms that intravenous injection of AGuIX(®) presents limited risks of perturbing the blood stream. In a wider view, the methodology developed in this work may be applied to rapidly evaluate the impact and risk of other nano-products that could come into contact with the bloodstream. MDPI 2020-06-30 /pmc/articles/PMC7369717/ /pubmed/32630060 http://dx.doi.org/10.3390/ijms21134673 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yang, Xiaomin
Bolsa-Ferruz, Marta
Marichal, Laurent
Porcel, Erika
Salado-Leza, Daniela
Lux, François
Tillement, Olivier
Renault, Jean-Philippe
Pin, Serge
Wien, Frank
Lacombe, Sandrine
Human Serum Albumin in the Presence of AGuIX Nanoagents: Structure Stabilisation without Direct Interaction
title Human Serum Albumin in the Presence of AGuIX Nanoagents: Structure Stabilisation without Direct Interaction
title_full Human Serum Albumin in the Presence of AGuIX Nanoagents: Structure Stabilisation without Direct Interaction
title_fullStr Human Serum Albumin in the Presence of AGuIX Nanoagents: Structure Stabilisation without Direct Interaction
title_full_unstemmed Human Serum Albumin in the Presence of AGuIX Nanoagents: Structure Stabilisation without Direct Interaction
title_short Human Serum Albumin in the Presence of AGuIX Nanoagents: Structure Stabilisation without Direct Interaction
title_sort human serum albumin in the presence of aguix nanoagents: structure stabilisation without direct interaction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7369717/
https://www.ncbi.nlm.nih.gov/pubmed/32630060
http://dx.doi.org/10.3390/ijms21134673
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