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Integrity of lipid nanocarriers in bloodstream and tumor quantified by near-infrared ratiometric FRET imaging in living mice

Lipid nanocarriers are considered as promising candidates for drug delivery and cancer targeting because of their low toxicity, biodegradability and capacity to encapsulate drugs and/or contrasting agents. However, their biomedical applications are currently limited because of a poor understanding o...

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Autores principales: Bouchaala, Redouane, Mercier, Luc, Andreiuk, Bohdan, Mély, Yves, Vandamme, Thierry, Anton, Nicolas, Goetz, Jacky G., Klymchenko, Andrey S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Publishers 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968657/
https://www.ncbi.nlm.nih.gov/pubmed/27327767
http://dx.doi.org/10.1016/j.jconrel.2016.06.027
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author Bouchaala, Redouane
Mercier, Luc
Andreiuk, Bohdan
Mély, Yves
Vandamme, Thierry
Anton, Nicolas
Goetz, Jacky G.
Klymchenko, Andrey S.
author_facet Bouchaala, Redouane
Mercier, Luc
Andreiuk, Bohdan
Mély, Yves
Vandamme, Thierry
Anton, Nicolas
Goetz, Jacky G.
Klymchenko, Andrey S.
author_sort Bouchaala, Redouane
collection PubMed
description Lipid nanocarriers are considered as promising candidates for drug delivery and cancer targeting because of their low toxicity, biodegradability and capacity to encapsulate drugs and/or contrasting agents. However, their biomedical applications are currently limited because of a poor understanding of their integrity in vivo. To address this problem, we report on fluorescent nano-emulsion droplets of 100 nm size encapsulating lipophilic near-infrared cyanine 5.5 and 7.5 dyes with a help of bulky hydrophobic counterion tetraphenylborate. Excellent brightness and efficient Förster Resonance Energy Transfer (FRET) inside lipid NCs enabled for the first time quantitative fluorescence ratiometric imaging of NCs integrity directly in the blood circulation, liver and tumor xenografts of living mice using a whole-animal imaging set-up. This unique methodology revealed that the integrity of our FRET NCs in the blood circulation of healthy mice is preserved at 93% at 6 h of post-administration, while it drops to 66% in the liver (half-life is 8.2 h). Moreover, these NCs show fast and efficient accumulation in tumors, where they enter in nearly intact form (77% integrity at 2 h) before losing their integrity to 40% at 6 h (half-life is 4.4 h). Thus, we propose a simple and robust methodology based on ratiometric FRET imaging in vivo to evaluate quantitatively nanocarrier integrity in small animals. We also demonstrate that nano-emulsion droplets are remarkably stable nano-objects that remain nearly intact in the blood circulation and release their content mainly after entering tumors.
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spelling pubmed-49686572016-08-28 Integrity of lipid nanocarriers in bloodstream and tumor quantified by near-infrared ratiometric FRET imaging in living mice Bouchaala, Redouane Mercier, Luc Andreiuk, Bohdan Mély, Yves Vandamme, Thierry Anton, Nicolas Goetz, Jacky G. Klymchenko, Andrey S. J Control Release Article Lipid nanocarriers are considered as promising candidates for drug delivery and cancer targeting because of their low toxicity, biodegradability and capacity to encapsulate drugs and/or contrasting agents. However, their biomedical applications are currently limited because of a poor understanding of their integrity in vivo. To address this problem, we report on fluorescent nano-emulsion droplets of 100 nm size encapsulating lipophilic near-infrared cyanine 5.5 and 7.5 dyes with a help of bulky hydrophobic counterion tetraphenylborate. Excellent brightness and efficient Förster Resonance Energy Transfer (FRET) inside lipid NCs enabled for the first time quantitative fluorescence ratiometric imaging of NCs integrity directly in the blood circulation, liver and tumor xenografts of living mice using a whole-animal imaging set-up. This unique methodology revealed that the integrity of our FRET NCs in the blood circulation of healthy mice is preserved at 93% at 6 h of post-administration, while it drops to 66% in the liver (half-life is 8.2 h). Moreover, these NCs show fast and efficient accumulation in tumors, where they enter in nearly intact form (77% integrity at 2 h) before losing their integrity to 40% at 6 h (half-life is 4.4 h). Thus, we propose a simple and robust methodology based on ratiometric FRET imaging in vivo to evaluate quantitatively nanocarrier integrity in small animals. We also demonstrate that nano-emulsion droplets are remarkably stable nano-objects that remain nearly intact in the blood circulation and release their content mainly after entering tumors. Elsevier Science Publishers 2016-08-28 /pmc/articles/PMC4968657/ /pubmed/27327767 http://dx.doi.org/10.1016/j.jconrel.2016.06.027 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bouchaala, Redouane
Mercier, Luc
Andreiuk, Bohdan
Mély, Yves
Vandamme, Thierry
Anton, Nicolas
Goetz, Jacky G.
Klymchenko, Andrey S.
Integrity of lipid nanocarriers in bloodstream and tumor quantified by near-infrared ratiometric FRET imaging in living mice
title Integrity of lipid nanocarriers in bloodstream and tumor quantified by near-infrared ratiometric FRET imaging in living mice
title_full Integrity of lipid nanocarriers in bloodstream and tumor quantified by near-infrared ratiometric FRET imaging in living mice
title_fullStr Integrity of lipid nanocarriers in bloodstream and tumor quantified by near-infrared ratiometric FRET imaging in living mice
title_full_unstemmed Integrity of lipid nanocarriers in bloodstream and tumor quantified by near-infrared ratiometric FRET imaging in living mice
title_short Integrity of lipid nanocarriers in bloodstream and tumor quantified by near-infrared ratiometric FRET imaging in living mice
title_sort integrity of lipid nanocarriers in bloodstream and tumor quantified by near-infrared ratiometric fret imaging in living mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968657/
https://www.ncbi.nlm.nih.gov/pubmed/27327767
http://dx.doi.org/10.1016/j.jconrel.2016.06.027
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