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Development and Validation of a Bioanalytical UHPLC-MS/MS Method Applied to Murine Liver Tissue for the Determination of Indocyanine Green Loaded in H-Ferritin Nanoparticles

Indocyanine green (ICG) is one of the most commonly used fluorophores in near-infrared fluorescence-guided techniques. However, the molecule is prone to form aggregates in saline solution with a limited photostability and a moderate fluorescence yield. ICG was thus formulated using protein-based nan...

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Autores principales: Sottani, Cristina, Grignani, Elena, Cottica, Danilo, Mazzucchelli, Serena, Sevieri, Marta, Chesi, Arianna, Corsi, Fabio, Galfrè, Sarah, Robustelli della Cuna, Francesco Saverio, Calleri, Enrica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762227/
https://www.ncbi.nlm.nih.gov/pubmed/35047479
http://dx.doi.org/10.3389/fchem.2021.784123
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author Sottani, Cristina
Grignani, Elena
Cottica, Danilo
Mazzucchelli, Serena
Sevieri, Marta
Chesi, Arianna
Corsi, Fabio
Galfrè, Sarah
Robustelli della Cuna, Francesco Saverio
Calleri, Enrica
author_facet Sottani, Cristina
Grignani, Elena
Cottica, Danilo
Mazzucchelli, Serena
Sevieri, Marta
Chesi, Arianna
Corsi, Fabio
Galfrè, Sarah
Robustelli della Cuna, Francesco Saverio
Calleri, Enrica
author_sort Sottani, Cristina
collection PubMed
description Indocyanine green (ICG) is one of the most commonly used fluorophores in near-infrared fluorescence-guided techniques. However, the molecule is prone to form aggregates in saline solution with a limited photostability and a moderate fluorescence yield. ICG was thus formulated using protein-based nanoparticles of H-ferritin (HFn) in order to generate a new nanostructure, HFn-ICG. In this study, an ultrahigh performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) system was employed to develop and validate the quantitative analysis of ICG in liver tissue samples from HFn-ICG-treated mice. To precipitate HFn, cold acetone in acidic solution at pH 5.0 was used. The processed liver samples were injected into the UHPLC-MS/MS system for analysis using the positive electrospray ionization mode. Chromatographic separation was achieved on a Waters Acquity UPLC(®) HSS T3 Column (1.8 μm, 2.1 × 100 mm) with 0.1% formic acid and acetonitrile as the mobile phase with gradient elution. The selected reaction monitoring transitions of [Formula: see text] 753 [Formula: see text] 330 and [Formula: see text] 827 [Formula: see text] 330 were applied for ICG and IR-820 (the internal standard, IS), respectively. The method was selective and linear over a concentration range of 50–1,500 ng/ml. The method was validated for sensitivity, accuracy, precision, extraction recovery, matrix effect, and stability in liver tissue homogenates. ICG extraction recoveries ranged between 85 and 108%. The intra- and inter-day precisions were less than 6.28%. The method was applied to a bio-distribution study to compare the amount of ICG levels from mice treated with HFn-ICG and free ICG. The analyses of the homogenate samples from the two types of treatment showed that the concentration levels of ICG is approximately six-fold higher than those of free ICG (1,411 ± 7.62 ng/ml vs. 235 ± 26.0 ng/ml) at 2 h post injection.
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spelling pubmed-87622272022-01-18 Development and Validation of a Bioanalytical UHPLC-MS/MS Method Applied to Murine Liver Tissue for the Determination of Indocyanine Green Loaded in H-Ferritin Nanoparticles Sottani, Cristina Grignani, Elena Cottica, Danilo Mazzucchelli, Serena Sevieri, Marta Chesi, Arianna Corsi, Fabio Galfrè, Sarah Robustelli della Cuna, Francesco Saverio Calleri, Enrica Front Chem Chemistry Indocyanine green (ICG) is one of the most commonly used fluorophores in near-infrared fluorescence-guided techniques. However, the molecule is prone to form aggregates in saline solution with a limited photostability and a moderate fluorescence yield. ICG was thus formulated using protein-based nanoparticles of H-ferritin (HFn) in order to generate a new nanostructure, HFn-ICG. In this study, an ultrahigh performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) system was employed to develop and validate the quantitative analysis of ICG in liver tissue samples from HFn-ICG-treated mice. To precipitate HFn, cold acetone in acidic solution at pH 5.0 was used. The processed liver samples were injected into the UHPLC-MS/MS system for analysis using the positive electrospray ionization mode. Chromatographic separation was achieved on a Waters Acquity UPLC(®) HSS T3 Column (1.8 μm, 2.1 × 100 mm) with 0.1% formic acid and acetonitrile as the mobile phase with gradient elution. The selected reaction monitoring transitions of [Formula: see text] 753 [Formula: see text] 330 and [Formula: see text] 827 [Formula: see text] 330 were applied for ICG and IR-820 (the internal standard, IS), respectively. The method was selective and linear over a concentration range of 50–1,500 ng/ml. The method was validated for sensitivity, accuracy, precision, extraction recovery, matrix effect, and stability in liver tissue homogenates. ICG extraction recoveries ranged between 85 and 108%. The intra- and inter-day precisions were less than 6.28%. The method was applied to a bio-distribution study to compare the amount of ICG levels from mice treated with HFn-ICG and free ICG. The analyses of the homogenate samples from the two types of treatment showed that the concentration levels of ICG is approximately six-fold higher than those of free ICG (1,411 ± 7.62 ng/ml vs. 235 ± 26.0 ng/ml) at 2 h post injection. Frontiers Media S.A. 2022-01-03 /pmc/articles/PMC8762227/ /pubmed/35047479 http://dx.doi.org/10.3389/fchem.2021.784123 Text en Copyright © 2022 Sottani, Grignani, Cottica, Mazzucchelli, Sevieri, Chesi, Corsi, Galfrè, Robustelli della Cuna and Calleri. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Sottani, Cristina
Grignani, Elena
Cottica, Danilo
Mazzucchelli, Serena
Sevieri, Marta
Chesi, Arianna
Corsi, Fabio
Galfrè, Sarah
Robustelli della Cuna, Francesco Saverio
Calleri, Enrica
Development and Validation of a Bioanalytical UHPLC-MS/MS Method Applied to Murine Liver Tissue for the Determination of Indocyanine Green Loaded in H-Ferritin Nanoparticles
title Development and Validation of a Bioanalytical UHPLC-MS/MS Method Applied to Murine Liver Tissue for the Determination of Indocyanine Green Loaded in H-Ferritin Nanoparticles
title_full Development and Validation of a Bioanalytical UHPLC-MS/MS Method Applied to Murine Liver Tissue for the Determination of Indocyanine Green Loaded in H-Ferritin Nanoparticles
title_fullStr Development and Validation of a Bioanalytical UHPLC-MS/MS Method Applied to Murine Liver Tissue for the Determination of Indocyanine Green Loaded in H-Ferritin Nanoparticles
title_full_unstemmed Development and Validation of a Bioanalytical UHPLC-MS/MS Method Applied to Murine Liver Tissue for the Determination of Indocyanine Green Loaded in H-Ferritin Nanoparticles
title_short Development and Validation of a Bioanalytical UHPLC-MS/MS Method Applied to Murine Liver Tissue for the Determination of Indocyanine Green Loaded in H-Ferritin Nanoparticles
title_sort development and validation of a bioanalytical uhplc-ms/ms method applied to murine liver tissue for the determination of indocyanine green loaded in h-ferritin nanoparticles
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762227/
https://www.ncbi.nlm.nih.gov/pubmed/35047479
http://dx.doi.org/10.3389/fchem.2021.784123
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