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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.
Sottani, Cristina; Grignani, Elena; Cottica, Danilo; Mazzucchelli, Serena; Sevieri, Marta; Chesi, Arianna; Corsi, Fabio; Galfrè, Sarah; Robustelli Della Cuna, Francesco Saverio; Calleri, Enrica.
Afiliação
  • Sottani C; Environmental Research Center, Istituti Clinici Scientifici Maugeri IRCCS, Pavia, Italy.
  • Grignani E; Environmental Research Center, Istituti Clinici Scientifici Maugeri IRCCS, Pavia, Italy.
  • Cottica D; Environmental Research Center, Istituti Clinici Scientifici Maugeri IRCCS, Pavia, Italy.
  • Mazzucchelli S; Nanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Milano University, Milan, Italy.
  • Sevieri M; Nanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Milano University, Milan, Italy.
  • Chesi A; Nanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Milano University, Milan, Italy.
  • Corsi F; Nanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Milano University, Milan, Italy.
  • Galfrè S; Breast Unit, Istituti Clinici Scientifici Maugeri IRCCS, Pavia, Italy.
  • Robustelli Della Cuna FS; Department of Drug Sciences, University of Pavia, Pavia, Italy.
  • Calleri E; Department of Drug Sciences, University of Pavia, Pavia, Italy.
Front Chem ; 9: 784123, 2021.
Article em En | MEDLINE | ID: mdl-35047479
ABSTRACT
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   m / z 753 → m / z 330 and m / z 827 → m / z 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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Chem Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Chem Ano de publicação: 2021 Tipo de documento: Article