A New Preclinical Decision Support System Based on PET Radiomics: A Preliminary Study on the Evaluation of an Innovative <sup>64</sup>Cu-Labeled Chelator in Mouse Models

The <sup>64</sup>Cu-labeled chelator was analyzed in vivo by positron emission tomography (PET) imaging to evaluate its biodistribution in a murine model at different acquisition times. For this purpose, nine 6-week-old female Balb/C nude strain mice underwent micro-PET imaging at three...

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Main Authors: Viviana Benfante, Alessandro Stefano, Albert Comelli, Paolo Giaccone, Francesco Paolo Cammarata, Selene Richiusa, Fabrizio Scopelliti, Marco Pometti, Milene Ficarra, Sebastiano Cosentino, Marcello Lunardon, Francesca Mastrotto, Alberto Andrighetto, Antonino Tuttolomondo, Rosalba Parenti, Massimo Ippolito, Giorgio Russo
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Journal of Imaging
Subjects:
Online Access:https://www.mdpi.com/2313-433X/8/4/92
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author Viviana Benfante
Alessandro Stefano
Albert Comelli
Paolo Giaccone
Francesco Paolo Cammarata
Selene Richiusa
Fabrizio Scopelliti
Marco Pometti
Milene Ficarra
Sebastiano Cosentino
Marcello Lunardon
Francesca Mastrotto
Alberto Andrighetto
Antonino Tuttolomondo
Rosalba Parenti
Massimo Ippolito
Giorgio Russo
author_facet Viviana Benfante
Alessandro Stefano
Albert Comelli
Paolo Giaccone
Francesco Paolo Cammarata
Selene Richiusa
Fabrizio Scopelliti
Marco Pometti
Milene Ficarra
Sebastiano Cosentino
Marcello Lunardon
Francesca Mastrotto
Alberto Andrighetto
Antonino Tuttolomondo
Rosalba Parenti
Massimo Ippolito
Giorgio Russo
author_sort Viviana Benfante
collection DOAJ
description The <sup>64</sup>Cu-labeled chelator was analyzed in vivo by positron emission tomography (PET) imaging to evaluate its biodistribution in a murine model at different acquisition times. For this purpose, nine 6-week-old female Balb/C nude strain mice underwent micro-PET imaging at three different time points after <sup>64</sup>Cu-labeled chelator injection. Specifically, the mice were divided into group 1 (acquisition 1 h after [<sup>64</sup>Cu] chelator administration, n = 3 mice), group 2 (acquisition 4 h after [<sup>64</sup>Cu]chelator administration, n = 3 mice), and group 3 (acquisition 24 h after [<sup>64</sup>Cu] chelator administration, n = 3 mice). Successively, all PET studies were segmented by means of registration with a standard template space (3D whole-body Digimouse atlas), and 108 radiomics features were extracted from seven organs (namely, heart, bladder, stomach, liver, spleen, kidney, and lung) to investigate possible changes over time in [<sup>64</sup>Cu]chelator biodistribution. The one-way analysis of variance and post hoc Tukey Honestly Significant Difference test revealed that, while heart, stomach, spleen, kidney, and lung districts showed a very low percentage of radiomics features with significant variations (<i>p</i>-value < 0.05) among the three groups of mice, a large number of features (greater than 60% and 50%, respectively) that varied significantly between groups were observed in bladder and liver, indicating a different in vivo uptake of the <sup>64</sup>Cu-labeled chelator over time. The proposed methodology may improve the method of calculating the [<sup>64</sup>Cu]chelator biodistribution and open the way towards a decision support system in the field of new radiopharmaceuticals used in preclinical imaging trials.
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spelling doaj.art-5e202ac6c9674075854c81b05b6634942023-12-01T21:07:34ZengMDPI AGJournal of Imaging2313-433X2022-03-01849210.3390/jimaging8040092A New Preclinical Decision Support System Based on PET Radiomics: A Preliminary Study on the Evaluation of an Innovative <sup>64</sup>Cu-Labeled Chelator in Mouse ModelsViviana Benfante0Alessandro Stefano1Albert Comelli2Paolo Giaccone3Francesco Paolo Cammarata4Selene Richiusa5Fabrizio Scopelliti6Marco Pometti7Milene Ficarra8Sebastiano Cosentino9Marcello Lunardon10Francesca Mastrotto11Alberto Andrighetto12Antonino Tuttolomondo13Rosalba Parenti14Massimo Ippolito15Giorgio Russo16Institute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), 90015 Cefalù, ItalyInstitute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), 90015 Cefalù, ItalyRi.MED Foundation, Via Bandiera 11, 90133 Palermo, ItalyRi.MED Foundation, Via Bandiera 11, 90133 Palermo, ItalyInstitute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), 90015 Cefalù, ItalyInstitute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), 90015 Cefalù, ItalyNuclear Medicine Department, Cannizzaro Hospital, 95126 Catania, ItalyNuclear Medicine Department, Cannizzaro Hospital, 95126 Catania, ItalyInstitute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), 90015 Cefalù, ItalyNuclear Medicine Department, Cannizzaro Hospital, 95126 Catania, ItalyDepartment of Physics and Astronomy, University of Padova, 35131 Padova, ItalyDepartment of Pharmaceutical and Pharamacological Sciences, University of Padova, 35131 Padova, ItalyLegnaro National Laboratories, National Institute of Nuclear Physics, 35020 Legnaro, ItalyDepartment of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, Molecular and Clinical Medicine, University of Palermo, 90127 Palermo, ItalyDepartment of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, ItalyNuclear Medicine Department, Cannizzaro Hospital, 95126 Catania, ItalyInstitute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), 90015 Cefalù, ItalyThe <sup>64</sup>Cu-labeled chelator was analyzed in vivo by positron emission tomography (PET) imaging to evaluate its biodistribution in a murine model at different acquisition times. For this purpose, nine 6-week-old female Balb/C nude strain mice underwent micro-PET imaging at three different time points after <sup>64</sup>Cu-labeled chelator injection. Specifically, the mice were divided into group 1 (acquisition 1 h after [<sup>64</sup>Cu] chelator administration, n = 3 mice), group 2 (acquisition 4 h after [<sup>64</sup>Cu]chelator administration, n = 3 mice), and group 3 (acquisition 24 h after [<sup>64</sup>Cu] chelator administration, n = 3 mice). Successively, all PET studies were segmented by means of registration with a standard template space (3D whole-body Digimouse atlas), and 108 radiomics features were extracted from seven organs (namely, heart, bladder, stomach, liver, spleen, kidney, and lung) to investigate possible changes over time in [<sup>64</sup>Cu]chelator biodistribution. The one-way analysis of variance and post hoc Tukey Honestly Significant Difference test revealed that, while heart, stomach, spleen, kidney, and lung districts showed a very low percentage of radiomics features with significant variations (<i>p</i>-value < 0.05) among the three groups of mice, a large number of features (greater than 60% and 50%, respectively) that varied significantly between groups were observed in bladder and liver, indicating a different in vivo uptake of the <sup>64</sup>Cu-labeled chelator over time. The proposed methodology may improve the method of calculating the [<sup>64</sup>Cu]chelator biodistribution and open the way towards a decision support system in the field of new radiopharmaceuticals used in preclinical imaging trials.https://www.mdpi.com/2313-433X/8/4/92radiomicsmicro-PET/CTmouse imagingatlas<sup>64</sup>Cu-labeled chelator
spellingShingle Viviana Benfante
Alessandro Stefano
Albert Comelli
Paolo Giaccone
Francesco Paolo Cammarata
Selene Richiusa
Fabrizio Scopelliti
Marco Pometti
Milene Ficarra
Sebastiano Cosentino
Marcello Lunardon
Francesca Mastrotto
Alberto Andrighetto
Antonino Tuttolomondo
Rosalba Parenti
Massimo Ippolito
Giorgio Russo
A New Preclinical Decision Support System Based on PET Radiomics: A Preliminary Study on the Evaluation of an Innovative <sup>64</sup>Cu-Labeled Chelator in Mouse Models
Journal of Imaging
radiomics
micro-PET/CT
mouse imaging
atlas
<sup>64</sup>Cu-labeled chelator
title A New Preclinical Decision Support System Based on PET Radiomics: A Preliminary Study on the Evaluation of an Innovative <sup>64</sup>Cu-Labeled Chelator in Mouse Models
title_full A New Preclinical Decision Support System Based on PET Radiomics: A Preliminary Study on the Evaluation of an Innovative <sup>64</sup>Cu-Labeled Chelator in Mouse Models
title_fullStr A New Preclinical Decision Support System Based on PET Radiomics: A Preliminary Study on the Evaluation of an Innovative <sup>64</sup>Cu-Labeled Chelator in Mouse Models
title_full_unstemmed A New Preclinical Decision Support System Based on PET Radiomics: A Preliminary Study on the Evaluation of an Innovative <sup>64</sup>Cu-Labeled Chelator in Mouse Models
title_short A New Preclinical Decision Support System Based on PET Radiomics: A Preliminary Study on the Evaluation of an Innovative <sup>64</sup>Cu-Labeled Chelator in Mouse Models
title_sort new preclinical decision support system based on pet radiomics a preliminary study on the evaluation of an innovative sup 64 sup cu labeled chelator in mouse models
topic radiomics
micro-PET/CT
mouse imaging
atlas
<sup>64</sup>Cu-labeled chelator
url https://www.mdpi.com/2313-433X/8/4/92
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