In Vivo Biodistribution and Lifetime Analysis of Cy5.5-Conjugated Rituximab in Mice Bearing Lymphoid Tumor Xenograft Using Time-Domain Near-Infrared Optical Imaging
Rituximab is a chimeric monoclonal antibody directed against human CD20 antigen, which is expressed on B-cell lymphocytes and on the majority of B-cell lymphoid malignancies. Herein we report the conjugate of rituximab with the near-infrared (NIR) fluorophore Cy5.5 (RI-Cy5.5) as a tool for in vitro,...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
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SAGE Publishing
2008-11-01
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Series: | Molecular Imaging |
Online Access: | https://doi.org/10.2310/7290.2008.00028 |
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author | Stefania Biffi Chiara Garrovo Paolo Macor Claudio Tripodo Sonia Zorzet Erika Secco Francesco Tedesco Vito Lorusso |
author_facet | Stefania Biffi Chiara Garrovo Paolo Macor Claudio Tripodo Sonia Zorzet Erika Secco Francesco Tedesco Vito Lorusso |
author_sort | Stefania Biffi |
collection | DOAJ |
description | Rituximab is a chimeric monoclonal antibody directed against human CD20 antigen, which is expressed on B-cell lymphocytes and on the majority of B-cell lymphoid malignancies. Herein we report the conjugate of rituximab with the near-infrared (NIR) fluorophore Cy5.5 (RI-Cy5.5) as a tool for in vitro, in vivo, and ex vivo NIR time-domain (TD) optical imaging. In vitro, RI-Cy5.5 retained biologic activity and led to elevated cell-associated fluorescence on tumor cells. In vivo, TD optical imaging analysis of RI-Cy5.5 injected into lymphoma-bearing mice revealed a slow tumor uptake and a specific long-lasting persistence of the probe within the tumor. Biodistribution studies after intraperitoneal and endovenous administration were undertaken to evaluate differences in the tumor uptake. RI-Cy5.5 concentration in the organs after intraperitoneal injection was not as high as after endovenous injection. Ex vivo analysis of biologic tissues and organs by both TD optical imaging and immunohistochemistry confirmed the probe distribution, as demonstrated by imaging experiment in vivo, showing that RI-Cy5.5 selectively accumulated in the tumor tissue and major excretion organs. In summary, the study indicates that NIR TD optical imaging is a powerful tool for rituximab-targeting investigation, furthering understanding of its administration outcome in lymphoma treatment. |
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id | doaj.art-e0e9fe7348b44f709a06747c26200f60 |
institution | Directory Open Access Journal |
issn | 1536-0121 |
language | English |
last_indexed | 2025-02-17T08:06:09Z |
publishDate | 2008-11-01 |
publisher | SAGE Publishing |
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series | Molecular Imaging |
spelling | doaj.art-e0e9fe7348b44f709a06747c26200f602025-01-03T00:11:24ZengSAGE PublishingMolecular Imaging1536-01212008-11-01710.2310/7290.2008.0002810.2310_7290.2008.00028In Vivo Biodistribution and Lifetime Analysis of Cy5.5-Conjugated Rituximab in Mice Bearing Lymphoid Tumor Xenograft Using Time-Domain Near-Infrared Optical ImagingStefania BiffiChiara GarrovoPaolo MacorClaudio TripodoSonia ZorzetErika SeccoFrancesco TedescoVito LorussoRituximab is a chimeric monoclonal antibody directed against human CD20 antigen, which is expressed on B-cell lymphocytes and on the majority of B-cell lymphoid malignancies. Herein we report the conjugate of rituximab with the near-infrared (NIR) fluorophore Cy5.5 (RI-Cy5.5) as a tool for in vitro, in vivo, and ex vivo NIR time-domain (TD) optical imaging. In vitro, RI-Cy5.5 retained biologic activity and led to elevated cell-associated fluorescence on tumor cells. In vivo, TD optical imaging analysis of RI-Cy5.5 injected into lymphoma-bearing mice revealed a slow tumor uptake and a specific long-lasting persistence of the probe within the tumor. Biodistribution studies after intraperitoneal and endovenous administration were undertaken to evaluate differences in the tumor uptake. RI-Cy5.5 concentration in the organs after intraperitoneal injection was not as high as after endovenous injection. Ex vivo analysis of biologic tissues and organs by both TD optical imaging and immunohistochemistry confirmed the probe distribution, as demonstrated by imaging experiment in vivo, showing that RI-Cy5.5 selectively accumulated in the tumor tissue and major excretion organs. In summary, the study indicates that NIR TD optical imaging is a powerful tool for rituximab-targeting investigation, furthering understanding of its administration outcome in lymphoma treatment.https://doi.org/10.2310/7290.2008.00028 |
spellingShingle | Stefania Biffi Chiara Garrovo Paolo Macor Claudio Tripodo Sonia Zorzet Erika Secco Francesco Tedesco Vito Lorusso In Vivo Biodistribution and Lifetime Analysis of Cy5.5-Conjugated Rituximab in Mice Bearing Lymphoid Tumor Xenograft Using Time-Domain Near-Infrared Optical Imaging Molecular Imaging |
title | In Vivo Biodistribution and Lifetime Analysis of Cy5.5-Conjugated Rituximab in Mice Bearing Lymphoid Tumor Xenograft Using Time-Domain Near-Infrared Optical Imaging |
title_full | In Vivo Biodistribution and Lifetime Analysis of Cy5.5-Conjugated Rituximab in Mice Bearing Lymphoid Tumor Xenograft Using Time-Domain Near-Infrared Optical Imaging |
title_fullStr | In Vivo Biodistribution and Lifetime Analysis of Cy5.5-Conjugated Rituximab in Mice Bearing Lymphoid Tumor Xenograft Using Time-Domain Near-Infrared Optical Imaging |
title_full_unstemmed | In Vivo Biodistribution and Lifetime Analysis of Cy5.5-Conjugated Rituximab in Mice Bearing Lymphoid Tumor Xenograft Using Time-Domain Near-Infrared Optical Imaging |
title_short | In Vivo Biodistribution and Lifetime Analysis of Cy5.5-Conjugated Rituximab in Mice Bearing Lymphoid Tumor Xenograft Using Time-Domain Near-Infrared Optical Imaging |
title_sort | in vivo biodistribution and lifetime analysis of cy5 5 conjugated rituximab in mice bearing lymphoid tumor xenograft using time domain near infrared optical imaging |
url | https://doi.org/10.2310/7290.2008.00028 |
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