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Iodine-124 Based Dual Positron Emission Tomography and Fluorescent Labeling Reagents for In Vivo Cell Tracking
Author(s) -
Truc Pham,
Zhi Lu,
Christopher G. Davis,
Chun Li,
Fangfang Sun,
John Maher,
Ran Yan
Publication year - 2020
Publication title -
bioconjugate chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.279
H-Index - 172
eISSN - 1520-4812
pISSN - 1043-1802
DOI - 10.1021/acs.bioconjchem.9b00799
Subject(s) - chemistry , positron emission tomography , in vivo , fluorescence , reagent , radiochemistry , preclinical imaging , tracking (education) , iodine , brain positron emission tomography , nuclear medicine , optics , organic chemistry , physics , medicine , microbiology and biotechnology , biology , psychology , pedagogy
Understanding the in vivo behavior of experimental therapeutic cells is fundamental to their successful development and clinical translation. Iodine-124 has the longest half-life (4.2 days) among the clinically used positron emitters. Consequently, this isotope offers the longest possible tracking time for directly labeled cells using positron emission tomography (PET). Herein, we have radiosynthesized and evaluated two iodine-124/fluorescein-based dual PET and fluorescent labeling reagents, namely 124 I-FIT-Mal and 124 I-FIT-(PhS) 2 Mal for cell surface thiol bioconjugation. 124 I-FIT-(PhS) 2 Mal labeled cells significantly more effectively than 124 I-FIT-Mal. It conjugated to various cell lines in 22%-62% labeling efficiencies with prolonged iodine-124 retention. 124 I-FIT-(PhS) 2 Mal mainly conjugated on the cell membrane, which was confirmed by high-resolution fluorescence imaging. The migration of 124 I-FIT-(PhS) 2 Mal labeled Jurkat cells was visualized in NSG mice with excellent target-to-background contrast using PET/CT over 7 days. These data demonstrate that 124 I-FIT-(PhS) 2 Mal can dynamically track cell migration in vivo using PET/CT over a clinically relevant time frame.

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