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Visualization of biodistribution of Zn complex with antidiabetic activity using semiconductor Compton camera GREI

Various types of zinc (Zn) complexes have been developed as promising antidiabetic agents in recent years. However, the pharmacological action of Zn complex is not elucidated because the biodistribution of the complex in a living organism has not been studied. Nuclear medicine imaging is superior te...

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Autores principales: Munekane, Masayuki, Motomura, Shinji, Kamino, Shinichiro, Ueda, Masashi, Haba, Hiromitsu, Yoshikawa, Yutaka, Yasui, Hiroyuki, Hiromura, Makoto, Enomoto, Shuichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600336/
https://www.ncbi.nlm.nih.gov/pubmed/28955826
http://dx.doi.org/10.1016/j.bbrep.2015.12.004
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author Munekane, Masayuki
Motomura, Shinji
Kamino, Shinichiro
Ueda, Masashi
Haba, Hiromitsu
Yoshikawa, Yutaka
Yasui, Hiroyuki
Hiromura, Makoto
Enomoto, Shuichi
author_facet Munekane, Masayuki
Motomura, Shinji
Kamino, Shinichiro
Ueda, Masashi
Haba, Hiromitsu
Yoshikawa, Yutaka
Yasui, Hiroyuki
Hiromura, Makoto
Enomoto, Shuichi
author_sort Munekane, Masayuki
collection PubMed
description Various types of zinc (Zn) complexes have been developed as promising antidiabetic agents in recent years. However, the pharmacological action of Zn complex is not elucidated because the biodistribution of the complex in a living organism has not been studied. Nuclear medicine imaging is superior technology for the noninvasive analysis of the temporal distribution of drug candidates in living organisms. Gamma-ray emission imaging (GREI), which was developed by our laboratory as a novel molecular imaging modality, was adopted to visualize various γ-ray–emitting radionuclides that are not detected by conventional imaging techniques such as positron emission tomography and single-photon emission computed tomography. Therefore, we applied GREI to a biodistribution assay of Zn complexes. In the present study, (65)Zn was produced in the (nat)Cu(p,n) reaction in an azimuthal varying field cyclotron for the GREI experiment. The distribution was then noninvasively visualized using GREI after the intravenous administration of a (65)Zn-labeled di(1-oxy-2-pyridinethiolato)zinc [Zn(opt)(2)], ZnCl(2), and di(l-histidinato)zinc. The GREI images were validated using conventional invasive assays. This novel study showed that GREI is a powerful tool for the biodistribution analysis of antidiabetic Zn complexes in a living organism. In addition, accumulation of (65)Zn in the cardiac blood pool was observed for [Zn(opt)(2)], which exhibits potent antidiabetic activity. These results suggest that the slow elimination of Zn from the blood is correlated to the antidiabetic activity of [Zn(opt)(2)].
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spelling pubmed-56003362017-09-27 Visualization of biodistribution of Zn complex with antidiabetic activity using semiconductor Compton camera GREI Munekane, Masayuki Motomura, Shinji Kamino, Shinichiro Ueda, Masashi Haba, Hiromitsu Yoshikawa, Yutaka Yasui, Hiroyuki Hiromura, Makoto Enomoto, Shuichi Biochem Biophys Rep Research Article Various types of zinc (Zn) complexes have been developed as promising antidiabetic agents in recent years. However, the pharmacological action of Zn complex is not elucidated because the biodistribution of the complex in a living organism has not been studied. Nuclear medicine imaging is superior technology for the noninvasive analysis of the temporal distribution of drug candidates in living organisms. Gamma-ray emission imaging (GREI), which was developed by our laboratory as a novel molecular imaging modality, was adopted to visualize various γ-ray–emitting radionuclides that are not detected by conventional imaging techniques such as positron emission tomography and single-photon emission computed tomography. Therefore, we applied GREI to a biodistribution assay of Zn complexes. In the present study, (65)Zn was produced in the (nat)Cu(p,n) reaction in an azimuthal varying field cyclotron for the GREI experiment. The distribution was then noninvasively visualized using GREI after the intravenous administration of a (65)Zn-labeled di(1-oxy-2-pyridinethiolato)zinc [Zn(opt)(2)], ZnCl(2), and di(l-histidinato)zinc. The GREI images were validated using conventional invasive assays. This novel study showed that GREI is a powerful tool for the biodistribution analysis of antidiabetic Zn complexes in a living organism. In addition, accumulation of (65)Zn in the cardiac blood pool was observed for [Zn(opt)(2)], which exhibits potent antidiabetic activity. These results suggest that the slow elimination of Zn from the blood is correlated to the antidiabetic activity of [Zn(opt)(2)]. Elsevier 2015-12-08 /pmc/articles/PMC5600336/ /pubmed/28955826 http://dx.doi.org/10.1016/j.bbrep.2015.12.004 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Munekane, Masayuki
Motomura, Shinji
Kamino, Shinichiro
Ueda, Masashi
Haba, Hiromitsu
Yoshikawa, Yutaka
Yasui, Hiroyuki
Hiromura, Makoto
Enomoto, Shuichi
Visualization of biodistribution of Zn complex with antidiabetic activity using semiconductor Compton camera GREI
title Visualization of biodistribution of Zn complex with antidiabetic activity using semiconductor Compton camera GREI
title_full Visualization of biodistribution of Zn complex with antidiabetic activity using semiconductor Compton camera GREI
title_fullStr Visualization of biodistribution of Zn complex with antidiabetic activity using semiconductor Compton camera GREI
title_full_unstemmed Visualization of biodistribution of Zn complex with antidiabetic activity using semiconductor Compton camera GREI
title_short Visualization of biodistribution of Zn complex with antidiabetic activity using semiconductor Compton camera GREI
title_sort visualization of biodistribution of zn complex with antidiabetic activity using semiconductor compton camera grei
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600336/
https://www.ncbi.nlm.nih.gov/pubmed/28955826
http://dx.doi.org/10.1016/j.bbrep.2015.12.004
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