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Synthesis, Radiolabeling, and Preliminary in vivo Evaluation of [(68)Ga] IPCAT-NOTA as an Imaging Agent for Dopamine Transporter
INTRODUCTION: Novel radiotracer development for imaging dopamine transporters is a subject of interest because although [(99m)Tc]TRODAT-1, [(123)I]β-CIT, and [(123)I]FP-CIT are commercially available; (99)Mo/(99m)Tc generator is in short supply and (123)I production is highly dependent on compact cy...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8216701/ https://www.ncbi.nlm.nih.gov/pubmed/34168430 http://dx.doi.org/10.2147/DDDT.S288600 |
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author | Farn, Shiou-Shiow Chang, Kang-Wei Lin, Wan-Chi Yu, Hung-Man Lin, Kun-Liang Tseng, Yu-Chin Chang, Yu Yu, Chung-Shan Lin, Wuu-Jyh |
author_facet | Farn, Shiou-Shiow Chang, Kang-Wei Lin, Wan-Chi Yu, Hung-Man Lin, Kun-Liang Tseng, Yu-Chin Chang, Yu Yu, Chung-Shan Lin, Wuu-Jyh |
author_sort | Farn, Shiou-Shiow |
collection | PubMed |
description | INTRODUCTION: Novel radiotracer development for imaging dopamine transporters is a subject of interest because although [(99m)Tc]TRODAT-1, [(123)I]β-CIT, and [(123)I]FP-CIT are commercially available; (99)Mo/(99m)Tc generator is in short supply and (123)I production is highly dependent on compact cyclotron. Therefore, we designed a novel positron emission tomography (PET) tracer based on a tropane derivative through C-2 modification to conjugate NOTA for chelating (68)Ga, a radioisotope derived from a (68)Ge/(68)Ga generator. METHODS: IPCAT-NOTA 22 was synthesized and labeled with [(68)Ga]GaCl(4)(−) at room temperature. Biological studies on serum stability, LogP, and in vitro autoradiography (binding assay and competitive assay) were performed. Furthermore, ex vivo autoradiography, biodistribution, and dynamic PET imaging studies were performed in Sprague Dawley rats. RESULTS: [(68)Ga]IPCAT-NOTA 24 obtained had a radiochemical yield of ≥90% and a specific activity of 4.25 MBq/nmol. [(68)Ga]IPCAT-NOTA 24 of 85% radiochemical purity (RCP%) was stable at 37°C for up to 60 minutes in serum with a lipophilicity of 0.88. The specific binding ratio (SBR%) reached 15.8 ± 6.7 at 60 minutes, and the 85% specific uptake could be blocked through co-injection at 100- and 1000-fold of the cold precursor in in vitro binding studies. Tissue regional distribution studies in rats with [(68)Ga]IPCAT-NOTA 24 showed striatal uptake (0.02% at 5 minutes and 0.007% at 60 minutes) with SBR% of 6%, 25%, and 62% at 5–15, 30–40, and 60–70 minutes, respectively, in NanoPET studies. The RCP% of [(68)Ga]IPCAT-NOTA 24 at 30 minutes in vivo remained 67.65%. CONCLUSION: Data described here provide new information on the design of PET probe of conjugate/pendent approach for DAT imaging. Another chelator or another direct method of intracranial injection must be used to prove the relation between [(68)Ga]IPCAT-NOTA 24 uptake and transporter localization. |
format | Online Article Text |
id | pubmed-8216701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-82167012021-06-23 Synthesis, Radiolabeling, and Preliminary in vivo Evaluation of [(68)Ga] IPCAT-NOTA as an Imaging Agent for Dopamine Transporter Farn, Shiou-Shiow Chang, Kang-Wei Lin, Wan-Chi Yu, Hung-Man Lin, Kun-Liang Tseng, Yu-Chin Chang, Yu Yu, Chung-Shan Lin, Wuu-Jyh Drug Des Devel Ther Original Research INTRODUCTION: Novel radiotracer development for imaging dopamine transporters is a subject of interest because although [(99m)Tc]TRODAT-1, [(123)I]β-CIT, and [(123)I]FP-CIT are commercially available; (99)Mo/(99m)Tc generator is in short supply and (123)I production is highly dependent on compact cyclotron. Therefore, we designed a novel positron emission tomography (PET) tracer based on a tropane derivative through C-2 modification to conjugate NOTA for chelating (68)Ga, a radioisotope derived from a (68)Ge/(68)Ga generator. METHODS: IPCAT-NOTA 22 was synthesized and labeled with [(68)Ga]GaCl(4)(−) at room temperature. Biological studies on serum stability, LogP, and in vitro autoradiography (binding assay and competitive assay) were performed. Furthermore, ex vivo autoradiography, biodistribution, and dynamic PET imaging studies were performed in Sprague Dawley rats. RESULTS: [(68)Ga]IPCAT-NOTA 24 obtained had a radiochemical yield of ≥90% and a specific activity of 4.25 MBq/nmol. [(68)Ga]IPCAT-NOTA 24 of 85% radiochemical purity (RCP%) was stable at 37°C for up to 60 minutes in serum with a lipophilicity of 0.88. The specific binding ratio (SBR%) reached 15.8 ± 6.7 at 60 minutes, and the 85% specific uptake could be blocked through co-injection at 100- and 1000-fold of the cold precursor in in vitro binding studies. Tissue regional distribution studies in rats with [(68)Ga]IPCAT-NOTA 24 showed striatal uptake (0.02% at 5 minutes and 0.007% at 60 minutes) with SBR% of 6%, 25%, and 62% at 5–15, 30–40, and 60–70 minutes, respectively, in NanoPET studies. The RCP% of [(68)Ga]IPCAT-NOTA 24 at 30 minutes in vivo remained 67.65%. CONCLUSION: Data described here provide new information on the design of PET probe of conjugate/pendent approach for DAT imaging. Another chelator or another direct method of intracranial injection must be used to prove the relation between [(68)Ga]IPCAT-NOTA 24 uptake and transporter localization. Dove 2021-06-17 /pmc/articles/PMC8216701/ /pubmed/34168430 http://dx.doi.org/10.2147/DDDT.S288600 Text en © 2021 Farn et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Farn, Shiou-Shiow Chang, Kang-Wei Lin, Wan-Chi Yu, Hung-Man Lin, Kun-Liang Tseng, Yu-Chin Chang, Yu Yu, Chung-Shan Lin, Wuu-Jyh Synthesis, Radiolabeling, and Preliminary in vivo Evaluation of [(68)Ga] IPCAT-NOTA as an Imaging Agent for Dopamine Transporter |
title | Synthesis, Radiolabeling, and Preliminary in vivo Evaluation of [(68)Ga] IPCAT-NOTA as an Imaging Agent for Dopamine Transporter |
title_full | Synthesis, Radiolabeling, and Preliminary in vivo Evaluation of [(68)Ga] IPCAT-NOTA as an Imaging Agent for Dopamine Transporter |
title_fullStr | Synthesis, Radiolabeling, and Preliminary in vivo Evaluation of [(68)Ga] IPCAT-NOTA as an Imaging Agent for Dopamine Transporter |
title_full_unstemmed | Synthesis, Radiolabeling, and Preliminary in vivo Evaluation of [(68)Ga] IPCAT-NOTA as an Imaging Agent for Dopamine Transporter |
title_short | Synthesis, Radiolabeling, and Preliminary in vivo Evaluation of [(68)Ga] IPCAT-NOTA as an Imaging Agent for Dopamine Transporter |
title_sort | synthesis, radiolabeling, and preliminary in vivo evaluation of [(68)ga] ipcat-nota as an imaging agent for dopamine transporter |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8216701/ https://www.ncbi.nlm.nih.gov/pubmed/34168430 http://dx.doi.org/10.2147/DDDT.S288600 |
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