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Synthesis of PET tracers for imaging of thiocyanate efflux from the brain
https://repo.qst.go.jp/records/86456
https://repo.qst.go.jp/records/8645689861ea0-45a7-49e4-b9cc-976499c74fab
| Item type | 会議発表論文 / Conference Paper(1) | |||||
|---|---|---|---|---|---|---|
| 公開日 | 2022-04-27 | |||||
| タイトル | ||||||
| タイトル | Synthesis of PET tracers for imaging of thiocyanate efflux from the brain | |||||
| 言語 | ||||||
| 言語 | eng | |||||
| 資源タイプ | ||||||
| 資源タイプ識別子 | http://purl.org/coar/resource_type/c_5794 | |||||
| 資源タイプ | conference paper | |||||
| アクセス権 | ||||||
| アクセス権 | metadata only access | |||||
| アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
| 著者 |
Toshimitsu, Okamura
× Toshimitsu, Okamura× Masanao, Ogawa× Tatsuya, Kikuchi× Zhang, Ming-Rong× Toshimitsu, Okamura× Masanao, Ogawa× Tatsuya, Kikuchi× Zhang, Ming-Rong |
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| 抄録 | ||||||
| 内容記述タイプ | Abstract | |||||
| 内容記述 | Objectives There exist carrier-mediated systems for actively transporting thiocyanate from the brain to the blood, causing the low concentration of thiocyanate in the brain in addition to the limited permeability of the blood-brain barrier. Evaluation of the in vivo efflux of thiocyanate will contribute to elucidating the physiological and biological implication of the efflux systems in the brain. However, the currently available methods are limited to invasive evaluation by microinjection of radioactive thiocyanate into the brain. Here, we present the radiosynthesis of the organic [11C]thiocyanates for imaging thiocyanate efflux from the brain. Based on the metabolite extrusion method [1], we designed candidate protracers: methyl [11C]thiocyanate ([11C]MeT), benzyl [11C]thiocyanate ([11C]BnT), phenyl [11C]thiocyanate ([11C]PhT), 2,4-dinitrophenyl [11C]thiocyanate ([11C]DNPT), and 6-[11C]thiocyanatopurine derivative ([11C]TP). Methods The 11C-labeled candidates were synthesized via the reaction of halide-precursor with [11C]thiocyanate or the reaction of disulfide-precursor with [11C]cyanide. All radiochemical yields (RCYs) were determined by radio-HPLC analysis of the crude product. The effects of reaction time, solvents (methanol, acetonitrile, N,N-dimethylformamide, acetone, or tetrahydrofuran), and reaction temperature on RCYs of the 11C-labled candidates were investigated. Results In either acetone, N,N-dimethylformamide, or tetrahydrofuran, methyl iodide reacted with [11C]thiocyanate to provide moderate to high RCY of the product under short-reaction time at 80°C. Thiocyanation of benzyl bromide with[11C]thiocyanate proceeded under the same conditions. By contrast, the conversion of halide-precursors to [11C]Ph, [11C]DNPT, [11C]TP was poor. In the presence of CuSO4, [11C]DNPT and [11C]TP were successfully produced at 150°C in high RCY (80–90%) and moderate RCY (60%), respectively. The conversion to [11C]PhT was still poor in the presence of CuSO4; however, the reaction of the disulfide-precursor with [11C]cyanide provided moderate RCY of [11C]PhT. This reaction also provided [11C]TP in high RCY. Conclusions The candidates, [11C]MeT, [11C]BnT, [11C]PhT, [11C]DNPT, and [11C]TP, were successfully synthesized by either the reaction of halide-precursors with [11C]thiocyanate or disulfide-precursors with [11C]cyanide. Further in vivo studies are in progress. |
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| 書誌情報 |
Nuclear Medicine and Biology 発行日 2022-06 |
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| 出版者 | ||||||
| 出版者 | Elsevier Ltd. | |||||
| ISSN | ||||||
| 収録物識別子タイプ | ISSN | |||||
| 収録物識別子 | 0969-8051 | |||||
