Rapid 'on-column' preparation of hydrogen [11C]cyanide from [11C]methyl iodide via [11C]formaldehyde

被引:6
|
作者
Kikuchi, Tatsuya [1 ]
Ogawa, Masanao [1 ,2 ]
Okamura, Toshimitsu [1 ]
Gee, Antony D. [3 ]
Zhang, Ming-Rong [1 ]
机构
[1] Natl Inst Quantum Sci & Technol, Inst Quantum Med Sci, Dept Adv Nucl Med Sci, Inage Ku, 4-9-1 Anagawa, Chiba 2638555, Japan
[2] SHI Accelerator Serv Ltd, Shinagawa Ku, 1-17-6 Osaki, Tokyo 1410032, Japan
[3] Kings Coll London, Sch Biomed Engn & Imaging Sci, St Thomas Hosp, 4th Floor Lambeth Wing,Lambeth Palace Rd, London SE1 7EH, England
基金
英国工程与自然科学研究理事会;
关键词
POSITRON-EMISSION-TOMOGRAPHY; C-11; FORMALDEHYDE; N-OXIDE; CONVENIENT REAGENT; CARBON-DIOXIDE; SULFONIC ACID; CONVERSION; CYANATION; ALDEHYDES; QUANTIFICATION;
D O I
10.1039/d1sc07033a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogen [C-11]cyanide ([C-11]HCN) is a versatile C-11-labelling agent for the production of C-11-labelled compounds used for positron emission tomography (PET). However, the traditional method for [C-11]HCN production requires a dedicated infrastructure, limiting accessibility to [C-11]HCN. Herein, we report a simple and efficient [C-11]HCN production method that can be easily implemented in C-11 production facilities. The immediate production of [C-11]HCN was achieved by passing gaseous [C-11]methyl iodide ([C-11]CH3I) through a small two-layered reaction column. The first layer contained an N-oxide and a sulfoxide for conversion of [C-11]CH3I to [C-11]formaldehyde ([C-11]CH2O). The [C-11]CH2O produced was subsequently converted to [C-11]HCN in a second layer containing hydroxylamine-O-sulfonic acid. The yield of [C-11]HCN produced by the current method was comparable to that of [C-11]HCN produced by the traditional method. The use of oxymatrine and diphenyl sulfoxide for [C-11]CH2O production prevented deterioration of the molar activity of [C-11]HCN. Using this method, compounds labelled with [C-11]HCN are now made easily accessible for PET synthesis applications using readily available labware, without the need for the 'traditional' dedicated cyanide synthesis infrastructure.
引用
收藏
页码:3556 / 3562
页数:7
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