中华核医学杂志
中華覈醫學雜誌
중화핵의학잡지
CHINESE JOURNAL OF NUCLEAR MEDICINE
2009年
3期
185-188
,共4页
张勇平%章英剑%王明伟%袁慧瑜%姚之丰
張勇平%章英劍%王明偉%袁慧瑜%姚之豐
장용평%장영검%왕명위%원혜유%요지봉
乙酸盐%氟放射性同位素%化学合成%自动化%大鼠
乙痠鹽%氟放射性同位素%化學閤成%自動化%大鼠
을산염%불방사성동위소%화학합성%자동화%대서
Acetate%Fluorine radioisotopes%Chemical synthesis%Automation%Rats
目的 建立半衰期较长的18F-氟乙酸盐(FAC)的制备方法.方法 基于Siemens公司的Explora FDG4合成模块,增加3个试剂位和2个电磁阀,改编运行程序,以"两锅法"结合Sep-Pak简易分离柱的使用,完成18F-FAC的自动化合成.对荷W256肝癌大鼠行18F-FAC PET/CT显像.结果 该法合成时间为65 min,化学收率60%(时间校正),产品放化纯>98%.荷瘤大鼠PET显像示,30和120 min肿瘤标准摄取值(SUV)分别为1.37和1.20,肿瘤/前肢肌肉放射性比值分别为2.32和2.55.结论 用改进的Explora FDG4合成模块可以成功制备放化纯较高的18F-FAC.18F-FAC是一种有潜在应用价值的肝癌显像剂.
目的 建立半衰期較長的18F-氟乙痠鹽(FAC)的製備方法.方法 基于Siemens公司的Explora FDG4閤成模塊,增加3箇試劑位和2箇電磁閥,改編運行程序,以"兩鍋法"結閤Sep-Pak簡易分離柱的使用,完成18F-FAC的自動化閤成.對荷W256肝癌大鼠行18F-FAC PET/CT顯像.結果 該法閤成時間為65 min,化學收率60%(時間校正),產品放化純>98%.荷瘤大鼠PET顯像示,30和120 min腫瘤標準攝取值(SUV)分彆為1.37和1.20,腫瘤/前肢肌肉放射性比值分彆為2.32和2.55.結論 用改進的Explora FDG4閤成模塊可以成功製備放化純較高的18F-FAC.18F-FAC是一種有潛在應用價值的肝癌顯像劑.
목적 건립반쇠기교장적18F-불을산염(FAC)적제비방법.방법 기우Siemens공사적Explora FDG4합성모괴,증가3개시제위화2개전자벌,개편운행정서,이"량과법"결합Sep-Pak간역분리주적사용,완성18F-FAC적자동화합성.대하W256간암대서행18F-FAC PET/CT현상.결과 해법합성시간위65 min,화학수솔60%(시간교정),산품방화순>98%.하류대서PET현상시,30화120 min종류표준섭취치(SUV)분별위1.37화1.20,종류/전지기육방사성비치분별위2.32화2.55.결론 용개진적Explora FDG4합성모괴가이성공제비방화순교고적18F-FAC.18F-FAC시일충유잠재응용개치적간암현상제.
Objective PET/CT with 11C-acetate has a high sensitivity for detection of liver cancer and some cancers that arc poorly detected with 18F-fluorodeoxyglueose (FDG). However, the short half-life of 11C nuclide (11C = 20.4 min) limits the general availability of 11C-acetate. 18F-fluoroaeetate (FAC), an analog of acetate, has the advantage with a longer radioactive half-life (18F = 110 min). The aim of the study was to establish a method for preparing 18F-FAC. Methods In this study, a new automated synthesis of vF-FAC based on modified Siemens Explora FDG4 module was carried out by "two pots" reaction. The modified content of synthesis equipment included addition of 2 valves for liquid solution, 3 reagent position and new synthesis PC program. W256 liver tumor cells baring rats underwent 18F-FAC PET/CT imaging. Results The good separation and purity of final production were adopted via Sep-Pak cartridge extraction. The synthesis of 18F-FAC could be completed within 65 min, with about 60% (time calculated) of radio-chemical yield and more than 98% of radiochemicai purity. The standardized uptake value (SUV) of tumor in the rats was 1.37 and 1.20 at 30 and 120 min, the radioactivity ratios of tumor to muscle were 2.32 and 2.55, respectively. Conclusion Automated synthesis of 18F-FAC, a promising tracer for PET imaging of liver cancer, was developed successfully based upon modified Explora FDG4 module with good results.