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1. 上海市第六人民医院,上海,200233
2. 日本群马大学医学部,日本,371-8511
Published:01 May 2001
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[1]袁志斌,富吉腾美,井上登美夫,遠藤啓吾.亲肿瘤显像剂5-~(18)F-Fluorouracil(~(18)F-FU)的标记合成研究[J].核技术,2001(05):425-427.
YUAN Zhibin. The labeling and synthesis study on tumor positive imaging agent 5- (18)F-Fluorouracil (18F-FU)[J]. Nuclear techniques, 2001, (5): 425-427.
用18 F F2 与Uracil的直接标记法合成了 5- 18F -Fluorouracil
探索18F -FU -PET显像对结肠直肠癌肝转移病人化疗前后疗效评价的意义。产品的放射化学纯 >95%
放射性得率为 60 %
pH值为 7
无菌性试验和热源试验均为阴性
这一结果为临床应用提供了保证。
F-Fluorouracil were successfully labeled and synthesized using direct labeling method by 18 F/F 2 and Uracil. It was used for evaluating 18 F-FU-PET imaging for the colorectal carcinoma patients with liver metastases before and after chemotherapy. The radiochemical purity was above 95%
the radiochemical yield was about 60%
pH value was about 7 and both sterility and apyrogenicity test showed negative result. All these results guarantee its potential clinical usage.
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