米索硝唑
体内分布
肿瘤缺氧
医学
核医学
正电子发射断层摄影术
缺氧(环境)
Pet成像
显像剂
放射治疗
体内
内科学
氧气
化学
生物化学
生物技术
有机化学
体外
生物
作者
David J. Yang,S Wallace,Abdallah Cherif,Chun Li,Matthew Gretzer,E E Kim,Donald A. Podoloff
出处
期刊:Radiology
[Radiological Society of North America]
日期:1995-03-01
卷期号:194 (3): 795-800
被引量:183
标识
DOI:10.1148/radiology.194.3.7862981
摘要
To develop a hydrophilic ligand to image tumor hypoxia at positron emission tomography (PET).Biodistribution of fluorine-18-labeled fluoroerythronitroimidazole (FETNIM) and F-18-labeled fluoromisonidazole (FMISO) was determined at PET and autoradiography in three mammary-tumor-bearing rats. The partition coefficient of FETNIM, FMISO, and misonidazole was determined.Biodistribution of F-18-labeled FETNIM at 1, 2, and 4 hours showed tumor-to-blood ratios of 2.29 +/- 0.599, 2.41 +/- 0.567 and 8.02 +/- 2.420, respectively, and tumor-to-muscle ratios of 0.66 +/- 0.267, 2.11 +/- 0.347, and 5.92 +/- 2.240, respectively. The tumor-to-blood count density ratio with F-18-labeled FETNIM at 4 hours after injection was significantly higher than with F-18-labeled FMISO. Autoradiographs indicated that both agents could help differentiate hypoxic versus necrotic region in the tumor.F-18-labeled FETNIM can help detect tumor hypoxia and is easier to prepare, less costly, and more hydrophilic than F-18-labeled FMISO.
科研通智能强力驱动
Strongly Powered by AbleSci AI