Chelator-free synthesis of a dual-modality PET/MRI agent.
Chelator-free synthesis of a dual-modality PET/MRI agent.
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DOI:
10.1002/anie.201306306
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发表时间:
2013-12-09
影响因子:
16.6
通讯作者:
Cai, Weibo
中科院分区:
文献类型:
--
作者:
Chen, Feng;Ellison, Paul A.;Lewis, Christina M.;Hong, Hao;Zhang, Yin;Shi, Sixiang;Hernandez, Reinier;Meyerand, M. Elizabeth;Barnhart, Todd E.;Cai, Weibo
Most of the radiometals with physical properties suitable for imaging and/or therapy applications (eg 64Cu, 89Zr, 99mTc, 111In, 177Lu, 90Y, etc.) require the coordination of certain chelators to form stable complexes.[1] Due to the uniqueness of each radionuclide, knowing the particular coordination chemistry and selecting the best chelator with sufficient in vivo stability are a vital, however, highly challenging task. Therefore, the development of a stable radiopharmaceutical that contains both diagnostic and therapeutic radioisotopes, labeled via a simple but effective chelator-free strategy, is highly desirable.
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