Rhenium and technetium based radiopharmaceuticals: Development and recent advances

被引:93
作者
Juergens, Sophie [1 ]
Herrmann, Wolfgang A. [1 ]
Kuehn, Fritz E. [1 ]
机构
[1] Tech Univ Munich, Catalysis Res Ctr, Chair Inorgan Chem Mol Catalysis, Ernst Otto Fischer Str 1, D-85747 Garching, Germany
关键词
Rhenium; Technetium; Radiopharmaceuticals; Molecular imaging; Targeting; Review; LYMPH-NODE BIOPSY; COORDINATION CHEMISTRY; BREAST-CANCER; TC-99M-MIBI SCINTIMAMMOGRAPHY; IMAGING AGENT; TC COMPLEXES; SENTINEL; DESIGN; SPECT; IDENTIFICATION;
D O I
10.1016/j.jorganchem.2013.07.042
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The higher homologues of group 7 transition metals, namely technetium and rhenium, offer radioisotopes suitable for the application as radiopharmaceuticals. Three generations of radiopharmaceuticals have been applied so far, with two of them reaching clinical application. While the first generation does not display a target specific functionality to bind exclusively to one ( or few) targets, the second generation allows target specific binding. The synthesis, however, is more sophisticated, but allows in principle a "Lego brick" build up of a radioactive moiety, a linker and a binding moiety. The third generation aims at an "all in one approach", an organometallic derivative of a "key", fitting to a specific receptor that also carries the "load" of the radioactive molecule. Although most elegant from design, such molecules are most difficult to develop. With the many available organometallic and inorganic rhenium derivatives, however, at least a much larger variety of specific "second generation" radiopharmaceuticals should be available. (C) 2013 Elsevier B. V. All rights reserved.
引用
收藏
页码:83 / 89
页数:7
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