One-step 18F-labeling of peptides for positron emission tomography imaging using the SiFA methodology

被引:69
|
作者
Waengler, Carmen [1 ,2 ]
Niedermoser, Sabrina [2 ,3 ]
Chin, Joshua [4 ]
Orchowski, Katy [4 ]
Schirrmacher, Esther [4 ]
Jurkschat, Klaus [5 ]
Iovkova-Berends, Liuba [5 ]
Kostikov, Alexey P. [4 ]
Schirrmacher, Ralf [4 ]
Waengler, Bjoern [3 ]
机构
[1] Heidelberg Univ, Med Fac Mannheim, Med Res Ctr Mannheim, D-6800 Mannheim, Germany
[2] Univ Munich, Dept Nucl Med, Munich, Germany
[3] Heidelberg Univ, Med Fac Mannheim, Dept Clin Radiol & Nucl Med, D-6800 Mannheim, Germany
[4] McGill Univ, Montreal Neurol Inst, McConnell Brain Imaging Ctr, Montreal, PQ, Canada
[5] TU Univ Dortmund, Lehrstuhl Anorgan Chem 2, Dortmund, Germany
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
SOLID-PHASE SYNTHESIS; PROSTHETIC GROUP; CLICK-CHEMISTRY; LABELING SYNTHON; PET; RADIOTRACERS; BIOMOLECULES; RGD; RADIOSYNTHESIS; ACYLATION;
D O I
10.1038/nprot.2012.109
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Here we present a procedure to label peptides with the positron-emitting radioisotope fluorine-18 (F-18) using the silicon-fluoride acceptor (SiFA) labeling methodology. Positron emission tomography (PET) has gained high importance in noninvasive imaging of various diseases over the past decades, and thus new specific imaging probes for PET imaging, especially those labeled with F-18, because of the advantageous properties of this nuclide, are highly sought after. N-terminally SiFA-modified peptides can be labeled with F-18(-) in one step at room temperature (20-25 degrees C) or below without forming side products, thereby producing satisfactory radiochemical yields of 46 +/- 1.5% (n = 10). The degree of chemoselectivity of the F-18-introduction, which is based on simple isotopic exchange, allows for a facile cartridge-based purification fully devoid of HPLC implementation, thereby yielding peptides with specific activities between 44.4 and 62.9 GBq mu mol(-1) (1,200-1,700 Ci mmol(-1)) within 25 min.
引用
收藏
页码:1946 / 1955
页数:10
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