An updated synthesis of [11C]carfentanil for positron emission tomography (PET) imaging of the μ-opioid receptor

被引:16
|
作者
Blecha, Joseph E. [1 ]
Henderson, Bradford D. [2 ]
Hockley, Brian G. [2 ]
VanBrocklin, Henry F. [1 ]
Zubieta, Jon-Kar [3 ]
DaSilva, Alexandre F. [4 ]
Kilbourn, Michael R. [2 ]
Koeppe, Robert A. [2 ]
Scott, Peter J. H. [2 ]
Shao, Xia [2 ]
机构
[1] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, San Francisco, CA 94143 USA
[2] Univ Michigan, Dept Radiol, Med Sch, Ann Arbor, MI 48109 USA
[3] Univ Utah, Dept Psychiat, Univ Neuropsychiat Inst, Hlth Ctr, Salt Lake City, UT USA
[4] Univ Michigan, Sch Dent, Biol & Mat Sci Dept, Headache & Orofacial Pain Effort, Ann Arbor, MI 48109 USA
关键词
C-11; carbon-11; opioid; PET radiochemistry; radiosynthesis; MAJOR DEPRESSION; RESPONSES; NEUROTRANSMISSION; <C-11>CARFENTANIL; RADIOSYNTHESES; CHEMISTRY; BRAIN; WOMEN; PAIN;
D O I
10.1002/jlcr.3513
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
[C-11]Carfentanil ([C-11]CFN) is a selective radiotracer for in vivo positron emission tomography imaging studies of the -opioid system that, in our laboratories, is synthesized by methylation of the corresponding carboxylate precursor with [C-11]MeOTf, and purified using a C2 solid-phase extraction cartridge. Changes in the commercial availability of common C2 cartridges have necessitated future proofing the synthesis of [C-11]CFN to maintain reliable delivery of the radiotracer for clinical imaging studies. An updated synthesis of [C-11]CFN is reported that replaces a now obsolete purification cartridge with a new commercially available version and also substitutes the organic solvents used in traditional production methods with ethanol.
引用
收藏
页码:375 / 380
页数:6
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