Automated radiosynthesis of [11C]L-deprenyl-D2 and [11C]D-deprenyl using a commercial platform

被引:10
|
作者
Buccino, Pablo [1 ]
Kreimerman, Ingrid [1 ]
Zirbesegger, Kevin [1 ]
Porcal, Williams [1 ,2 ]
Savio, Eduardo [1 ,3 ]
Engler, Henry [1 ]
机构
[1] Ctr Uruguayo Imagenol Mol CUDIM, Ricaldoni 2010, Montevideo 11600, Uruguay
[2] Univ Republica, Fac Quim, Dept Quim Organ, Gral Flores 2124, Montevideo 11800, Uruguay
[3] Univ Republica, Fac Quim, Catedra Radioquim, Gral Flores 2124, Montevideo 11800, Uruguay
关键词
C-11]L-deprenyl-D-2; C-11]D-deprenyl; Automated synthesis; PET chemistry; POSITRON-EMISSION-TOMOGRAPHY; MONOAMINE-OXIDASE; L-DEPRENYL; ASTROCYTOSIS; C-11; PET; DISEASE; MULTITRACER;
D O I
10.1016/j.apradiso.2015.12.051
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two C-11-labelled PET tracers, (R)-N-[C-11]methyl-N-(3,3-dideuteropropargyl)-1-phenylpropan-2-amine ([C-11]L-deprenyl-D-2, [C-11]DED) and (S)-N-[C-11]methyl-N-propargyl-1-phenylpropan-2-amine ([C-11]D-deprenyl, [C-11]DDE) were synthesised. One step N-alkylation with [C-11]MeI or [C-11]MeOTf was performed using the automated platform TRACERlab (R) FX-C Pro. The labelled products were obtained with (37 +/- 15)% (n=10) (end of synthesis, decay corrected from [C-11]MeI) radiochemical yields from [C-11]MeI after 38 +/- 3 min synthesis time. In all cases, radiochemical purity was over 99% when [C-11]MeOTf was used. This synthesis using a commercial platform makes these tracers more accessible for clinical research purposes. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:47 / 52
页数:6
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