N-[ 18F]fluoroethyl-4-piperidyl acetate ([ 18F]FEtP4A) : A PET tracer for imaging brain acetylcholinesterase in vivo
N-[ 18F]Fluoroethyl-4-piperidyl acetate ([ 18F]FEtP4A) was synthesized and evaluated as a PET tracer for imaging brain acetylcholinesterase (AchE) in vivo. [ 18F]FEtP4A was previously prepared by reacting 4-piperidyl acetate (P4A) with 2-[ 18F]fluoroethyl bromide ([ 18F]FEtBr) at 130 °C for 30 min i...
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Veröffentlicht in: | Bioorganic & medicinal chemistry 2003-06, Vol.11 (12), p.2519-2527 |
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Zusammenfassung: | N-[
18F]Fluoroethyl-4-piperidyl acetate ([
18F]FEtP4A) was synthesized and evaluated as a PET tracer for imaging brain acetylcholinesterase (AchE) in vivo. [
18F]FEtP4A was previously prepared by reacting 4-piperidyl acetate (P4A) with 2-[
18F]fluoroethyl bromide ([
18F]FEtBr) at 130
°C for 30
min in 37% radiochemical yield using an automated synthetic system. In this work, [
18F]FEtP4A was synthesized by reacting P4A with 2-[
18F]fluoroethyl iodide ([
18F]FEtI) or 2-[
18F]fluoroethyl triflate ([
18F]FEtOTf in improved radiochemical yields, compared with [
18F]FEtBr under the corresponding condition. Ex vivo autoradiogram of rat brain and PET summation image of monkey brain after iv injection of [
18F]FEtP4A displayed a high radioactivity in the striatum, a region with the highest AchE activity in the brain. Moreover, the distribution pattern of
18F radioactivity was consistent with that of AchE in the brain: striatum>frontal cortex>cerebellum. In the rat and monkey plasma, two radioactive metabolites were detected. However, their presence might not preclude the imaging studies for AchE in the brain, because they were too hydrophilic to pass the blood–brain barrier and to enter the brain. In the rat brain, only [
18F]fluoroethyl-4-piperidinol ([
18F]FEtP4OH) was detected at 30
min postinjection. The hydrolytic [
18F]FEtP4OH displayed a slow washout and a long retention in the monkey brain until the PET experiment (120
min). Although [
18F]FEtP4A is a potential PET tracer for imaging AchE in vivo, its lower hydrolytic rate and lower specificity for AchE than those of [
11C]MP4A may limit its usefulness for the quantitative measurement for AchE in the primate brain.
[
18F]FEtP4A, a potential PET tracer for imaging brain acetylcholinesterase (AchE) in vivo, was synthesized by the respective reaction of P4A with [
18F]FEtBr, [
18F]FEtBr/NaI and [
18F]FEtOTf. After iv injection of [
18F]FEtP4A into animals, ex vivo autoradiogram of rat brain and PET image of monkey brain displayed a significant radioactivity in the striatum, the region with the highest AchE activity in the brain. |
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ISSN: | 0968-0896 1464-3391 |
DOI: | 10.1016/S0968-0896(03)00177-9 |