An efficient preparation of labelling precursor of [11C]L-deprenyl-D2 and automated radiosynthesis
Abstract Background The synthesis of [11C]L-deprenyl-D2 for imaging of astrocytosis with positron emission tomography (PET) in neurodegenerative diseases has been previously reported. [11C]L-deprenyl-D2 radiosynthesis requires a precursor, L-nordeprenyl-D2, which has been previously synthesized from...
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doaj-9c1919586b28484f858b10cf50efb6472020-11-24T21:36:19ZengSpringerOpenEJNMMI Radiopharmacy and Chemistry2365-421X2017-07-012111210.1186/s41181-017-0029-5An efficient preparation of labelling precursor of [11C]L-deprenyl-D2 and automated radiosynthesisKevin Zirbesegger0Pablo Buccino1Ingrid Kreimerman2Henry Engler3Williams Porcal4Eduardo Savio5Centro Uruguayo de Imagenología Molecular (CUDIM)Centro Uruguayo de Imagenología Molecular (CUDIM)Centro Uruguayo de Imagenología Molecular (CUDIM)Centro Uruguayo de Imagenología Molecular (CUDIM)Centro Uruguayo de Imagenología Molecular (CUDIM)Centro Uruguayo de Imagenología Molecular (CUDIM)Abstract Background The synthesis of [11C]L-deprenyl-D2 for imaging of astrocytosis with positron emission tomography (PET) in neurodegenerative diseases has been previously reported. [11C]L-deprenyl-D2 radiosynthesis requires a precursor, L-nordeprenyl-D2, which has been previously synthesized from L-amphetamine as starting material with low overall yields. Here, we present an efficient synthesis of L-nordeprenyl-D2 organic precursor as free base and automated radiosynthesis of [11C]L-deprenyl-D2 for PET imaging of astrocytosis. The L-nordeprenyl-D2 precursor was synthesized from the easily commercial available and cheap reagent L-phenylalanine in five steps. Next, N-alkylation of L-nordeprenyl-D2 free base with [11C]MeOTf was optimized using the automated commercial platform GE TRACERlab® FX C Pro. Results A simple and efficient synthesis of L-nordeprenyl-D2 precursor of [11C]L-deprenyl-D2 as free base has been developed in five synthetic steps with an overall yield of 33%. The precursor as free base has been stable for 9 months stored at low temperature (−20 °C). The labelled product was obtained with 44 ± 13% (n = 12) (end of synthesis, decay corrected) radiochemical yield from [11C]MeI after 35 min synthesis time. The radiochemical purity was over 99% in all cases and specific activity was (170 ± 116) GBq/μmol. Conclusions A high-yield synthesis of [11C]L-deprenyl-D2 has been achieved with high purity and specific activity. L-nordeprenyl-D2 precursor as free amine was applicable for automated production in a commercial synthesis module for preclinical and clinical application.http://link.springer.com/article/10.1186/s41181-017-0029-5L-nordeprenyl-D2Organic precursor[11C]L-deprenyl-D2Automated synthesisPET radiopharmaceutical |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kevin Zirbesegger Pablo Buccino Ingrid Kreimerman Henry Engler Williams Porcal Eduardo Savio |
spellingShingle |
Kevin Zirbesegger Pablo Buccino Ingrid Kreimerman Henry Engler Williams Porcal Eduardo Savio An efficient preparation of labelling precursor of [11C]L-deprenyl-D2 and automated radiosynthesis EJNMMI Radiopharmacy and Chemistry L-nordeprenyl-D2 Organic precursor [11C]L-deprenyl-D2 Automated synthesis PET radiopharmaceutical |
author_facet |
Kevin Zirbesegger Pablo Buccino Ingrid Kreimerman Henry Engler Williams Porcal Eduardo Savio |
author_sort |
Kevin Zirbesegger |
title |
An efficient preparation of labelling precursor of [11C]L-deprenyl-D2 and automated radiosynthesis |
title_short |
An efficient preparation of labelling precursor of [11C]L-deprenyl-D2 and automated radiosynthesis |
title_full |
An efficient preparation of labelling precursor of [11C]L-deprenyl-D2 and automated radiosynthesis |
title_fullStr |
An efficient preparation of labelling precursor of [11C]L-deprenyl-D2 and automated radiosynthesis |
title_full_unstemmed |
An efficient preparation of labelling precursor of [11C]L-deprenyl-D2 and automated radiosynthesis |
title_sort |
efficient preparation of labelling precursor of [11c]l-deprenyl-d2 and automated radiosynthesis |
publisher |
SpringerOpen |
series |
EJNMMI Radiopharmacy and Chemistry |
issn |
2365-421X |
publishDate |
2017-07-01 |
description |
Abstract Background The synthesis of [11C]L-deprenyl-D2 for imaging of astrocytosis with positron emission tomography (PET) in neurodegenerative diseases has been previously reported. [11C]L-deprenyl-D2 radiosynthesis requires a precursor, L-nordeprenyl-D2, which has been previously synthesized from L-amphetamine as starting material with low overall yields. Here, we present an efficient synthesis of L-nordeprenyl-D2 organic precursor as free base and automated radiosynthesis of [11C]L-deprenyl-D2 for PET imaging of astrocytosis. The L-nordeprenyl-D2 precursor was synthesized from the easily commercial available and cheap reagent L-phenylalanine in five steps. Next, N-alkylation of L-nordeprenyl-D2 free base with [11C]MeOTf was optimized using the automated commercial platform GE TRACERlab® FX C Pro. Results A simple and efficient synthesis of L-nordeprenyl-D2 precursor of [11C]L-deprenyl-D2 as free base has been developed in five synthetic steps with an overall yield of 33%. The precursor as free base has been stable for 9 months stored at low temperature (−20 °C). The labelled product was obtained with 44 ± 13% (n = 12) (end of synthesis, decay corrected) radiochemical yield from [11C]MeI after 35 min synthesis time. The radiochemical purity was over 99% in all cases and specific activity was (170 ± 116) GBq/μmol. Conclusions A high-yield synthesis of [11C]L-deprenyl-D2 has been achieved with high purity and specific activity. L-nordeprenyl-D2 precursor as free amine was applicable for automated production in a commercial synthesis module for preclinical and clinical application. |
topic |
L-nordeprenyl-D2 Organic precursor [11C]L-deprenyl-D2 Automated synthesis PET radiopharmaceutical |
url |
http://link.springer.com/article/10.1186/s41181-017-0029-5 |
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