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Synthesis of (11)C‐labeled ubiquinone and ubiquinol via Pd(0)‐mediated rapid C‐[(11)C]methylation using [(11)C]methyl iodide and 39‐demethyl‐39‐(pinacolboryl)ubiquinone

To enable positron emission tomography (PET) imaging of the in vivo kinetics of ubiquinone and ubiquinol, which is referred to as coenzyme Q(10), their (11)C‐radiolabeled counterparts were synthesized herein. (11)C‐Labeled ubiquinone [(11)C]‐1 was realized by Pd‐mediated rapid C‐[(11)C]methylation o...

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Detalles Bibliográficos
Autores principales: Goto, Miki, Nishiyama, Akira, Yamaguchi, Takao, Watanabe, Kyosuke, Fujii, Kenji, Watanabe, Yasuyoshi, Doi, Hisashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590163/
https://www.ncbi.nlm.nih.gov/pubmed/30556149
http://dx.doi.org/10.1002/jlcr.3700
Descripción
Sumario:To enable positron emission tomography (PET) imaging of the in vivo kinetics of ubiquinone and ubiquinol, which is referred to as coenzyme Q(10), their (11)C‐radiolabeled counterparts were synthesized herein. (11)C‐Labeled ubiquinone [(11)C]‐1 was realized by Pd‐mediated rapid C‐[(11)C]methylation of [(11)C]CH(3)I with 39‐demethyl‐39‐(pinacolboryl)ubiquinone, prepared by Ru‐catalyzed olefin metathesis of unradiolabeled ubiquinone with 2‐(pinacolboryl)propene. Subsequent reduction of [(11)C]‐1 using Na(2)S(2)O(4) yielded (11)C‐labeled ubiquinol [(11)C]‐2. The synthesis time and [(11)C]CH(3)I‐based radiochemical yield of [(11)C]‐1 were within 36 minutes and up to 53%, while those of [(11)C]‐2 were within 38 minutes and up to 39%, respectively. After radiopharmaceutical formulation, the qualities of [(11)C]‐1 and [(11)C]‐2 were confirmed to be applicable for animal PET studies. The analytical values of [(11)C]‐1 and [(11)C]‐2 are as follows: radioactivity of up to 3.5 and 1.4 GBq, molar activity of 21 to 78 and 48 to 76 GBq/μmol, radiochemical purity of greater than 99% and greater than 95%, and chemical purity of greater than 99% and 77%, respectively. The concept behind this radiolabeling procedure is that unradiolabeled natural ubiquinone can be converted to (11)C‐radiolabeled ubiquinone and ubiquinol via a pinacolborane‐substituted ubiquinone derivative. Each PET probe was used for molecular imaging using rats to investigate the in vivo kinetics and biodistribution of the coenzyme Q(10).