Advancing 6-bromo-7-[11C]methylpurine to clinical use: improved regioselective radiosynthesis, non-clinical toxicity data and human dosimetry estimates
Status PubMed-not-MEDLINE Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
882717
Österreichische Forschungsförderungsgesellschaft
327571
Norwegian Research Council (NFR)
8F21002
Ministry of Education, Youth and Sports (MŠMT)
PubMed
38683266
PubMed Central
PMC11058743
DOI
10.1186/s41181-024-00265-z
PII: 10.1186/s41181-024-00265-z
Knihovny.cz E-zdroje
- Klíčová slova
- 6-Bromo-7-[11C]methylpurine, Investigational medicinal product dossier, Multidrug resistance-associated protein 1, PET, Regioselective N‑alkylation,
- Publikační typ
- časopisecké články MeSH
BACKGROUND: 6-Bromo-7-[11C]methylpurine ([11C]BMP) is a radiotracer for positron emission tomography (PET) to measure multidrug resistance-associated protein 1 (MRP1) transport activity in different tissues. Previously reported radiosyntheses of [11C]BMP afforded a mixture of 7- and 9-[11C]methyl regioisomers. To prepare for clinical use, we here report an improved regioselective radiosynthesis of [11C]BMP, the results of a non-clinical toxicity study as well as human dosimetry estimates based on mouse PET data. RESULTS: [11C]BMP was synthesised by regioselective N7-methylation of 6-bromo-7H-purine (prepared under good manufacturing practice) with [11C]methyl triflate in presence of 2,2,6,6-tetramethylpiperidine magnesium chloride in a TRACERlab™ FX2 C synthesis module. [11C]BMP was obtained within a total synthesis time of approximately 43 min in a decay-corrected radiochemical yield of 20.5 ± 5.2%, based on starting [11C]methyl iodide, with a radiochemical purity > 99% and a molar activity at end of synthesis of 197 ± 130 GBq/μmol (n = 28). An extended single-dose toxicity study conducted in male and female Wistar rats under good laboratory practice after single intravenous (i.v.) administration of unlabelled BMP (2 mg/kg body weight) revealed no test item related adverse effects. Human dosimetry estimates, based on dynamic whole-body PET data in female C57BL/6J mice, suggested that an i.v. injected activity amount of 400 MBq of [11C]BMP will deliver an effective dose in the typical range of 11C-labelled radiotracers. CONCLUSIONS: [11C]BMP can be produced in sufficient amounts and acceptable quality for clinical use. Data from the non-clinical safety evaluation showed no adverse effects and suggested that the administration of [11C]BMP will be safe and well tolerated in humans.
Biomedical Research Center University Hospital Hradec Kralove Hradec Kralove Czech Republic
Department Computer Science University of Applied Sciences Technikum Wien Vienna Austria
Department of Clinical Pharmacology Medical University of Vienna Vienna Austria
Department of Nuclear Medicine Medical University Innsbruck Innsbruck Austria
Department of Pharmacology Faculty of Medicine University of Latvia Rīga Latvia
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