Tracers / [18F]FE-PE2I

[18F]FE-PE2I

Also written as [18F]FE-PE2I; [F-18]FE-PE2I; FE-PE2I
Radionuclide
F-18 t½ 109.77 min
Modality
PET
Production route
Stage
Syntheses indexed
5

What it is

Compound class
Cocaine derivative / tropane-based dopamine transporter (DAT) ligand
Target / mechanism
Dopamine transporter (DAT) PMID 38696063
Clinical application
PET imaging of dopamine transporter density for diagnosis of Parkinson's disease PMID 34206688
Theranostic pair

Regulatory status

FDA
EMA (centralised)
Other approvals
Brand names

Clinical use

Typical injected activity
Uptake time

Reported in the literature. Not a dosing recommendation.

Published syntheses

ModuleCassettePurificationYield %RCP %Precursor / supplierSource
ScanSys synthesizer
Scansys Laboratorieteknik
fixed tubingHPLC7.6 ± 3.6%OTsE-PE2I (tosylethyl-PE2I)
PharmaSynth AS, Tartu, Estonia
34206688
2021 Pharmaceuticals (Basel)
an automated radiochemistry system (Scansys Laboratorieteknik ApS) with a preparative Onyx C18 high-performance liquid chromatography (HPLC) system — reasonable RCYs of 7.6 ± 3.6% (n = 73, starting from ca. 45 GBq as the standard) were achieved
ScanSys synthesizer
Scansys Laboratorieteknik
fixed tubingHPLC10.8 ± 3.7%OTsE-PE2I (tosylethyl-PE2I)
PharmaSynth AS, Tartu, Estonia
34206688
2021 Pharmaceuticals (Basel)
Applying the improved preparative HPLC conditions with the ascorbate buffer improved the RCYs slightly (10.8 ± 3.7%, n = 161). — Applying the improved preparative HPLC conditions with the ascorbate buffer improved the RCYs slightly (10.8 ± 3.7%, n = 161).
Synthera+
IBA
vendor cassetteHPLC16.9 ± 2.7%OTsE-PE2I / TsOE-PE2I
PharmaSynth AS, Tartu, Estonia
34206688
2021 Pharmaceuticals (Basel)
the production of [18F]FE-PE2I was transferred to a cassette-based system using a Synthera®+ HPLC (IBA). — The process was fully validated with starting activities up to 140 GBq giving an average RCY of 16.9 ± 2.7% (n = 3).
Synthera+
IBA
vendor cassetteHPLC33 ± 2%OTsE-PE2I / TsOE-PE2I
PharmaSynth AS, Tartu, Estonia
34206688
2021 Pharmaceuticals (Basel)
The synthesis was implemented on the Synthera®+ module — Using DMSO as the reaction solvent generated the product with the RCY of 33 ± 2% (n = 3) from the 45-GBq starting activity (Figure 8).
TRACERlab FX2 N
GE HealthCare
custom manifoldHPLC+SPE39 ± 8%
yes
>95%tosylethyl-PE2I
PharmaSynth AS, Tartu, Estonia
38696063
2024 EJNMMI Radiopharm Chem
GE TRACERLab FX2 N — [18F]FE-PE2I was produced with a radiochemical yield of 39 ± 8% (n = 4, relative [18F]F− delivered to the module)

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Quality control Preliminary — inferred from compound class

Ph. Eur. monograph
USP monograph
AppearancepHRCP HPLCRCP TLCHPLC UVRadionuclidic (HPGe)Half-lifeActivityEndotoxins (LAL)SterilityFilter integrity
How this set was arrived at. base set per Ph. Eur. general monograph 0125 (rule); organic-phase radiosynthesis assumed from isotope/compound class, no synthesis data confirming it -> GC residual solvents (preliminary); conventional nucleophilic 18F-fluorination assumed from isotope/compound class, no synthesis data confirming K222 use -> Kryptofix test (preliminary)

Tests listed by reference only. Monograph texts are copyrighted and are not reproduced here. How these are derived

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Notes

Added from reverse module search (stage 6); 2 article(s) with F-18.