Your browser doesn't support javascript.
loading
GMP production of [18F]FE-PE2I on a TRACERLab FX2 N synthesis module, a radiotracer for in vivo PET imaging of the dopamine transport.
Ferrat, Mélodie; Moein, Mohammad M; Cananau, Carmen; Tegnebratt, Tetyana; Saliba, Paul; Norman, Fredrik; Steiger, Carsten; Bratteby, Klas; Samén, Erik; Dahl, Kenneth; Tran, Thuy A.
Afiliación
  • Ferrat M; Department of Radiopharmacy, Karolinska University Hospital, 171 76, Stockholm, Sweden. melodie.ferrat@ki.se.
  • Moein MM; Department of Oncology and Pathology, Karolinska Institutet, 171 76, Stockholm, Sweden. melodie.ferrat@ki.se.
  • Cananau C; Department of Radiopharmacy, Karolinska University Hospital, 171 76, Stockholm, Sweden.
  • Tegnebratt T; Department of Oncology and Pathology, Karolinska Institutet, 171 76, Stockholm, Sweden.
  • Saliba P; Department of Medical Radiation Physics and Nuclear Medicine, Karolinska University Hospital, 171 76, Stockholm, Sweden.
  • Norman F; Department of Radiopharmacy, Karolinska University Hospital, 171 76, Stockholm, Sweden.
  • Steiger C; Department of Radiopharmacy, Karolinska University Hospital, 171 76, Stockholm, Sweden.
  • Bratteby K; Department of Radiopharmacy, Karolinska University Hospital, 171 76, Stockholm, Sweden.
  • Samén E; Department of Radiopharmacy, Karolinska University Hospital, 171 76, Stockholm, Sweden.
  • Dahl K; Department of Radiopharmacy, Karolinska University Hospital, 171 76, Stockholm, Sweden.
  • Tran TA; Department of Oncology and Pathology, Karolinska Institutet, 171 76, Stockholm, Sweden.
EJNMMI Radiopharm Chem ; 9(1): 35, 2024 May 02.
Article en En | MEDLINE | ID: mdl-38696063
ABSTRACT

BACKGROUND:

Parkinson's disease is a neurodegenerative disorder that is characterized by a degeneration of the dopaminergic system. Dopamine transporter (DAT) positron emission tomography (PET) imaging has emerged as a powerful and non-invasive method to quantify dopaminergic function in the living brain. The PET radioligand, [18F]FE-PE2I, a cocaine chemical derivative, has shown promising properties for in vivo PET imaging of DAT, including high affinity and selectivity for DAT, excellent brain permeability, and favorable metabolism. The aim of the current study was to scale up the production of [18F]FE-PE2I to fulfil the increasing clinical demand for this tracer.

RESULTS:

Thus, a fully automated and GMP-compliant production procedure has been developed using a commercially available radiosynthesis module 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). The synthesis time was 70 min, and the molar activity was 925.3 ± 763 GBq/µmol (250 ± 20 Ci/µmol). The produced [18F]FE-PE2I was stable over 6 h at room temperature.

CONCLUSION:

The protocol reliably provides a sterile and pyrogen-free GMP-compliant product.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: EJNMMI Radiopharm Chem Año: 2024 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: EJNMMI Radiopharm Chem Año: 2024 Tipo del documento: Article País de afiliación: Suecia