Ricerca avanzata

Home > Riviste > The Quarterly Journal of Nuclear Medicine and Molecular Imaging > Fascicoli precedenti > The Quarterly Journal of Nuclear Medicine and Molecular Imaging 2009 Agosto;53(4) > The Quarterly Journal of Nuclear Medicine and Molecular Imaging 2009 Agosto;53(4):411-6

FASCICOLI E ARTICOLI   I PIÙ LETTI   eTOC

ULTIMO FASCICOLOTHE QUARTERLY JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING

Rivista di Medicina Nucleare e Imaging Molecolare

A Journal on Nuclear Medicine and Molecular Imaging
Affiliated to the Society of Radiopharmaceutical Sciences and to the International Research Group of Immunoscintigraphy
Indexed/Abstracted in: Current Contents/Clinical Medicine, EMBASE, PubMed/MEDLINE, Science Citation Index (SciSearch), Scopus
Impact Factor 2,413

Periodicità: Trimestrale

ISSN 1824-4785

Online ISSN 1827-1936

 

The Quarterly Journal of Nuclear Medicine and Molecular Imaging 2009 Agosto;53(4):411-6

LATEST ADVANCES IN RADIOPHARMACOLOGY AND RADIOPHARMACY 2009 

 REVIEWS

Fast high performance liquid chromatography in PET quality control and metabolite analysis

Passchier J.

GlaxoSmithkline, Clinical Imaging Center, Imperial College, Hammersmith Hospital, London, UK

Quality control (QC) and metabolite analysis on compounds labelled with positron emitting isotopes used for positron emission tomography (PET) studies are constrained by time. For carbon-11 labelled tracers, it is generally accepted that the QC and subsequent release process should take no longer than 20 minutes to ensure both high product specific activity and activity in order to meet the aims of the studies in which it is used. From a regulatory point of view, PET manufacturing and associated QC testing are increasingly expected to meet Good Manufacturing Practices (GMP) standards. The challenge for the PET QC laboratory of today is to marry the requirement for fast testing with meeting applicable regulations and guidance. Although regulatory requirements are typically less of an issue for PET metabolite analysis, it has a significant impact on the ability to perform quantitative PET pharmacokinetic analysis on the acquired PET imaging data. This paper aims to provide a general overview and guidance on good practice for PET HPLC quality control and aims to highlight some recent developments that may aid in speeding up both PET QC and metabolite HPLC analysis methods.

lingua: Inglese


FULL TEXT  ESTRATTI

inizio pagina