Data Entry: Please note that the research database will be replaced by UNIverse by the end of October 2023. Please enter your data into the system https://universe-intern.unibas.ch. Thanks

Login for users with Unibas email account...

Login for registered users without Unibas email account...

 
68Ga-PET: a powerful generator-based alternative to cyclotron-based PET radiopharmaceuticals
JournalItem (Reviews, Editorials, Rezensionen, Urteilsanmerkungen etc. in einer wissenschaftlichen Zeitschrift)
 
ID 1197302
Author(s) Fani, Melpomeni; André, João P; Maecke, Helmut R
Author(s) at UniBasel Mäcke, Helmut
Year 2008
Title 68Ga-PET: a powerful generator-based alternative to cyclotron-based PET radiopharmaceuticals
Journal Contrast media & molecular imaging
Volume 3
Number 2
Pages 67-77
Abstract PET (positron emission tomography) is a powerful diagnostic and imaging technique which requires short-lived positron emitting isotopes. The most commonly used are accelerator-produced (11)C and (18)F. An alternative is the use of metallic positron emitters. Among them (68)Ga deserves special attention because of its availability from long-lived (68)Ge/(68)Ga generator systems which render (68)Ga radiopharmacy independent of an onsite cyclotron. The coordination chemistry of Ga(3+) is dominated by its hard acid character. A variety of mono- and bifunctional chelators have been developed which allow the formation of stable (68)Ga(3+)complexes and convenient coupling to biomolecules. (68)Ga coupling to small biomolecules is potentially an alternative to (18)F- and (11)C-based radiopharmacy. In particular, peptides targeting G-protein coupled receptors overexpressed on human tumour cells have shown preclinically and clinically high and specific tumour uptake. Kit-formulated precursors along with the generator may be provided, similar to the (99)Mo/(99m)Tc-based radiopharmacy, still the mainstay of nuclear medicine.
Publisher Wiley
ISSN/ISBN 1555-4309
edoc-URL http://edoc.unibas.ch/dok/A6007457
Full Text on edoc No
Digital Object Identifier DOI 10.1002/cmmi.232
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/18383558
Document type (ISI) Journal Article, Review
 
   

MCSS v5.8 PRO. 0.342 sec, queries - 0.000 sec ©Universität Basel  |  Impressum   |    
26/04/2024