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Pharmaceutical preparation of oxygen-15 labelled molecular oxygen and carbon monoxide gasses in a hospital setting.

Authors :
Luurtsema G
Boellaard R
Greuter HN
Rijbroek A
Takkenkamp K
de Geest FG
Buijs FL
Harry Hendrikse N
Franssen EJ
van Lingen A
Lammertsma AA
Source :
Journal of clinical pharmacy and therapeutics [J Clin Pharm Ther] 2010 Feb; Vol. 35 (1), pp. 63-9.
Publication Year :
2010

Abstract

Background: Clinical positron emission tomography (PET) requires safe and effective PET radiopharmaceuticals. Tracers used for measuring oxygen consumption and blood volume are [(15)O]O(2) and [(15)O]CO, respectively. In general, these oxygen-15 labelled tracers are produced using a cyclotron that accelerates deuterons onto a target filled with (14)N(2) containing a trace of oxygen. In recent years, cyclotrons have been developed that only are capable of accelerating protons. The purpose of this study was to validate and assess such a cyclotron for production and administration of oxygen-15 labelled gasses in an hospital setting.<br />Methods: An RDS111 cyclotron (Siemens-CTI, Knoxville, USA) was validated for bolus production of [(15)O]O(2) and [(15)O]CO gasses. In addition, equipment was developed to administer these tracers to patients.<br />Results: Both [(15)O]O(2) and [(15)O]CO gasses could be produced in sufficient amounts, whilst meeting European Pharmacopeia requirements. Although produced oxygen-15 gasses contained a minor level of (11)C contamination, in clinical studies it was possible to correct for this contamination by delayed blood counting.<br />Conclusion: An 11 MeV proton cyclotron combined with an in-house developed gas delivery system allows for the production and administration of sufficient amounts of [(15)O]-gasses for routine clinical PET studies in an hospital setting.

Details

Language :
English
ISSN :
1365-2710
Volume :
35
Issue :
1
Database :
MEDLINE
Journal :
Journal of clinical pharmacy and therapeutics
Publication Type :
Academic Journal
Accession number :
20175813
Full Text :
https://doi.org/10.1111/j.1365-2710.2009.01032.x