Startseite Radiochemical separation of no-carrier-added radioniobium from zirconiu targets for application of 90Nb-labelled compounds
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Radiochemical separation of no-carrier-added radioniobium from zirconiu targets for application of 90Nb-labelled compounds

  • S. Busse , J. Brockmann und Frank Rösch
Veröffentlicht/Copyright: 25. September 2009

Summary

The radioisotope 90Nb is a positron emitter with a relatively high positron branching of 51% and a rather low β+-energy of Emean = 662 keV Emax = 1.5 MeV) with potential for application in positron emission tomography (PET). Its half-life of 14.6 h makes it especially promising for the quantitative investigation of biological processes with slow distribution kinetics. An advantageous production route of 90Nb is the natZr(p, n)90Nb process. To separate nca (no-carrier-added) radioniobium from macroscopic amounts of irradiated zirconium targets, an effective two step separation procedure was developed. A liquid-liquid extraction using N-benzoyl-N-phenylhydroxylamine (BPHA) in CHCl3 was applied first to separate the bulk of the zirconium matrix with a Zr separation coefficient of about 104, followed by anion-exchange chromatography for high grade purification of nca radioniobium. A sufficiently high decontamination factor of > 2 × 107 and an overall radiochemical yield of nca 90Nb of about 70% was achieved within about 3 hours.

Received: 2001-10-24
Accepted: 2002-2-19
Published Online: 2009-9-25
Published in Print: 2002-7-1

© Oldenbourg Wissenschaftsverlag, München

Heruntergeladen am 10.9.2025 von https://www.degruyterbrill.com/document/doi/10.1524/ract.2002.90.7_2002.411/html
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