The Role of Dynamic Positron Emission Tomography for Quantifying Boron-10 in Vivo Using the Fructose Complex of Fluorine-18 Labeled Boronophenylalanine

  • G. W. Kabalka
  • G. T. Smith
  • T. L. Nichols
  • J. P. Dyke
  • D. Longford
  • K. F. Hubner

Abstract

One of the major difficulties facing successful boron neutron capture therapy (BNCT) is the paucity of in vivo pharmacokinetic data.1 Analytical techniques such as prompt gamma analysis, secondary ion mass spectrometry, and resonance ionization spectroscopy are simply not applicable to the in vivo detection of boron.2 To address this problem, both positron emission tomography (PET)3,4 and magnetic resonance imaging (MRI)5 techniques for the in vivo detection of boronated compounds are being developed. Nuclear medicine diagnostic techniques such as PET have proven to be extremely valuable in evaluating a variety of physiological parameters including the pharmacokinetic behavior of therapeutic agents.6,7,8 In fact, over nine thousand patients have been evaluated at The University of Tennessee utilizing PET since 1989.

Keywords

Arthritis Boron Sarcoma Resid Fructose 

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Copyright information

© Springer Science+Business Media New York 2001

Authors and Affiliations

  • G. W. Kabalka
    • 1
  • G. T. Smith
    • 1
  • T. L. Nichols
    • 1
  • J. P. Dyke
    • 1
  • D. Longford
    • 1
  • K. F. Hubner
    • 1
  1. 1.Biomedical Imaging CenterThe University of Tennessee Medical CenterKnoxvilleUSA

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