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University of California at Davis, Davis, California
Correspondence: For reprints contact: Neal Peek, Crocker Nuclear Laboratory, University of California, Davis, Calif. 95616.
ABSTRACT
A cyclotron procedure for the production of high-purity, carrier-free 123I suitable for immediate radio-pharmaceutical use has been developed. Proton irradiation of natural elemental iodine results in the production of 123Xe which subsequently decays to 123I. The primary reaction for 57-MeV protons is 127I(p,5n)123Xe; other reactions yield 125Xe and the neutron-deficient radioisotopes of iodine. At the end of bombardment, the target iodine is dissolved in aqueous KI, and helium gas is bubbled through the solution, sweeping the xenon through a recirculating system. The xenon gas is collected in a liquid nitrogen-cooled trap. The isolated xenon is contained for 6 hr during which time the 123Xe (T1/2, 2.1 hr) decays to 123I. The 123I may be recovered by adding a small volume of physiological saline.
An irradiation on the Crocker Nuclear Laboratory isochronous cyclotron of 1 hr, using a 1 gm/cm2 thickness of iodine (7-MeV proton energy loss in the target) and 57.5-MeV protons at 6 µA, resulted in 24 isolable mCi of 123I. The only detectable contaminant in the final product was 125I which was about 0.1% of the 123I activity.
A reasonable extrapolation of our irradiation experience indicates that a yield of 89 mCi can be obtained in practice. This production figure is based on a target thickness of 1 gm/cm2 and an irradiation time of 3 hr at 10 µA.
The advantages of this method over existing methods are (A) readily available, inexpensive, isotopically pure targets; (B) multimillicurie yields of carrier-free 123I, and (C) significantly reduced radio-nuclidic contamination. When used in vivo the radiation dose to the patient is reduced and optimal spatial resolution is possible for imaging procedures. This method, however, requires 5060-MeV protons which are not universally available.
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