Holmium-166 (Ho-166, t(1/2) = 26.4 h) is utilized in radiotherapeutic
applications such as radioimmunospecific pharmaceuticals, bone marrow
ablation, and radiation synovectomy. High specific activity Ho-166 can
be obtained from the decay of dysprosium-166 (Dy-166, t(1/2) = 81.5 h
). Dysprosium-166 is produced by the Dy-164[n,gamma]Dy-165[n,gamma]Dy-
166 reaction in a nuclear reactor. The applicability of reversed phase
ion-exchange chromatographic methods was demonstrated for the separat
ion of carrier-free Ho-166 from milligram quantities of (Dy2O3)-Dy-164
irradiated targets. An efficient and quantitative separation was achi
eved utilizing a metal-free HPLC system with Dowex AG 50WX12 or Aminex
-A5 cation exchangers and alpha-hydroxyisobutyric acid (alpha-MIBA) as
the eluent (0.085 M, pH 4.3 adjusted with NH4OH). The Aminex-A5 colum
n gave a separation factor of similar to 10(3) between Ho and Dy. Subs
equent to the acidic destruction of the Ho-HIBA complex, Ho3+ was furt
her purified on a small cation-exchange column from acidic chloride so
lutions. The separation was achieved within 2 h, with a 95% overall ra
diochemical yield for carrier-free Ho-166 with a DY breakthrough of <0
.1%.