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Vol. 29, Issue 12, 1588-1598, December 2001
College of Pharmacy, Division of Pharmaceutics (C.R.G., A.E.S.),
Division of Medicinal Chemistry (W.T., A.H.S.), Department of Pathology
(R.F.B., W.Y.), and Campus Chemical Instrumentation Center Mass
Spectrometry Facility (K.G.C., N.M.K., R.B.J.), The Ohio State
University, Columbus, Ohio
Boron neutron capture therapy (BNCT) is based on a nuclear capture
reaction that occurs when boron-10, a stable isotope, is irradiated
with low energy neutrons to produce high-energy alpha particles and
recoiling lithium-7 nuclei. The purpose of the present study was to
determine what urinary metabolites, if any, could be detected in
patients with brain tumors who were given sodium borocaptate (BSH), a
drug that has been used clinically for BNCT. BSH was infused
intravenously over a 1-h time period at doses of 26.5, 44.1, or 88.2 mg/kg of body weight to patients with high-grade brain tumors.
Electrospray ionization mass spectrometry has been used to investigate
possible urinary metabolites of BSH. Chemical and instrument conditions
were established to detect BSH and its possible metabolites in both
positive and negative electrospray ionization modes. Using this
methodology, boronated ions were found in patients' urine samples that
appeared to be consistent with the following chemical structures: BSH
sulfenic acid (BSOH), BSH sulfinic acid (BSO2H), BSH
disulfide (BSSB), BSH thiosulfinate (BSOSB), and a
BSH-S-cysteine conjugate (BSH-CYS). Although BSH has
been used clinically for BNCT since the late 1960s, this is the first
report of specific biotransformation products following administration
to patients. Further studies will be required to determine both the
biological significance of these metabolites and whether any of these
accumulate in significant amounts in brain tumors.