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Vol. 31, Issue 1, 114-121, January 2003
Faculties of Pharmaceutical Sciences (V.S.G., W.T., F.S.A.) and
Medicine (K.F.), University of British Columbia, Vancouver, Canada
In this study, spectroscopic and chromatographic evidence is
presented for the identification and characterization of the metabolites, valproyl glutamate (2-propylpentanoyl glutamate, VPA-GLU)
and valproyl glutamine (2-propylpentanoyl glutamine, VPA-GLN) in the
urine, serum, and cerebrospinal fluid (CSF) of patients on
valproic acid (VPA) therapy. Moreover, the identification of
valproyl glycine (2-propylpentanoyl glycine, VPA-GLY) in the serum and
urine of patients on VPA, albeit in trace concentrations, is also
reported here. The three amino acid conjugates excreted in urine
accounted for about 1% of the VPA dose in four patients who were on
VPA therapy chronically and had reached steady state. VPA-GLU was
quantitatively the most prominent metabolite (0.66-13.1 µg/mg
creatinine) compared with VPA-GLN (0.78-9.93 µg/mg creatinine) and
VPA-GLY (trace-1.0 µg/mg creatinine) in overnight urine samples of
all patients studied (n = 29). The relatively low
serum concentrations of the three amino acid conjugates of VPA in six
patients suggest that the metabolites are readily excreted once formed.
In contrast, whereas VPA GLY was absent in the CSF of one patient on
VPA, the concentrations of VPA-GLU and VPA-GLN in this CSF sample were 9 and 5 times, respectively, their corresponding serum concentrations.
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