N. Ratnaraj et Pn. Patsalos, A HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY MICROMETHOD FOR THE SIMULTANEOUS DETERMINATION OF VIGABATRIN AND GABAPENTIN IN SERUM, Therapeutic drug monitoring, 20(4), 1998, pp. 430-434
A gradient high-performance liquid chromatography micromethod is descr
ibed for the simultaneous quantitation of vigabatrin and gabapentin in
human serum. Chromatography was performed using a 125- x 3-mm ID Hype
rsil BDS C-18 column with a 3-mu m mini-bore, eluted with a gradient s
ystem comprised of phosphate buffer (pH 6.5)-acetonitrile-methanol-wat
er at a flow rate of 0.45 ml/minute. The column eluent was monitored o
n a fluorescence detector using excitation and emission wavelengths of
340 and 440 nm, respectively. The lower limit of quantitation for vig
abatrin and for gabapentin was 5 mu mol/l, and the within batch and be
tween-batch coefficients of variation were <5%. No interference from c
ommonly prescribed antiepileptic drugs (carbamazepine and its metaboli
te carbamazepine epoxide, oxcarbazepine and its metabolite 10-hydroxyi
carbazepine, ethosuximide, lamotrigine, phenobarbitone, phenytoin, pri
midone, and valproic acid) was observed; thus, the method can be used
to monitor vigabatrin and gabapentin in patients on polytherapy antiep
ileptic drug regimens.