Determination of vigabatrin in plasma by reversed-phase high-performance liquid chromatography.

Abstract:

:A method is described for the determination of vigabatrin in 50 microliters of plasma by isocratic high-performance liquid chromatography using fluorescence detection. The procedure involves protein precipitation with methanol followed by precolumn derivatisation with o-phthaldialdehyde reagent. Separation of the derivatised vigabatrin was achieved on a Microsorb C18 column using a mobile phase of 10 mM orthophosphoric acid:acetonitrile:methanol (6:3:1) at a flow rate of 2.0 ml/min. Assay time is 15 min and chromatograms show no interference from commonly coadministered anticonvulsant drugs. The total analytical error within the range of 0.85-85 micrograms/ml was found to be 7.6% with the within-replicates error of 2.76%. The minimum detection limit was 0.08 micrograms/ml and the minimum quantitation limit was 0.54 micrograms/ml.

journal_name

Ther Drug Monit

authors

Tsanaclis LM,Wicks J,Williams J,Richens A

doi

10.1097/00007691-199105000-00011

subject

Has Abstract

pub_date

1991-05-01 00:00:00

pages

251-3

issue

3

eissn

0163-4356

issn

1536-3694

journal_volume

13

pub_type

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