A selective and sensitive method is presented for the determination of L-im
inoethyl-L-lysine (L-NIL) in rat serum. L-NIL is a selective inhibitor of t
he inducible nitric oxide synthase. The analytical technique is based upon
a two-buffer reversed-phase HPLC system with fluorescence detection of pre-
column derivatized amino acid analogue with o-phtaldialdehyde. The retentio
n time of L-NIL was 19.4 min. The limit of quantification was 0.5 mg/l. Aft
er validation, the method was used to study the pharmacokinetic profile of
L-NIL in rats after intravenous as well as oral administration of a single
dose. (C) 2000 Elsevier Science B.V. All rights reserved.