Abstract
A reversed-phase liquid chromatographic method (RP-LC) is proposed and validated for the analysis of branched-chain amino acids (
l-leucine,
l-isoleucine and
l-valine) in new pharmaceutical formulations. The pre-column derivatization reaction of these amino acids with 2,4-dinitrofluorobenzene (DNFB) has been investigated considering the matrix effect. The compound reacts at 60
°C for 10
min at pH 9 with the amino function, in presence of cetyltrimethylammonium bromide (CTAB), to give adducts that have been separated on a RP amide C16 column and detected at
λ
=
360
nm. Linear responses were observed for each derivative. The intra-day precision (R.S.D.) was ≤2.22% and there was no significant difference between intra- and inter-day data. Recovery studies showed good results for all amino acids (98.9–100.9%) with R.S.D. ranging from 0.1% to 0.8%. The limit of quantitation was about 20
nmol/mL.