A liquid chromatographic procedure for the direct determination of tin
idazole in human serum is presented, It includes the use of a micellar
mobile phase consisting of SDS (5.10(-2) ha): propan-1-ol; (94:6; v/v
) and a mu Bondapak CN column with UV detection at 320 nm, No solvent
extraction or deproteinization are necessary, The linearity (0.1-10 mg
L), the precision (3%), the reproducibility (1.3%), the recovery (99%
), and the detection limit (0.1 mg L) in the tinidazole determination
are comparable and sometimes greater than the corresponding tinidazole
parameters when deproteinization and conventional reversed-phase HPLC
are used, One hundred injections of serum samples do not affect the c
olumn life, The procedure is applied to ascertain the pharmacokinetics
of 10 mg/kg of tinidazole.