Pb. Shetkar et Vm. Shinde, SIMULTANEUOUS DETERMINATION OF ENALPRIL MALEATE AND HYDROCHLOROTHIAZIDE IN TABLETS BY REVERSED-PHASE HPLC, Analytical letters, 30(6), 1997, pp. 1143-1152
A new simple, precise, rapid and selective RP-HPLC method has been dev
eloped for the simultaneous determination of Enalpril maleate and Hydr
ochlorothiazide from formulations, using 0.025M orthophosphoric acid [
(adjusted to pH 3.0 with triethyl amine (TEA)]: Acetonitrile (84 16 V/
V), as a mobile phase at a flow rate of 1.0 ml/min and mu Bondapak C-1
8 column (10 micron, 30cm x 3.9 mm) as a stationary phase. Detection w
as carried out using a UV detector at 226 nm. p-hydroxy phenyl acetami
de (PHPA) was used as an internal standard. Linearity range and percen
tage recoveries for Enalpril maleate and Hydrochlorothiazide were 40-2
00 mu g/ml and 50-500 mu g/ml, 99.74 and 99.69 respectively. Minimum d
etection limit obtained was 0.8 mu g/ml and 0.4 mu/ml for Enalpril mal
eate and Hydrochlorothiazide respectively.