THERAPEUTIC EFFICACY OF HYDROCHLOROTHIAZIDE WITH LOSARTAN AS A FIXED DOSE COMBINATION BY LC-MS/MS

Abstract

The main aim of the present research work is to evaluate the pharmacokinetic parameters as well as therapeutic efficacy of Hydrochlorothiazide along
with Losartan used as a fixed dose combined drug in treatment of hypertension. This study is carried out by utilizing a typical two periods; randomized
and two way complete cross over design. All the 6 volunteers are received fixed dose and single dose product based on the randomization code in each
clinical period. Then blood samples are taken and the comparative Pharmacokinetic study was carried out. Matrix effect for internal standard (Letrozole
and Candesartan) and analytes (Losartan, LCA & HTCZ) were also carried out as per US-FDA guideline. Maximum plasma concentration of fixed dose
combining drug (in which Losartan combined with HCTZ) was found 49 ± 8.87 ng/ml (Cmax) at time 2.75 ± 0.25 hours (tmax) for HCTZ and the average
maximum plasma concentration of 6 volunteers was 49.87 ng/ml and Tmax 2.75 hours, AUC0-t was 227.02 ng/ml at 48 hours and AUC0-α227.67 ng/ml
at infinite time and plasma half-life (T1/2) of HCTZ 4.91 hours and Ket value is 0.14 hour-1. The matrix effect of internal standard (letrozole) ranged
between 87.32% - 89.71% and for HCTZ it was between 88.47% - 89.86%. And the matrix effect of internal standard (Candesartan) ranged between
93.77% - 98.28% and same was found between 95.97% - 96.78% in case of Losartan and for LCA it was 95.41% - 98.39%. From the comparative
pharmacokinetic study it can be concluded that after fixed dose combined drug treatment the maximum plasma concentration of losartan and losartan
carboxylic acid were too much higher than the maximum concentration of losartan and LCA after single drug containing losartan only. And fixed dose
combination drug is more susceptible than single dose of Losartan for the treatment of hypertension with better therapeutic efficacy.