ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR SIMULTANEOUS ESTIMATION OF AMBROXOL AND DESLORATADINE IN ITS PHARMACEUTICAL DOSAGE FORM BY RP-HPLC
*Prince Francis Moses, Prathap Singh, Alagar Raja, David Banji
ABSTRACT
The present manuscript describes a new simple, specific and accurate
reverse phase high performance liquid chromatographic method for the
simultaneous determination of ambroxol and desloratadine in its tablet
dosage forms. The estimation was carried out by using Inertsil C18(4.6
× 250 mm, 5 um) column with mobile phase containing Acetonitrile:
Ammonium acetate buffer in the ratio of 40: 60 (v/v, 0.2ml of
Triethylamine) and the buffer pH was maintained at 3.5 and adjusted
with 0.01M glacial acetic acid, which is pumped at a flow rate of 1.0
ml/min.The Injection volume is 20μl and detection was monitored at
252 nm. The peaks obtained were sharp with retention times of
ambroxol and desloratadine were 4.35 min and 6.132 min,
respectively. The linearity for ambroxol was in the range of 18.75-
112.5μg/ml, and desloratadine shows linearity in the range of 1.25-
7.5μg/ml respectively. The % recoveries of ambroxol and desloratadine were found to be in
the range of 99.57% and 99.7% respectively. The proposed method was validated and
successfully applied to the estimation of ambroxol and desloratadine in combined tablet
dosage forms
Keywords: Ambroxol, desloratadine, simultaneous estimation, RP-HPLC.
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