validating a stability indicating hplc method for kinetic study of cetirizine degradation in acidic and oxidative conditions

Authors

effat souri department of medicinal chemistry, faculty of pharmacy and pharmaceutical sciences research center, tehran university of medical sciences, tehran, iran.

ali hatami department of medicinal chemistry, faculty of pharmacy and pharmaceutical sciences research center, tehran university of medical sciences, tehran, iran.

nazanin shabani ravari department of medicinal chemistry, faculty of pharmacy and pharmaceutical sciences research center, tehran university of medical sciences, tehran, iran.

farhad alvandifar department of medicinal chemistry, faculty of pharmacy and pharmaceutical sciences research center, tehran university of medical sciences, tehran, iran.

abstract

a stability indicating high-performance liquid chromatography (hplc) method wasvalidated and used to study the degradation of cetirizine dihydrochloride in acidic and oxidativeconditions. the separation was carried out on a symmetry c18 column and a mixture of 50 mmkh2po4 and acetonitrile (60:40 v/v, ph = 3.5) was used as the mobile phase. the method waslinear over the range of 1-20 μg/ml of cetirizine dihydrochloride (r2 > 0.999) and the withindayand between-day precision values were less than 1.5%. the results showed that cetirizinedihydrochloride was unstable in 2 m hcl and 0.5% h2o2. the kinetics of the acidic degradationshowed a pseudo-first-order reaction in the temperature range of 70-90°c. in addition, thekinetics of hydrogen peroxide mediated degradation was pseudo-first-order in the temperaturerange of 50-80°c.

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Journal title:
iranian journal of pharmaceutical research

جلد ۱۲، شماره ۲، صفحات ۲۸۷-۲۹۴

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