Souri, E., Donyayi, H., Ahmadkhaniha, R., Barazandeh Tehrani, M. (2015). A Stability Indicating HPLC Method for the Determination of Fluvoxamine in Pharmaceutical Dosage Forms. Iranian Journal of Pharmaceutical Research, 14(4), 1059-1065. doi: 10.22037/ijpr.2015.1732
Effat Souri; Hassan Donyayi; Reza Ahmadkhaniha; Maliheh Barazandeh Tehrani. "A Stability Indicating HPLC Method for the Determination of Fluvoxamine in Pharmaceutical Dosage Forms". Iranian Journal of Pharmaceutical Research, 14, 4, 2015, 1059-1065. doi: 10.22037/ijpr.2015.1732
Souri, E., Donyayi, H., Ahmadkhaniha, R., Barazandeh Tehrani, M. (2015). 'A Stability Indicating HPLC Method for the Determination of Fluvoxamine in Pharmaceutical Dosage Forms', Iranian Journal of Pharmaceutical Research, 14(4), pp. 1059-1065. doi: 10.22037/ijpr.2015.1732
Souri, E., Donyayi, H., Ahmadkhaniha, R., Barazandeh Tehrani, M. A Stability Indicating HPLC Method for the Determination of Fluvoxamine in Pharmaceutical Dosage Forms. Iranian Journal of Pharmaceutical Research, 2015; 14(4): 1059-1065. doi: 10.22037/ijpr.2015.1732
A Stability Indicating HPLC Method for the Determination of Fluvoxamine in Pharmaceutical Dosage Forms
2Dept of Medicinal Chemistry, Faculty of pharmacy, Tehran University of Medical Sciences
3Dept of Human Ecology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
4Dept of Medicinal Chemistry, Faculty of Pharmacy. Tehran University of Medical Sciences, Tehran, Iran
Abstract
Fluvoxamine maleate is a selective serotonin reuptake inhibitor, which is used for the treatment of different types of depressive disorders. In the present study, a stability indicating HPLC method was developed and validated for the determination of fluvoxamine maleate. The chromatographic separation was carried out using a Nova-Pak CN column and a mixture of K2HPO4 50 mM (pH 7.0) and acetonitrile (60: 40, v/v) as the mobile phase. Target compounds were detected using a UV detector set at 235 nm. The developed method was linear over the concentration range of 1-80 μg/ml with acceptable precision (CV values < 2.0%) and accuracy (error values < 1.6%). The degradation studies showed that fluvoxamine maleate is relatively unstable under acidic, basic and oxidative conditions and also when exposed to UV radiation. On the other hand, the bulk powder of fluvoxamine maleate was relatively stable when exposed to visible light or heat. The proposed method was successfully applied for the determination of active ingredient of fluvoxamine dosage form without any interference from tablet excipients.
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