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Drug Test Anal ; 2(3): 130-6, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20878894

ABSTRACT

The stability of tazarotene (TZ) was investigated and two stability-indicating methods-namely, first derivative and a derivative ratio spectrophotometric method-were used to determine tazarotene in the presence of its alkaline degradation product (HD) using methanol as a solvent. A linear relationship was obtained in the range 1-10 µg ml⁻¹ for both methods. By applying the proposed methods, it was possible to determine tazarotene in its pure powdered from with accuracy 99.35 ± 1.410 (n = 10) for the first derivative method and 99.45 ± 1.053 (n = 10) for the derivative ratio method. First derivative and derivative ratio methods were used for the analysis of laboratory-prepared mixtures containing different ratios of tazarotene and its degradation product and they were valid in the presence of up to 70% and 80% degradation product, respectively. The proposed methods were validated and found to be suitable as stability-indicating assay methods for tazarotene in pharmaceutical formulations.


Subject(s)
Hydroxides/chemistry , Nicotinic Acids/analysis , Potassium Compounds/chemistry , Calibration , Drug Stability , Hydrolysis , Mass Spectrometry , Molecular Structure , Nicotinic Acids/chemistry , Reproducibility of Results , Spectrophotometry, Infrared , Spectrophotometry, Ultraviolet/methods
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