Validated methods for determination of yohimbine hydrochloride in the presence of its degradation products

Two simple, accurate and sensitive and techniques have been developed and validated for the determination of yohimbine hydrochloride in presence of its acid, alkaline and photo-degradates as stability-indicating studies. First spectrophotometric technique was adopted for the determination of the investigated drug in presence of degradation products, by the use of derivative and derivative ratio methods, respectively, while the second technique utilized a high-performance liquid chromatography for the determination of yohimbine hydrochloride in presence of its degradation products, as stability indicatingmethod. The chromatographic separation was achieved isocratically by using a mobile phase of water and methanol in a ratio of 55:45 V/V containing 0.5% triethylamine. The analysis was carried out using C18 (4.6 · 150 mm, 5 μm) at flow rate of 1.0 ml/min and UV detection at 270 nm. All the proposed methods were validated according to the International Conference on Harmonization (ICH) guidelines and successfully applied for determination of the drug in pure form, in laboratory prepared mixtures and in pharmaceutical preparations. The obtained resultswere statistically compared to the official method of analysis for yohimbine hydrochloride and no significant differences were found.