Forced Degradation Behaviour of Fluphenazine Hydrochloride by LC and Characterization of its Oxidative Degradation Product by LC-MS/MS.

Autor: Thummar KN; Department of Pharmaceutical Sciences, Saurashtra University, Rajkot - 360005, Gujarat, India., Ghava DJ; Department of Pharmaceutical Sciences, Saurashtra University, Rajkot - 360005, Gujarat, India., Mistry A; Department of Pharmaceutical Sciences, Saurashtra University, Rajkot - 360005, Gujarat, India., Vachhani A; Department of Pharmaceutical Sciences, Saurashtra University, Rajkot - 360005, Gujarat, India., Sheth NR; Department of Pharmaceutical Sciences, Saurashtra University, Rajkot - 360005, Gujarat, India.
Jazyk: angličtina
Zdroj: Scientia pharmaceutica [Sci Pharm] 2014 Dec 22; Vol. 83 (2), pp. 297-309. Date of Electronic Publication: 2014 Dec 22 (Print Publication: 2015).
DOI: 10.3797/scipharm.1411-04
Abstrakt: A novel, stability-indicating high-performance liquid chromatographic (HPLC) method is delivered for the determination of fluphenazine hydrochloride (FPZ) and its degradation products. The forced degradation testing of FPZ was carried out for hydrolytic, oxidative, photolytic, and thermal degradation. The degradation appeared using a reversed-phase C18 column at ambient temperature with a mobile phase comprised of methanol : acetonitrile : (10 mM) ammonium acetate (70:15:15, v/v/v) pH 6.0, adjusted with acetic acid, having a flow rate of 1 ml min(-1) and a detection wavelength at 259 nm. Primarily, the maximum degradation products were formed under oxidative stress conditions. The product was distinguished through LC-MS/MS fragmentation studies. Based on the results, a more complete degradation pathway for the drug could be proposed. The modernized method was found to be precise, accurate, specific, and selective. The method was found to be suitable for the quality control of fluphenazine hydrochloride in the tablet as well as in stability-indicating studies.
Databáze: MEDLINE