Volume 12, Issue 4, October 2022

Stability Indicating RP-HPLC Method Development and Validation for Estimation of Safinamide in Bulk Drug and Dosage Form (Research Article)

Author(s): Gayatri R. Amrutkar*, Smita S Aher and R S Bachhav
Abstract: This research article emphasizes on this research, a novel, sensitive, convenient, clear, accurate, and robust reverse-phase high-performance liquid chromatography (RP-HPLC) method was developed and validated for the determination of safinamide in drug and tablet formulation. Separation was performed by HPLC with UV detector and Open lab EZchrome workstation program, as well as Kromasil C18 (250 mm X 4.6 mm i.d.) 5 μm. Methanol: 0.025% TFAA (45:55) was pumped at a flow rate of 1.0 mL/min and detected at 226 nm.
PAGES: 92-106  |  56 VIEWS  104 DOWNLOADS

How To Cite this Article:

Gayatri R. Amrutkar*, Smita S Aher and R S Bachhav. Stability Indicating RP-HPLC Method Development and Validation for Estimation of Safinamide in Bulk Drug and Dosage Form (Research Article). 2022; 12(4): 92-106.