LC Method Development and Validation for the Determination of Ropivacaine Hydrochloride in Bulk Drug and Pharmaceutical Formulations

• Published in: Pharmaceutical Chemistry Journal
• Main Author: Chigurupati S.; Appala R.N.; Selvarajan K.K.; Khaw C.H.; Teoh C.F.; Batumanathan L.; Mohammad J.I.
• Format: Retracted
• Language: English
• Published: Springer Science and Business Media, LLC 2017
• Online Access: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017478790&doi=10.1007%2fs11094-017-1561-z&partnerID=40&md5=7043431c81656edaf92a7b61b4e5d20b

Asimple liquid chromatography method has been developed for the assay of ropivacaine hydrochloride in raw material and final products. The chromatographic separation employs gradient elution using C8 column, mobile phase consisting of solvent [A] (monobasic phosphate buffer adjusted to pH 2.5) and solvent [B] (acetonitrile) delivered at a flow rate of 1.0 mL/min. The analytes were detected at 220 nm and peak purity was examined using a photodiode array detector. The proposed method was validated to demonstrate its selectivity, accuracy, precision, robustness, and linearity within a given range. The limits of detection and quantitation were 0.1 and 0.5 g/mL, respectively. The specificity of the method was investigated under various stress conditions, including hydrolysis, heat, oxidation, and photolysis. Stress testing showed degradants, which were well separated from the parent compound proving the stability and indicating capacity of the method. © 2017, Springer Science+Business Media New York.