Method development and validation of RP-HPLC Method for determination of new Antipsychotic agent in Paliperidone Palmitate bulk drug

Abstract

A simple, precise, rapid ,reproducible, accurate and stability indicating RP-HPLC method has been developed for the determination of new antipsychotic agent paliperidone in pharmaceutical formulation. zorbax –SB-phenyl, 150x4.6mm; 3.5µm particle size column was used with variable wavelength UV detector. The mobile phase consisting of PH 4 Buffer and Acetonitrile 80:20 v/v was used. The flow rate was 1 ml/min and the effluent was monitored at 238 nm. The retention time of drug was 0.9. The method was linear over the concentration range of 1.0 mg/ml. The method precision for the determination of assay was below 2%RSD. The percentage recovery of paliperidone was 85-115%. The validation of method was carried out utilizing ICH Q2 (R1) guidelines.

Authors and Affiliations

G. Swarnalatha , B. Vijayakumar , D. Jothieswari , P. Jaya Chandra Reddy , M. Mohankumar

Keywords

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  • EP ID EP107241
  • DOI -
  • Views 88
  • Downloads 0

How To Cite

G. Swarnalatha, B. Vijayakumar, D. Jothieswari, P. Jaya Chandra Reddy, M. Mohankumar (2014). Method development and validation of RP-HPLC Method for determination of new Antipsychotic agent in Paliperidone Palmitate bulk drug. International Journal of Novel Trends in Pharmaceutical Sciences, 4(5), 101-110. https://europub.co.uk./articles/-A-107241