All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Abstract

Development and validation of reverse-phase high-performance liquid chromatography method for estimation of citicoline sodium in bulk and dosage form

Author(s): HK Maradiya1, Vasundhara H Pansara2
1Department of Pharmaceutical Quality Assurance, Veerayatan Institute of Pharmacy, Jakhania-370 460, India 2Department of Pharmaceutical Quality Assurance, N.R.Vekaria Institute of Pharmacy and Research Centre, India

Correspondence Address:
H K Maradiya Department of Pharmaceutical Quality Assurance, Veerayatan Institute of Pharmacy, Jakhania-370 460 India E-mail: hitu.pharma87@gmail.com


A simple, accurate, precise and sensitive reverse-phase high-performance liquid chromatography method for the determination of citicoline sodium has been developed and validated. Drug was resolved on a C18 column (Phenomenex Luna, 250×4.6 mm, 10μ), utilizing mobile phase of potassium dihydrogen phosphate buffer and acetonitrile in a ratio of 30:70. Mobile phase was delivered at the flow rate of 1.0 ml/min and detection was carried out at 272 nm. Separation was completed within 2.22 min. Calibration curve was linear with good correlation coefficient (R 2 =0.999) over a concentration range 10-60 μg/ml. Recovery was between 98.84 and 101.76%. Method was found to be reproducible with relative standard deviation for intra and interday precision of <2.0% over the said concentration range. The method was successfully applied to the determination of the citicoline sodium, it can be very useful and an alternate to performing the stability studies.

Full-Text | PDF

 
 
Google scholar citation report
Citations : 69022

Indian Journal of Pharmaceutical Sciences received 69022 citations as per google scholar report