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 AJAC  Vol.3 No.5 , May 2012
Development and Validation of Stability Indicating RP-LC Method for Estimation of Ranolazine in Bulk and Its Pharmaceutical Formulations
Abstract: An isocratic reverse phase liquid chromatography (RP-LC) method has been developed and subsequently validated for the determination of Ranolazine in Bulk and its pharmaceutical formulation. Separation was achieved with a X-terra RP-18 ((Make: Waters Corporation; 150 mm × 4.6 mm I.D.; particle size 5 μm)) Column and Sodium di-hydrogen phosphate monohydrate buffer with Tri ethyl amine (pH adjusted to 5.0 with diluted orthophosphoric acid): Acetonitrile (600:400) v/v as eluent at a flow rate of 1.0 mL/min. UV detection was performed at 225 nm. The method is simple, rapid, and selective. The described method of Ranolazine is linear over a range of 11.98 μg/mL to 37.92 μg/mL. The method precision for the determination of assay was below 1.0%RSD. The percentage recoveries of active pharmaceutical ingredient (API) from dosage forms ranged from 99.1% to 100.9%. The results showed that the proposed method is suitable for the precise, accurate and rapid determination of Ranolazine in bulk, its capsule dosage forms.
Cite this paper: G. Ramanaiah, D. Ramachandran, G. Srinivas, J. Gowardhane, P. Rao and S. V, "Development and Validation of Stability Indicating RP-LC Method for Estimation of Ranolazine in Bulk and Its Pharmaceutical Formulations," American Journal of Analytical Chemistry, Vol. 3 No. 5, 2012, pp. 378-384. doi: 10.4236/ajac.2012.35050.
References

[1]   www.druginfo.nlm.nih.gov

[2]   www.rxlist.com

[3]   C. Greenaway, N. Ratnaraj, J. W. Sander and P. N. Patsalos, “A High-Performance Liquid Chromatography Assay to Monitor the New Antiepileptic Drug Lacosamide in Patients with Epi-lepsy,” Therapeutic Drug Monitoring, Vol. 32, No. 4, 2010, pp. 448.doi.org/10.1097/FTD.0b013e3181dcc5fb

[4]   L. R. Snyder, J. J. Kirkland and J. L. Glajch, “Practical HPLC Method Development,” 2nd Edition, Wiley-Inter-science, New York, 1997.

[5]   United States Pharmacopeia, USP 34-NF 29, 2011.

[6]   ICH Guidelines on Validation of Analytical Procedure: Text and Methodology Q 2 (R1), 2011.

 
 
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