A validated reverse phase hplc method for the simultaneous estimation of clopidogrel bisulfate and rivaroxaban in pharmaceutical application

Authors

  • Rupali Sajjanwar Prist University, Thanjavur Road, Vallam, Tamil Nadu 613403
  • Shyamala Bhaskaran Prist University, Thanjavur Road, Vallam, Tamil Nadu 613403
  • Kulesh Kakati Prist University, Thanjavur Road, Vallam, Tamil Nadu 613403
  • Shailendra Kumar Jha Prist University, Thanjavur Road, Vallam, Tamil Nadu 613403

Abstract

A simple, sensitive and precise reverse phase high performance liquid chromatographic method has been developed for the simultaneous estimation of Clopidogrel bisulfate and rivaroxaban in pharmaceutical dosage forms. The combination drug was analyzed on BDS hypersil C18, 250mm × 4.6mm, 5µ, Thermo scientific. Mobile phase consisted of  buffer (0.05M KH2PO4 pH 4.0) : methanol in the ratio of 30:70 v/v delivered at a flow rate of 1.0 ml / min and wavelength of detection at 220 nm. The retention times of Clopidogrel bisulfate and Rivaroxaban were 2.39 min and 4.04 min respectively. The developed method was validated according to ICH guidelines. The proposed method can be used for the determination of these drugs in combined dosage forms.

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Published

2015-11-30

How to Cite

Sajjanwar, R., Bhaskaran, S., Kakati, K., & Jha, S. K. (2015). A validated reverse phase hplc method for the simultaneous estimation of clopidogrel bisulfate and rivaroxaban in pharmaceutical application. Journal of Applied Pharmaceutical Research, 3(3), 09-16. Retrieved from https://japtronline.com/index.php/joapr/article/view/55

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