RP-HPLC method development and validation of Selegiline hydrochloride in nanoemulsion formulation

Authors

  • Sonal Setya Research Scholar, Uttrakhand Technical University, Dehradun, Uttrakhand
  • Bal Krishan Razdan Professor, Uttrakhand Technical University, Dehradun, Uttrakhand
  • Sushama Talegaonkar Assistant Professor, Department of Pharmaceutics, Jamia Hamdard, New Delhi

Keywords:

Selegiline hydrochloride, nanoemulsion, RPHPLC, retention time

Abstract

A simple, specific, precise and accurate RPHPLC method has been developed for determination of Selegiline hydrochloride in bulk and nanoemulsion formulation using C18 column;250 mm length, 4.6 mm internal diameter,0.5µ particle size with UV visible detector (detection wavelength206nm). The elution was performed in an isocratic mode with mobile phase consisting of methanol: phosphate buffer (95:5) at a flow rate of 1ml/minute. Methanol was used as a diluent and retention time was found to be 2.9 minutes. The method was found to be linear (20 to 160µg/ml), rugged and robust with LOQ of 0.00819 µg/ml. The percentage purity of Selegiline hydrochloride in nanoemulsion formulation was found to be 98.9%.

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Published

2015-04-01

How to Cite

Sonal Setya, Bal Krishan Razdan, & Sushama Talegaonkar. (2015). RP-HPLC method development and validation of Selegiline hydrochloride in nanoemulsion formulation. World Journal of Pharmaceutical Sciences, 3(4), 737–742. Retrieved from https://wjpsonline.com/index.php/wjps/article/view/hplc-method-selegiline-nanoemulsion-formulation

Issue

Section

Research Article