Simultaneous determination of levocetrizine and phenylpropanolamine hydrocholride by RP-HPLC

Authors

  • A. Srinivasan Department of Pharmaceutical Analysis, Jaya College of Paramedical Sciences, College of Pharmacy, Chennai-602024, Tamil Nadu, India. Author
  • P. Divakar Department of Pharmaceutical Analysis, Jaya College of Paramedical Sciences, College of Pharmacy, Chennai-602024, Tamil Nadu, India. Author
  • A. Maheswaran Department of Pharmaceutical Analysis, Jaya College of Paramedical Sciences, College of Pharmacy, Chennai-602024, Tamil Nadu, India. Author
  • D. Saravanan Department of Pharmaceutical Analysis, Jaya College of Paramedical Sciences, College of Pharmacy, Chennai-602024, Tamil Nadu, India. Author

DOI:

https://doi.org/10.33974/ijrpst.v2i2.238

Abstract

The aim of the present study was to develop the simple, selective, rapid, precise and economical reverse phase-high performance liquid chromatography (RP-HPLC) method for the simultaneous estimation of levocetirizine and phenylpropanolamine HCl in solid dosage forms. The method was carried out on a Phenomenex Luna C18 (25 cm × 4.6 mm i.d., 5 μ) column with a mobile phase consisting of acetonitrile: 0.5% triethylamine (70:30 v/v, pH 3.0) at a flow rate of 1.2 mL/min. Detection was carried out at 220 nm. The retention time (RT) 1.8 min and 2.6 min for phenylpropanolamine hydrocholride and levocetrizine respectively. The % recovery of standard phenylpropanolamine hydrocholride and levocetrizine was found to be 98.17 to 103.56 and 98.893 to 10.422 respectively. The % recovery of sample phenylpropanolamine hydrocholride and levocetrizine was found to be 101.30 and 100.63 respectively. The validation of the proposed method was also carried out. The proposed method can be used for the estimation of these drugs in combined dosage forms.

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Chromatogram of LEVO and PPH

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Published

21-10-2020

Issue

Section

Research Article

How to Cite

Simultaneous determination of levocetrizine and phenylpropanolamine hydrocholride by RP-HPLC. (2020). International Journal of Research in Pharmaceutical Sciences and Technology, 2(2), 32-36. https://doi.org/10.33974/ijrpst.v2i2.238