Stability indicating RP-HPLC method development and validation of Terbinafine in pure and pharmaceutical formulations

Authors

  • Byasabhusan Das Professor and HOD, Department of Pharmaceutical Analysis, Anwarul Uloom College of Pharmacy, Hyderabad, Telangana
  • Paul Richards M Professor, Department of Pharmaceutical Chemistry, Aditya Bangalore Institute of Pharmacy Education and Research, Yelahanka, Kogilu, Bangalore -64, India
  • B. A. Vishwanath Principal and Chairman, Department of Pharmaceutics, Aditya Bangalore Institute of Pharmacy Education and Research, Yelahanka, Kogilu, Bangalore -64, India
  • Suchitra D Professor, Department of Pharmaceutical Chemistry, Department of Pharmaceutics, Aditya Bangalore Institute of Pharmacy Education and Research, Yelahanka, Kogilu, Bangalore -64, India
  • Najma Amreen Research Scholar, Department of Pharmaceutical Analysis, Anwarul Uloom College of Pharmacy, Hyderabad, Telangana

Keywords:

Terbinafine HCl, Stability Studies, HPLC

Abstract

A high performance liquid chromatographic strategy for the assessment of Terbinafine HCl from formulation was created. Terbinafine HCl was chromatographed on a BDS Hypersil C18 column 150 cm long and having an inner measurement of 4.6 mm. Mobile phase involving Mobile phase A - Buffer of K2HPO4, Mobile phase B of Methanol, Mobile phase C of Acetonitrile within the volume proportion of 15:35:50. The pH of the buffer adjusted to7.5. The detection was carried out using an ultraviolet detector set at a wavelength of 223 nm. The technique was extended for the stability studies of Terbinafine HCl.

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Published

2020-11-30

How to Cite

Byasabhusan Das, Paul Richards M, B. A. Vishwanath, Suchitra D, & Najma Amreen. (2020). Stability indicating RP-HPLC method development and validation of Terbinafine in pure and pharmaceutical formulations. World Journal of Pharmaceutical Sciences, 8(12), 102–106. Retrieved from https://wjpsonline.com/index.php/wjps/article/view/stability-indicating-rp-hplc-terbinafine

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Research Article

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