DEVELOPMENT AND VALIDATION OF UV SPECTROPHOTOMETRIC METHOD FOR THE QUANTIFICATION OF METRONIDAZOLE IN PURE AND TABLET DOSAGE FORM

Authors

  • MUJITAPHA F.M. Department of Pharmaceutical and Medicinal Chemistry, Ahmadu Bello University Zaria.
  • USMAN, M.A. Department of Pharmaceutical and Medicinal Chemistry, Ahmadu Bello University Zaria.
  • YAKASAI, I.A. Department of Pharmaceutical and Medicinal Chemistry, Ahmadu Bello University Zaria.

Keywords:

Metronidazole, UV Spectrophotometric, method development, method validation, invitro dissolution

Abstract

Three simple, rapid and accurate spectrophotometric methods were developed for quantification
of metronidazole in pure and tablet dosage form. The methods involved measurement of
absorbance at wavelengths 295, 345 and 350 nm for pH 1.2, 4.5 and 6.8 respectively. The methods
were validated according to ICH guidelines with respect to different analytical parameters;
linearity, precision, accuracy and percentage recovery, Limit of detection (LOD) and Limit of
quantification (LOQ). Beer-Lambert’s law was obeyed within the concentration range of 2-
64μg/mL. The Limit of detection and quantification values were determined to be 0.0122 and
1.1154, 0.0185 and 1.6935, 0.0858 and 0.26026 for pH 1.2, 4.5, and 6.8 respectively. The proposed
methods were found to be precise since coefficient of variation (% RSD) values were less than 15
% and recovery values were found to be in the range of 95.71-100.71 %. The developed methods
were successfully used for in-vitro dissolution of Metronidazole.

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Published

2020-01-13

How to Cite

MUJITAPHA F.M., USMAN, M.A., & YAKASAI, I.A. (2020). DEVELOPMENT AND VALIDATION OF UV SPECTROPHOTOMETRIC METHOD FOR THE QUANTIFICATION OF METRONIDAZOLE IN PURE AND TABLET DOSAGE FORM. BIMA JOURNAL OF SCIENCE AND TECHNOLOGY (2536-6041), 3(02), 179-186. Retrieved from https://journals.gjbeacademia.com/index.php/bimajst/article/view/159