Development and validation of naproxen in bulk and tablet dosage form

Authors

  • Afshanurooj Nalanda College of Pharmacy, Cherlapally, Nalgonda, Telangana, India
  • N. Balaraju Nalanda College of Pharmacy, Cherlapally, Nalgonda, Telangana, India
  • B. Swathi Nalanda College of Pharmacy, Cherlapally, Nalgonda, Telangana, India
  • P. Sainath Nalanda College of Pharmacy, Cherlapally, Nalgonda, Telangana, India
  • D. Vijaya Laxmi Nalanda College of Pharmacy, Cherlapally, Nalgonda, Telangana, India
  • Rajeswar Dutt Nalanda College of Pharmacy, Cherlapally, Nalgonda, Telangana, India
  • K.N.V. Rao Nalanda College of Pharmacy, Cherlapally, Nalgonda, Telangana, India

Keywords:

Naproxen, Spectrophotometric, Correlation coefficient, Regression method, Standard deviation

Abstract

A simple, accurate, precise and sensitive UV-Spectrophotometric method was developed for the determination of naproxen. The solvent used was ethanol and the wavelength corresponding to maximum absorbance of the drug was found at 242 nm. Beer’s law was obeyed in the concentration range of 10-60 µg/mL with correlation coefficient of 0.9984. The method was validated for several parameters like linearity and range, accuracy, precision and specificity as per International Conference on Harmonization guidelines. The value of the relative standard deviation and %recovery was found to be satisfactory, indicating that the proposed method is precise and accurate and hence can be used for the routine analysis of naproxen.

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Published

2019-05-01

How to Cite

Afshanurooj, N. Balaraju, B. Swathi, P. Sainath, D. Vijaya Laxmi, Rajeswar Dutt, & K.N.V. Rao. (2019). Development and validation of naproxen in bulk and tablet dosage form. World Journal of Pharmaceutical Sciences, 7(5), 95–101. Retrieved from https://wjpsonline.com/index.php/wjps/article/view/development-validation-spectrophotometric-naproxen

Issue

Section

Research Article

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