Development and validation of UV-spectrophotometric method for the determination of folic acid in bulk and tablet dosage forms

  • Elkhazein T
  • Abdeljabar T
  • Abdelrahman A
  • et al.
N/ACitations
Citations of this article
23Readers
Mendeley users who have this article in their library.

Abstract

Received: 23 rd November 2021 The purpose of this study was to create and verify a simple and accurate UV-Spectrophotometric technique for determining Folic acid in bulk and tablet dosage form. The approach was based on the measurement of folic acid solution absorbance at 255nm in 0.01 M NaOH. In the concentration range of 10-50 g/ml, the constructed calibration curve was found to be linear (R 2 = 0.9996). Limits of detection and quantification were 2.73 µg/ml, and 8.27 µg/ml, respectively. The precision of the developed method was confirmed by the obtained low RSD% values. Recoveries percentages were found 98.46%±1.42, 100.0%±0.20, 98.92%±1.12; n=3 for 50%, 100% and 150% levels, respectively indicating the method accuracy and freedom of interference from excipients. Folic acid content percent in the two analyzed brands were found to be equal 96.59%±0.005; n=3, and 97.28%±0.003; n=3 which complies with the official range (90-110%).

Cite

CITATION STYLE

APA

Elkhazein, T. A., Abdeljabar, T. A., Abdelrahman, A. N., Adam, M. E., & Shantier, S. W. (2022). Development and validation of UV-spectrophotometric method for the determination of folic acid in bulk and tablet dosage forms. Journal of Applied Pharmaceutical Research, 10(2), 19–23. https://doi.org/10.18231/j.joapr.2022.19.23

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free