A UV spectrophotometric method for the determination of folic acid in pharmaceutical tablets and dissolution tests


Journal article


R. Matias, P. S. R. Ribeiro, M. Sarraguça, J. Lopes
2014

Semantic Scholar DOI
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APA   Click to copy
Matias, R., Ribeiro, P. S. R., Sarraguça, M., & Lopes, J. (2014). A UV spectrophotometric method for the determination of folic acid in pharmaceutical tablets and dissolution tests.


Chicago/Turabian   Click to copy
Matias, R., P. S. R. Ribeiro, M. Sarraguça, and J. Lopes. “A UV Spectrophotometric Method for the Determination of Folic Acid in Pharmaceutical Tablets and Dissolution Tests” (2014).


MLA   Click to copy
Matias, R., et al. A UV Spectrophotometric Method for the Determination of Folic Acid in Pharmaceutical Tablets and Dissolution Tests. 2014.


BibTeX   Click to copy

@article{r2014a,
  title = {A UV spectrophotometric method for the determination of folic acid in pharmaceutical tablets and dissolution tests},
  year = {2014},
  author = {Matias, R. and Ribeiro, P. S. R. and Sarraguça, M. and Lopes, J.}
}

Abstract

Folic acid (FA) or pteroyl-L-glutamic acid, chemically known as N-[4-[[(2-amino-1,4-dihydro-4-oxo-6-pteridinyl)methyl]amino]benzoyl]-L-glutamic acid, is a water-soluble B vitamin that helps build healthy cells. In this study, a new, simple, easy, accurate, precise, economic and sensitive UV spectrophotometric method for the determination of folic acid in commercial tablets and during dissolution tests is presented. Using a phosphate buffer solution at pH 9.0 it was possible to determine the concentration of folic acid in commercial tablets at a λmax of 282.5 nm in a linear range of 1.0–17.5 μg ml−1 with a R2 > 0.9999 and recovery between 100.6 and 101.1%. The method was also optimized for the quantification of folic acid in dissolution tests in the same linear concentration range. The pH effect on the UV spectra of folic acid solutions was eliminated with a first derivative. This procedure allowed the direct measurement of samples from the dissolution vessel (pH approximately equal to 6) without any pH correction. This method was based on the first derivative of the absorbance at λ = 377.2 nm, yielding an R2 > 0.9997 with recovery percentages similar to those presented before. The statistical comparison between the proposed and the HPLC reference method showed excellent agreement and indicates no statistically significant difference in accuracy and precision at a 0.05 significance level.


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