Development and validation of a method for the determination of folic acid in different pharmaceutical formulations using derivative spectrophotometry

被引:6
|
作者
de Moura Ribeiro, Marcos Vinicius [1 ,2 ]
Melo, Ingrid da Silva [2 ]
da Costa Lopes, Francisco das Chagas [2 ]
Moita, Graziella Ciaramella [2 ]
机构
[1] UNESP, Sao Paulo State Univ Julio Mesquita Filho, Inst Chem, Araraquara, SP, Brazil
[2] Univ Fed Piaui, Ctr Nat Sci, Dept Chem, Teresina, PI, Brazil
关键词
Folic acid/pharmaceutical formulations; Folic acid/pharmaceutical formulations/validation method; Folic acid/formulations/derivative spectrophotometry; NEURAL-TUBE DEFECTS; CARBON NANOTUBES; PASTE ELECTRODE; URIC-ACID; FORTIFICATION; FOOD; CHROMATOGRAPHY; METHOTREXATE; TABLETS; SENSOR;
D O I
10.1590/S1984-82502016000400019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Folic acid is a B complex water-soluble vitamin that is essential to humans, and its deficiency can cause problems including congenital malformations in the fetus as well as heart disease. Most countries affected by diseases associated with a lack of folic acid now supplement foods with the vitamin. There is therefore a need for the development of new analytical procedures able to determine folic acid present in different matrices. This work describes the development of zero order and first order derivative spectrophotometric methods for the determination of folic acid in different pharmaceutical formulations, using 0.1 mol L-1 NaOH as solvent. The methods are shown to be simple, selective, and robust. Good linearity was achieved, with correction coefficients >= 0.9996 and limits of detection and quantification ranging from 0.64 to 0.75 and from 1.80 to 2.85 mg L-1, respectively. Recoveries of 98-104% were obtained in accuracy tests, and precision (as RSD) was between 0.2 and 4.8%. The methods can be used in routine analyses for quality control purposes, offering an alternative to the procedures already reported in the literature.
引用
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页码:741 / 750
页数:10
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