A high-performance liquid chromatography method for simultaneous quantification of metformin and ferulic acid in solid dosage forms

被引:2
作者
Chaves Junior, Jose Venancio [1 ]
Muniz, Vanessa Morais [2 ]
Rodrigues de Almeida, Vinicius Cleithon [1 ]
de Souza, Fabio Santos [2 ]
Soares Aragao, Cicero Flavio [1 ]
机构
[1] Univ Fed Rio Grande do Norte, Pharm Dept, BR-59010115 Natal, RN, Brazil
[2] Paraiba Fed Univ, Pharmaceut Sci Dept, BR-58051970 Joao Pessoa, Paraiba, Brazil
关键词
ferulic acid; formulation; metformin; validation; RP-HPLC METHOD; HUMAN PLASMA; HYDROCHLORIDE;
D O I
10.1002/jssc.202200373
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Metformin is one of the most commonly used drugs in the world for the treatment of type 2 diabetes, while ferulic acid is a molecule that stands out for its antioxidant potential. Recent studies demonstrate hypoglycemic synergy between these molecules. The objective of this study is to develop and validate an analytical methodology by high-performance liquid chromatography for the simultaneous quantification of these drugs in pharmaceutical formulations. The method used an octadecylsilane column and a mobile phase composed of 6 mM sodium lauryl sulfate in 15 mM phosphate buffer:ACN (65:35). Ferulic acid and metformin were monitored at 232 nm, with a mobile phase flow rate of 1ml/min and oven temperature at 40 degrees C. The method was linear in the range of 5-25 mu g/ml for both molecules. In the presence of degradation products, satisfactory selectivity was achieved. Accuracy values were close to 100% and standard deviations in precision were less than 2%. In the robustness evaluation, the proposed variations did not interfere with the quantification. Therefore, it is concluded that the present method can be safely applied to the quality control of ferulic acid and metformin raw materials, as well as when they are combined in pharmaceutical formulations.
引用
收藏
页码:3866 / 3873
页数:8
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