Development and validation of a high performance liquid chromatography method for the determination of vitamin C in survival tablets
Main Article Content
Abstract
This study was conducted to develop and validate a high performance liquid chromatography (HPLC) method for the quantification of vitamin C in survival tablets. The optimized chromatographic conditions consisted of a C18 (250 x 4,6 mm, 5µm) column, a mobile phase of water containing 0,1% acetic acid and methanol (90 : 10, v/v), a flow rate of 0,5 mL/min, an injection volume of 10 µL, and a detection wavelength of 245 nm. Samples were processed by single ultrasonic extraction with a 0,1% TFA solution in water for 15 minutes. The method was validated according to ICH guidelines and showed good system suitability and high specificity. The method exhibited a linear range of 0,25 – 500 µg/mL with a correlation coefficient R2 = 0.9999. The limit of detection (LOD) and the limit of quantification (LOQ) were 0,10 µg/mL and 0,25 µg/mL, respectively. The precision of the method was satisfactory, with intra–day and inter–day RSD values below 2%, and recovery rates ranging from 95 to 105% (RSD < 2%). These results confirm that the method is suitable for the determination of vitamin C content in survival tablets.
Article Details
Keywords
Survival tablets, vitamin C, HPLC, method validation
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