Determination of Folic Acid by Ultra-High Performance Liquid Chromatography in Certain Malt-based Beverages after Solid-Phase Extraction

Elif Mine Öncü-Kaya
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引用次数: 2

Abstract

The aim of the present work was to develop and validate an efficient Ultra-High Performance Liquid Chromatography (UHPLC) method for the determination of folic acid (FA) in malt-based beverages. Solid-phase extraction (SPE) procedure was used for cleanup and preconcentration of the malt-based beverages before the UHPLC analysis. The analysis was performed in a C18 column (2.1x50 mmx1.8 µm) using a solvent system of ACN: 0.1 % formic acid in water (10:90, v/v) by isocratic elution. Injection volume was 5 µL. The flow rates of the mobile phase were maintained at 0.2 mL min ‒1 for 0.00–4.00 min and 0.5 mL min ‒1 for 4.01–12.00 min. Methyl paraben was used as the internal standard (IS). The FA and IS signals were detected at 284 nm and 254 nm, respectively. Under these conditions, FA and IS were separated in 3.6 min and 11.4 min, respectively. The method was successfully validated in terms of precision, accuracy, linearity, limits of detection (LOD) and quantification (LOQ) parameters. The relative standard deviations for intra- and inter-day precision were less than 1.5%. Good linearity with a high correlation coefficient was achieved over the concentration range of 20.13 µg L −1 – 2004 µg mL −1 for FA. The LOD and LOQ values were 6.66 µg L −1 and 20.13 µg L −1 , respectively . Good recovery values were found ranged between 99.1% and 106% for boza and vitamin fortified malt drink. The proposed method was successfully applied for the determination of FA in malt beers, vitamin fortified malt drinks and boza samples.
超高效液相色谱法测定某些麦芽饮料中叶酸的固相萃取
本研究的目的是建立一种高效液相色谱法(UHPLC)测定麦芽饮料中叶酸的方法。在UHPLC分析之前,采用固相萃取法(SPE)对麦芽饮料进行清洗和预浓缩。色谱柱为C18 (2.1x50 mmx1.8µm),溶剂体系为ACN: 0.1%甲酸水溶液(10:90,v/v),等密度洗脱。注射量为5µL。流动相流速为0.2 mL min -1,流速为0.00-4.00 min,流速为0.5 mL min -1,流速为4.01-12.00 min。内标为对羟基苯甲酸甲酯。FA和IS信号分别在284 nm和254 nm处检测到。在此条件下,FA和IS的分离时间分别为3.6 min和11.4 min。从精密度、准确度、线性度、检出限和定量参数等方面对该方法进行了验证。日内、日间精度的相对标准偏差均小于1.5%。FA在20.13µg L−1 ~ 2004µg mL−1的浓度范围内具有良好的线性关系,相关系数高。LOD和LOQ值分别为6.66µg L−1和20.13µg L−1。boza和维生素强化麦芽饮料的回收率在99.1% ~ 106%之间。该方法已成功地应用于麦芽啤酒、维生素强化麦芽饮料和boza样品中FA的测定。
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