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Folate analysis in foods by UPLC-MS/MS: Development and validation of a novel, high throughput quantitative assay; Folate levels determined in Australian fortified breads

机译:通过UPLC-MS / MS对食品中的叶酸进行分析:新型高通量定量分析的开发和验证;澳大利亚强化面包中的叶酸含量测定

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摘要

An ultra-performance liquid chromatography-tandem mass spectrometry method was developed, optimised and validated for the quantification of synthetic folic acid (FA), also called pteroyl-l-glutamic acid or vitamin B9 and naturally occurring 5-methyltetrahydrofolate (5-MTHF) found in folate-fortified breads. Optimised sample preparation prior to analysis involved addition of ~(13)C_5 labelled internal standards, treatments with α-amylase and rat serum, solid-phase extraction using aromatic-selective cartridges and ultra-filtration. Analytes were separated on a Waters ACQUITY HSS T3 column during a 6-min run and analysed by positive ion electrospray selected reaction monitoring MS/MS. Standard calibration curves for the two analytes were linear over the range of 0.018-14 μg FA/g of fresh bread (r 2∈=∈0.997) and 9.3-900 ng 5-MTHF/g of fresh bread (r 2∈=∈0.999). The absolute recoveries were 90% and 76% for FA and 5-MTHF, respectively. Intra-day coefficients of variation were 3% for FA and 18% for 5-MTHF. The limit of detection was 9.0 ng/g for FA and 4.3 ng/g for 5-MTHF, determined using pre-extracted tapioca starch as the blank matrix. The assay is rugged, fast, accurate and sensitive, applicable to a variety of food matrices and is capable of the detection and quantification of the naturally occurring low levels of 5-MTHF in wheat breads. The findings of this study revealed that the FA range in Australian fortified breads was 79-110 μg/100 g of fresh bread and suggest that the flour may not have the mandated FA fortification level (200-300 μg/100 g of flour), though this cannot be determined conclusively from experimental bread data alone, as variable baking losses have been documented by other authors.
机译:开发,优化和验证了一种超高效液相色谱-串联质谱法,用于定量合成叶酸(FA)(也称为蝶酰基-1-谷氨酸或维生素B9)和天然存在的5-甲基四氢叶酸(5-MTHF)在叶酸强化面包中发现。分析之前优化的样品前处理包括添加〜(13)C_5标记的内标物,用α-淀粉酶和大鼠血清处理,使用芳香族选择性滤芯的固相萃取和超滤。在6分钟的运行过程中,在Waters ACQUITY HSS T3色谱柱上分离了分析物,并通过正离子电喷雾选择的反应监测MS / MS进行了分析。两种分析物的标准校准曲线在0.018-14μgFA / g新鲜面包(r2∈=∈0.997)和9.3-900 ng 5-MTHF / g新鲜面包(r2∈=∈)范围内呈线性0.999)。 FA和5-MTHF的绝对回收率分别为90%和76%。对于FA,日内变异系数为3%,对于5-MTHF为38%。使用预先提取的木薯淀粉作为空白基质测定的FA的检出限为9.0 ng / g,5-MTHF的检出限为4.3 ng / g。该测定法坚固耐用,快速,准确和灵敏,适用于各种食品基质,并且能够检测和定量小麦面包中天然存在的低水平的5-MTHF。这项研究的结果表明,澳大利亚强化面包的FA范围为79-110μg/ 100 g新鲜面包,这表明面粉可能没有法定的FA强化水平(200-300μg/ 100 g面粉),尽管不能单独从实验面包数据中得出结论,但其他作者已记录了可变的烘烤损失。

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