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UPLC-MS/MS 法测定食品中的叶酸:一种新型高通量定量检测方法的建立与验证;测定澳大利亚强化面包中的叶酸水平。

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.

机构信息

Food Science and Technology, School of Chemical Engineering, University of New South Wales, Sydney 2052, Australia.

出版信息

Anal Bioanal Chem. 2011 Aug;401(3):1035-42. doi: 10.1007/s00216-011-5156-3. Epub 2011 Jun 13.

Abstract

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.

摘要

建立、优化和验证了一种超高效液相色谱-串联质谱法,用于定量检测叶酸强化面包中合成叶酸(FA)(也称为蝶酰-L-谷氨酸或维生素 B9)和天然 5-甲基四氢叶酸(5-MTHF)。分析前优化的样品制备包括添加(13)C(5)标记的内标物、用α-淀粉酶和大鼠血清处理、用芳香族选择性试剂盒进行固相萃取和超滤。分析物在 Waters ACQUITY HSS T3 柱上在 6 分钟的运行时间内分离,并通过正离子电喷雾选择反应监测 MS/MS 进行分析。两种分析物的标准校准曲线在 0.018-14 μg FA/g 新鲜面包(r(2) = 0.997)和 9.3-900 ng 5-MTHF/g 新鲜面包(r(2) = 0.999)范围内呈线性。FA 和 5-MTHF 的绝对回收率分别为 90%和 76%。FA 和 5-MTHF 的日内变异系数分别为 3%和 18%。FA 的检测限为 9.0 ng/g,5-MTHF 的检测限为 4.3 ng/g,使用预提取的木薯淀粉作为空白基质确定。该方法稳定、快速、准确、灵敏,适用于多种食品基质,能够检测和定量小麦面包中天然存在的低水平 5-MTHF。本研究结果表明,澳大利亚强化面包中的 FA 范围为 79-110 μg/100 g 新鲜面包,并表明面粉可能没有规定的 FA 强化水平(200-300 μg/100 g 面粉),尽管仅凭实验面包数据无法得出明确结论,因为其他作者已经记录了不同的烘焙损失。

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