首页> 外文期刊>Analytical and bioanalytical chemistry >A rapid analytical method for cholecalciferol (vitamin D _3) in fortified infant formula, milk and milk powder using Diels-Alder derivatisation and liquid chromatography-tandem mass spectrometric detection
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A rapid analytical method for cholecalciferol (vitamin D _3) in fortified infant formula, milk and milk powder using Diels-Alder derivatisation and liquid chromatography-tandem mass spectrometric detection

机译:Diels-Alder衍生化和液相色谱-串联质谱检测法快速分析强化婴儿配方奶粉,牛奶和奶粉中的胆钙化固醇(维生素D _3)

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摘要

A method for analysing vitamin D _3 (VD3, cholecalciferol) has been established and validated. This method is rapid and cost effective and is intended for use in quality control in the manufacture of fortified infant formulae and milk powders. Milk or reconstituted milk powder was solubilised in methanol and extracted in one step into isooctane, which was separated by centrifugation. A portion of the isooctane layer was then transferred, and an aliquot of 4-phenyl-1,2,4-triazoline-3,5-dione was added to derivatise VD3. The analyte was then re-extracted into a small volume of acetonitrile and analysed by reverse-phase chromatography. Detection was by triple quadrupole mass spectrometer using a selective transition, m/z 560→298. An internal standard, deuterium-labelled VD3, was used to correct for losses in extraction and any variation in derivatisation and ionisation efficiencies. The method has been subjected to a single-laboratory validation and has been found to be linear, highly selective and accurate with respect to National Institute of Standards and Technology Standard Reference Material 1849, analyte spiking experiments and comparison with an LC-UV-based method. The repeatability standard deviation was 4.23 %. Significantly for routine laboratories, the method returns results within 2 h, generates minimal waste and minimises health and safety concerns to the analyst.
机译:建立并验证了一种分析维生素D _3(VD3,胆钙化固醇)的方法。该方法快速且具有成本效益,旨在用于强化婴儿配方奶粉和奶粉生产中的质量控制。将牛奶或重构的奶粉溶解在甲醇中,一步提取到异辛烷中,通过离心分离。然后转移一部分异辛烷层,并加入4-苯基-1,2,4-三唑啉-3,5-二酮的等分试样以使VD3衍生化。然后将分析物重新萃取到少量乙腈中,并通过反相色谱法进行分析。通过三重四极杆质谱仪使用选择性过渡m / z 560→298进行检测。使用氘标记的内标VD3来校正萃取损失以及衍生化和电离效率的任何变化。该方法已经过单实验室验证,并且相对于美国国家标准技术研究院标准参考材料1849,分析物掺入实验以及与基于LC-UV的方法进行比较,发现该方法是线性的,高度选择性和准确的。重复性标准偏差为4.23%。对于常规实验室而言,该方法的重要意义在于,该方法可在2小时内返回结果,产生最少的浪费,并使分析人员对健康和安全的担忧降至最低。

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