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超高效液相色谱/串联质谱法在食品和营养补充剂中维生素D测定中的应用

Application of ultra-performance liquid chromatography/tandem mass spectrometry for the measurement of vitamin D in foods and nutritional supplements.

作者信息

Huang Min, Winters Doug

机构信息

Covance Laboratories Inc., 3301 Kinsman Blvd, Madison, WI 53704, USA.

出版信息

J AOAC Int. 2011 Jan-Feb;94(1):211-23.

PMID:21391498
Abstract

Ultra-performance liquid chromatography (UPLC)/MS/MS was applied to measure vitamin D in various foods and nutritional supplements. The run-time of the chromatographic separation was cut from 20 min in HPLC/MS/MS to 10 min in UPLC/MS/MS, while equal or better separation efficiency was achieved to deal with complex food matrixes. Under the optimized conditions, all the previtamins of vitamin D3, D2, and isotope-labeled vitamin D3 were baseline-separated from their corresponding vitamins. It was also demonstrated that many sterol isomers in complex food matrixes that interfere in the analysis could be well-separated from the analytes. Accuracy of this method was evaluated by analysis of NIST SRM 1849 infant formula reference material. With eight replicates, the average vitamin D3 concentration was 0.251 +/- 0.012 mg/kg, an excellent agreement with the certified value of 0.251 +/- 0.027 mg/kg. In addition, spike recovery from a commercial infant formula matrix was in the range of 100 to 108% for both vitamins D3 and D2 at three spike concentration levels. The spike recovery for an even more complex matrix, pet food, was 101-105%. LOQ values were 0.026 and 0.033 IU/g, or 0.086 and 0.11 IU/mL in solution, for vitamins D3 and D2, respectively. The dynamic range had three orders of magnitude, which made the method flexible and useful to deal with the wide concentration range of vitamin D in various samples. The method was robust based on the results of changing the parameters of LC separation and MS measurement. This accurate and reliable vitamin D method increased instrument efficiency and analysis productivity significantly.

摘要

采用超高效液相色谱(UPLC)/串联质谱(MS/MS)法测定各类食品和营养补充剂中的维生素D。色谱分离的运行时间从高效液相色谱/串联质谱(HPLC/MS/MS)的20分钟缩短至超高效液相色谱/串联质谱(UPLC/MS/MS)的10分钟,同时在处理复杂食品基质时实现了同等或更高的分离效率。在优化条件下,维生素D3、D2的所有前体维生素以及同位素标记的维生素D3均与相应的维生素实现了基线分离。研究还表明,复杂食品基质中许多干扰分析的甾醇异构体能够与分析物良好分离。通过分析美国国家标准与技术研究院(NIST)SRM 1849婴儿配方奶粉参考物质评估了该方法的准确性。八次重复测定结果显示,维生素D3的平均浓度为0.251±0.012毫克/千克,与认证值0.251±0.027毫克/千克高度吻合。此外,在三种加标浓度水平下,市售婴儿配方奶粉基质中维生素D3和D2的加标回收率均在100%至108%之间。对于更为复杂的宠物食品基质,加标回收率为101% - 105%。维生素D3和D2的定量限(LOQ)分别为0.026和0.033国际单位/克,或溶液中为0.086和0.11国际单位/毫升。动态范围达三个数量级,这使得该方法在处理各种样品中浓度范围广泛的维生素D时灵活且实用。基于液相色谱分离和质谱测量参数变化的结果,该方法具有稳健性。这种准确可靠的维生素D检测方法显著提高了仪器效率和分析效率。

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