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首页> 外文期刊>Journal of AOAC International >Application of ultra-performance liquid chromatography/tandem mass spectrometry for the measurement of vitamin D in foods and nutritional supplements.
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Application of ultra-performance liquid chromatography/tandem mass spectrometry for the measurement of vitamin D in foods and nutritional supplements.

机译:超高效液相色谱/串联质谱在食品和营养补品中维生素D测定中的应用。

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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 +or- 0.012 mg/kg, an excellent agreement with the certified value of 0.251 +or- 0.027 mg/kg. In addition, spike recovery from a commercial infant formula matrix was in the range 100-108% for both vitamins D3 and D2 at 3 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 3 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.
机译:超高效液相色谱(UPLC)/ MS / MS用于测量各种食品和营养补品中的维生素D。色谱分离的运行时间从HPLC / MS / MS中的20分钟减少到UPLC / MS / MS中的10分钟,同时获得了相同或更好的分离效率以处理复杂的食品基质。在优化的条件下,将维生素D3,D2和同位素标记的维生素D3的所有前维生素与它们相应的维生素进行基线分离。还证明了可以干扰分析的复杂食品基质中的许多固醇异构体可以与分析物很好地分离。通过分析NIST SRM 1849婴儿配方食品参考材料评估该方法的准确性。重复八次,平均维生素D3浓度为0.251±0.012 mg / kg,与标准值0.251±0.027 mg / kg达成了极好的一致性。此外,在三种加标浓度水平下,维生素D3和D2从市售婴儿配方奶粉中的加标回收率在100-108%的范围内。甚至更复杂的基质(宠物食品)的加标回收率为101-105%。维生素D3和D2的LOQ值分别为0.026和0.033 IU / g,或溶液中的0.086和0.11 IU / ml。动态范围具有3个数量级,这使得该方法灵活,有用,可应对各种样品中较宽的维生素D浓度范围。基于更改LC分离参数和MS测量参数的结果,该方法是可靠的。这种准确可靠的维生素D方法大大提高了仪器效率和分析效率。

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