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首页> 外文期刊>Journal of AOAC International >Interlaboratory Comparison for the Determination of 24,25-Dihydroxyvitamin D-3 in Human Serum Using Liquid Chromatography with Tandem Mass Spectrometry
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Interlaboratory Comparison for the Determination of 24,25-Dihydroxyvitamin D-3 in Human Serum Using Liquid Chromatography with Tandem Mass Spectrometry

机译:用液相色谱法测定串联质谱法测定人血清中24,25-二羟基乙多素D-3的互责任比较

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摘要

Six laboratories associated with the Vitamin D Standardization Program (VDSP) participated in an interlaboratory comparison of LC with tandem MS (MS/MS) methods for the determination of 24,25-dihydroxyvitamin D-3 [24,25(OH)(2)D-3] in human serum. The laboratories analyzed two different serum-based Standard Reference Materials (SRMs) intended for use in the determination of 25-hydroxyvitamin D and 30 samples from the Vitamin D External Quality Assessment Scheme (DEQAS). All laboratory methods for 24,25(OH)(2)D-3 were based on isotope dilution LC-MS/MS; three of the methods used derivatization of the vitamin D metabolites before LC-MS/MS. Laboratory results were compared to the National Institute of Standards and Technology (NIST) results, which were obtained using their newly developed candidate reference measurement procedure for 24,25(OH)(2)D-3. Laboratory results for the SRM samples varied in comparability to the NIST results, with one laboratory in excellent agreement (-1.6% mean bias), three laboratories at 10-15% mean bias, and the remaining laboratory at 36% mean bias. For the 30 DEQAS samples, the mean bias for the five laboratories ranged from 6 to 15%; however, the SD of the bias ranged from 8 to 29%. As a result of this intercomparison study, one laboratory discovered and corrected a method calculation error and another laboratory modified and improved their LC-MS/MS method.
机译:与维生素D标准化程序(VDSP)相关的六个实验室参与了LC的串联比较,用于测定24,25-二羟基维生素D-3的方法[24,25(OH)(2) D-3]在人体血清中。实验室分析了两种不同的基于血清基标准参考材料(SRMS),用于测定25-羟基乙多二和30种来自维生素D外部质量评估计划(DEQAS)的样品。所有实验室方法24,25(OH)(2)D-3基于同位素稀释LC-MS / MS;三种方法使用了LC-MS / MS之前维生素D代谢物的衍生化。实验室结果与国家标准和技术研究所(NIST)结果进行了比较,这些结果是使用其新开发的候选参考测量程序获得的24,25(OH)(2)D-3获得。 SRM样品的实验室结果与NIST结果的可比性变化,一个实验室具有优异的一致性(-1.6%的平均偏见),三个实验室的平均偏差为10-15%,剩余的实验室平均偏差。对于30个Deqas样本,五个实验室的平均偏差范围为6%至15%;然而,偏差的SD范围为8〜29%。由于这种离上的研究,发现并纠正了方法计算误差和另一种实验室修改并改善了它们的LC-MS / MS方法。

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