Fonterra Co-operative Group Ltd, P.O. Box 7, Waitoa, 3341, New Zealand.
J AOAC Int. 2020 Jun 1;103(3):812-817. doi: 10.1093/jaoacint/qsz034.
Thiamine and pantothenic acid play a critical role in numerous metabolic reactions and are typically supplemented in infant and adult nutritional formulas as thiamine chloride hydrochloride and calcium pantothenate salts.
A rapid compliance method for the analysis of thiamine and pantothenic acid applicable to infant formula and milk-based nutritional products is described.
Proteins are removed by centrifugal ultrafiltration, followed by analysis by reversed-phase liquid chromatography‒tandem mass spectrometry (LC-MS/MS), with quantitation accomplished by internal standard technique.
The method was shown to be accurate, with acceptable recovery (thiamine, 99.3-101.1%; pantothenic acid, 99.2-108.6%). A certified reference material (NIST 1849a), showed no statistical bias (α = 0.05) for thiamine (P = 0.64); although a statistically significant bias (P < 0.01) for pantothenic acid was found, the nominal bias was only 4.7% (mean = 7.1 mg/hg; certified value = 6.8 mg/hg). A comparison of results by LC-MS/MS and current methods showed negligible bias (mean bias: thiamine, 0.01 mg/hg; pantothenic acid, 0.17 mg/hg) and no statistical significance (α = 0.05; thiamine, P = 0.399; pantothenic acid, P = 0.058). Acceptable precision was demonstrated with a repeatability of 7.2% repeatability relative standard deviation (RSDr) (HorRat: 0.6) and an intermediate precision of 7.0% RSD for thiamine, and a repeatability of 5.7% RSDr (HorRat: 0.5) and an intermediate precision of 6.1% RSD for pantothenic acid.
This rapid method is intended for use in high-throughput laboratories as part of routine product compliance release testing of thiamine and pantothenic acid in manufactured infant and milk-based nutritional products.
硫胺素和泛酸在许多代谢反应中起着关键作用,通常以盐酸硫胺素和泛酸钙盐的形式补充到婴儿和成人营养配方中。
描述一种适用于婴儿配方食品和乳基营养产品的快速合规性分析方法,用于检测硫胺素和泛酸。
通过离心超滤去除蛋白质,然后通过反相液相色谱-串联质谱(LC-MS/MS)进行分析,通过内标技术进行定量。
该方法被证明是准确的,回收率可接受(硫胺素,99.3-101.1%;泛酸,99.2-108.6%)。对认证参考物质(NIST 1849a)进行测试,结果显示硫胺素没有统计学偏差(α=0.05;P=0.64);尽管发现泛酸有统计学上显著的偏差(P<0.01),但名义偏差仅为 4.7%(平均值=7.1mg/hg;认证值=6.8mg/hg)。通过 LC-MS/MS 与现行方法的比较结果表明,偏差可忽略不计(硫胺素平均偏差:0.01mg/hg;泛酸平均偏差:0.17mg/hg),且无统计学意义(α=0.05;硫胺素,P=0.399;泛酸,P=0.058)。该方法重复性良好,精密度可接受,硫胺素的重复性相对标准偏差(RSDr)为 7.2%(HorRat:0.6),中间精密度为 7.0%RSD;泛酸的重复性 RSDr 为 5.7%(HorRat:0.5),中间精密度为 6.1%RSD。
该快速方法旨在用作高通量实验室的一部分,用于常规产品放行测试,以检测制造的婴儿和乳基营养产品中硫胺素和泛酸的含量。