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首页> 外文期刊>Journal of AOAC International >Choline in infant formula and adult nutritionals by ion chromatography and suppressed conductivity: First Action 2012.20.
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Choline in infant formula and adult nutritionals by ion chromatography and suppressed conductivity: First Action 2012.20.

机译:婴幼儿配方食品和成人营养品中的胆碱通过离子色谱法和抑制电导率的作用:第一行动2012.20。

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Single-laboratory validation (SLV) data from a method for the determination of choline in infant formula and adult nutritionals by ion chromatography (IC) and suppressed conductivity were generated and presented to the Stakeholder Panel on Infant Formula and Adult Nutritionals (SPIFAN) Expert Review Panel (ERP) at the AOAC Annual Meeting held in Las Vegas, NV, during September 30 to October 3, 2012. The ERP reviewed the data and concluded that the data met the standard method performance requirements (SMPRs) established and approved the method as AOAC Official First Action. At the ERP's request, a second, full SLV was performed on 17 SPIFAN matrixes that included fortified and placebo products. Prior to IC analysis, microwave-assisted acid hydrolysis was used to digest and release bound choline from powder and ready-to-feed (RTF) infant formula and adult nutritional samples. Following hydrolysis, separation of choline from common cations was achieved on a Thermo ScientificTM DionexTM IonPacTM CS19 column followed by suppressed conductivity detection. Total choline was measured and reported as the choline ion in mg/100 g reconstituted material or RTF as-is. The system was calibrated over the analytical range specified in the SMPR (2-250 mg/100 g). Recoveries of spiked samples at 50 and 100% of the fortified choline amounts ranged from 93.1 to 100.7% with RSDs <=6.7% for product containing <2 mg/100 g and <=4.1% for product containing 2-100 mg/100 g. Accuracy for the National Institute of Standards and Technology Standard Reference Material 1849a was determined over a 6-day interval and found to be 10.2+or-0.2 mg/100 g calculated as the reconstituted powder with an RSD of 1.8%. The LOD was determined to be 0.009, and the LOQ 0.012 mg/100 g, well below the SMPR requirements of 0.7 and 2 mg/100 g, respectively. Repeatability RSDs over the range of the assay (2-200 mg/100 g) ranged from 1.0 to 5.93%.
机译:产生了通过离子色谱法(IC)测定婴儿配方食品和成人营养品中胆碱的方法和抑制电导率的单实验室验证(SLV)数据,并提交给婴儿配方食品和成人营养品利益相关者小组(SPIFAN)专家审查专家组(ERP)在2012年9月30日至10月3日在内华达州拉斯维加斯举行的AOAC年度会议上。ERP对该数据进行了审查,并得出结论认为该数据符合建立的标准方法性能要求(SMPR)并批准该方法为AOAC官方第一个行动。应ERP的要求,对17种SPIFAN矩阵(包括强化和安慰剂产品)进行了第二次完整SLV处理。在进行IC分析之前,微波辅助酸水解可从粉末和即食(RTF)婴儿配方食品和成人营养样品中消化并释放结合的胆碱。水解后,在Thermo Scientific TM Dionex TM IonPac TM CS19色谱柱上将胆碱与普通阳离子分离,然后抑制电导检测。测量总胆碱,并以mg / 100 g复溶物质或RTF的原样形式报告为胆碱离子。在SMPR中指定的分析范围内(2-250 mg / 100 g)对系统进行了校准。加标胆碱含量为50%和100%时加标样品的回收率在93.1%至100.7%之间,对于<2 mg / 100 g的产品,RSD <= 6.7%,对于包含2-100 mg / 100 g的产品,RSD <= 4.1% 。在6天的时间间隔内确定了美国国家标准技术研究院标准参考材料1849a的准确度,发现该粉末的重新配制粉末的相对标准偏差为1.8%,计算得出的准确度为10.2+或-0.2 mg / 100 g。确定的LOD为0.009,LOQ为0.012 mg / 100 g,分别远低于SMPR要求的0.7和2 mg / 100 g。在测定范围(2-200 mg / 100 g)内,重复性RSD为1.0至5.93%。

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