Campos-Giménez Esther, Fontannaz Patric, Redeuil Karine, Kilinc Tamara, Dowell Dawn
Nestlé Research Center, Nestec Ltd, Department of Quality Assurance, Vers-Chez-les-Blanc, 1000 Lausanne 26, Switzerland.
J AOAC Int. 2013 Sep-Oct;96(5):1065-7. doi: 10.5740/jaoacint.13-141.
During the AOAC Annual Meeting held in Las Vegas, NV from September 30 to October 3, 2012, the Stakeholder Panel on Infant Formula and Adult Nutritionals convened to review single-laboratory validation data submitted for the method, Vitamin C in Adult/Pediatric Formula by Ultra-Performance Liquid Chromatography with Ultraviolet Detection. This method is a modified version of the method "HPLC-UV Determination of Total Vitamin C in a Wide Range of Fortified Food Products" previously published in Food Chem., 94, 626-631 (2006). The SLV data from the modified method were reviewed and compared to the standard method performance requirements (SMPR 2012.012), and it was concluded that the method meets the requirements. The method was approved as AOAC Official First Action. The method is based on the acidic extraction of ascorbic acid in the presence of Tris[2-carboxyethyl] phosphine (TCEP) as a reducing agent. Separation was achieved on a C18 column with a sodium acetate eluent (pH 5.4) combined with TCEP and decylamine as an ion-pairing agent. Accuracy rates were between 90 and 100%. Repeatability RSD (RSD,) ranged from 1.4 to 2.5%, and intermediate reproducibility RSD (RSDiR) ranged from 1.3 to 7.5%.
在2012年9月30日至10月3日于内华达州拉斯维加斯举行的美国官方分析化学师协会(AOAC)年会上,婴儿配方奶粉和成人营养产品利益相关者小组召开会议,审查提交的“采用超高效液相色谱-紫外检测法测定成人/儿童配方奶粉中的维生素C”方法的单实验室验证数据。该方法是先前发表于《食品化学》94卷626 - 631页(2006年)的“高效液相色谱-紫外检测法测定多种强化食品中的总维生素C”方法的改进版本。对改进方法的单实验室验证数据进行了审查,并与标准方法性能要求(SMPR 2012.012)进行了比较,得出该方法符合要求的结论。该方法被批准为AOAC官方首次行动方法。该方法基于在三[2-羧乙基]膦(TCEP)作为还原剂的存在下,对抗坏血酸进行酸性萃取。在C18柱上,使用乙酸钠洗脱液(pH 5.4),并结合TCEP和癸胺作为离子对试剂实现分离。准确率在90%至100%之间。重复性相对标准偏差(RSDr)范围为1.4%至2.5%,中间精密度相对标准偏差(RSDIR)范围为1.3%至7.5%。