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采用柱切换液相色谱/脉冲安培法测定婴儿配方奶粉和成人营养食品中的肌醇(游离态及以磷脂酰肌醇形式结合的肌醇):首次行动 2011.18

Determination of myo-inositol (free and bound as phosphatidylinositol) in infant formula and adult nutritionals by liquid chromatography/pulsed amperometry with column switching: first action 2011.18.

作者信息

Schimpf Karen, Thompson Linda, Baugh Steve

机构信息

Abbott Laboratories, 3300 Stelzer Rd, Columbus, OH 43219, USA.

出版信息

J AOAC Int. 2012 Jul-Aug;95(4):937-42. doi: 10.5740/jaoacint.cs2011_18.

Abstract

Myo-inositol is a 6-carbon cyclic polyalcohol also known as meso-inositol, meat sugar, inosite, and i-inositol. It occurs in nature in both free (myo-inositol) and bound (inositol phosphates and phosphatidylinositol) forms. For the determination of free myo-inositol, samples are mixed with dilute hydrochloric acid to extract myo-inositol and precipitate proteins, diluted with water, and filtered. For the determination of myo-inositol bound as phosphatidylinositol, samples are extracted with chloroform, isolated from other fats with silica SPE cartridges, and hydrolyzed with concentrated acid to free myo-inositol. Prepared samples are first injected onto a Dionex CarboPac PA1 column, which separates myo-inositol from other late-eluting carbohydrates. After column switching, myo-inositol is further separated on a CarboPac MA1 column using a 0.12% sodium hydroxide mobile phase; strongly retained carbohydrates are eluted from the PA1 column with a 3% sodium hydroxide mobile phase. Eluant from the CarboPac MA1 analytical column passes through an electrochemical detector cell where myo-inositol is detected by pulsed amperometry using a gold electrode. The method showed appropriate performance characteristics versus selected established standard method performance requirement parameters for the determination of myo-inositol: linear response; repeatability (RSDr) of 2%; and intermediate precision (RSDir) of 2.5%. Instrument LOD and LOQ were 0.0004 and 0.0013 mg/100 mL, respectively, and correspond to a free myo-inositol quantitation limit of 0.026 mg/100 g and a phosphatidylinositol quantitation limit of 0.016 mg/100 g. Correlation with the reference microbiological assay was good. The proposed method has been accepted by the Expert Review Panel as an AOAC First Action Method, suitable for the routine determination of myo-inositol in infant formula and adult nutritionals.

摘要

肌醇是一种六碳环状多元醇,也被称为内消旋肌醇、肉糖、纤维醇和i - 肌醇。它在自然界中以游离(肌醇)和结合(肌醇磷酸酯和磷脂酰肌醇)两种形式存在。测定游离肌醇时,将样品与稀盐酸混合以提取肌醇并沉淀蛋白质,用水稀释后过滤。测定以磷脂酰肌醇形式结合的肌醇时,样品先用氯仿萃取,通过硅胶固相萃取柱与其他脂肪分离,再用浓酸水解以释放出游离肌醇。制备好的样品首先注入戴安CarboPac PA1柱,该柱可将肌醇与其他较晚洗脱的碳水化合物分离。柱切换后,肌醇在CarboPac MA1柱上使用0.12%氢氧化钠流动相进一步分离;强保留的碳水化合物用3%氢氧化钠流动相从PA1柱上洗脱。来自CarboPac MA1分析柱的洗脱液通过电化学检测池,在该池中使用金电极通过脉冲安培法检测肌醇。与选定的已确立的肌醇测定标准方法性能要求参数相比,该方法显示出适当的性能特征:线性响应;重复性(RSDr)为2%;中间精密度(RSDir)为2.5%。仪器检测限和定量限分别为0.0004和0.0013 mg/100 mL,分别对应游离肌醇定量限为0.026 mg/100 g和磷脂酰肌醇定量限为0.016 mg/100 g。与参考微生物测定法的相关性良好。该方法已被专家评审小组认可为AOAC首次行动方法,适用于婴儿配方奶粉和成人营养产品中肌醇的常规测定。

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