化学
重复性
分析物
色谱法
抗坏血酸
维生素
产量(工程)
动力学
米氏-门汀动力学
基质(化学分析)
酶
生物化学
食品科学
酶分析
物理
量子力学
冶金
材料科学
作者
Stephanie Kobany,Dana Schmieg,David W. Plank,Lisa A Povolny,Marilyn Shepard,May M.L. Lam,Noe Galvan,Dana Brown
标识
DOI:10.5740/jaoacint.18-0317
摘要
Background: Recent development of LC methods for the determination of total folates (vitamin B9) in complex matrixes have been hindered by vitamer interconversion and yield variability. The official microbiological method (AOAC Official Methods of Analysis 944.12 and 960.46) uses an end point turbidity reading to determine folate concentration. However, when measuring complex matrixes, shifts are observed in the growth curves of the microorganism and inaccuracies are introduced to this quantification method. Objective/Methods: In addition to the tri-enzyme digestion of the standard microbiological method, we have applied enzyme modeling of the initial velocity of bacterial growth using Michaelis-Menten kinetics to achieve more accurate and reproducible determinations of total folates. Results/Conclusions: Accuracy determined through spike recovery in Infant/Adult Nutritional Drink and a complex vitamin matrix gave values acceptable to AOAC standards of 85-110%. Repeatability of the low mass fraction analyte measured at micrograms per 100 g yielded relative standard deviations <15% for all matrixes tested, including three standard reference materials.
科研通智能强力驱动
Strongly Powered by AbleSci AI