Determination of Vitamin B12 in Infant Formula and Adult Nutritionals by Surface Plasmon Resonance: First Action 2011.16 (Test Kit Method)

被引:5
|
作者
Vyas, Pathik [1 ]
O'Kane, Anthony A. [2 ]
Dowell, Dawn [3 ]
机构
[1] AsureQual Auckland Lab, Auckland, New Zealand
[2] Queens Univ Belfast, IAFLU, Belfast BT8 4AG, Antrim, North Ireland
[3] AOAC INT, Gaithersburg, MD 20877 USA
关键词
D O I
10.5740/jaoacint.CS2011_16
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
At the "Standards Development and International Harmonization: AOAC INTERNATIONAL Mid-Year Meeting" on June 29, 2011, an Expert Review Panel (ERP) agreed to further examine AOAC Official Method(SM) 2011.01, "Determination of Vitamin B-12 by Surface Plasmon Resonance," for use with infant formula and adult nutritionals. The original collaborative study was conducted using the Biacore Q (TM) biosensor instrument and the Biacore Q (TM) Qflex (TM) Kit Vitamin B-12 PI. Samples included in the study were infant formula, cereals, premixes, vitamin tablets, dietary supplements, and baby food. Eleven laboratories participated in the collaborative study. The results demonstrated a repeatability RSD (RSDr) of 1.59-27.8 and HorRat values for reproducibility of 0.34-1.89 in samples with levels ranging from ppm to ppb. The assay studied is a label-free protein binding-based assay that uses the principle of surface plasmon resonance to measure the interaction between vitamin B-12 and a specific binding protein by passing a portion of the prepared sample extract combined with binding protein solution across a functionalized sensor chip. The response from the functionalized sensor chip is given as free-binding protein, as the mixture binds to the prepared surface of the chip. The ready-to-use Qflex Kit Vitamin B-12 PI provides the reagents and accessories necessary to perform this assay. AOAC Method 2011.01 was approved by the AOAC Method Committee on Food Nutrition for Official First Action status, applicable to a wide range of food products, dietary supplements, and multivitamin premixes. After evaluation of the validation data available, an ERP agreed in June 2011 that the method meets standard method performance requirements, as articulated by the Stakeholder Panel on Infant Formula and Adult Nutritionals. The ERP granted the method First Action status, applicable to infant formula and adult/pediatric nutritional formula.
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页码:329 / 334
页数:6
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