Development and validation of control materials for the measurement of vitamin D3 in selected US foods

被引:31
作者
Phillips, Katherine M. [1 ]
Byrdwell, W. Craig [2 ]
Exler, Jacob [3 ]
Harnly, James M. [2 ]
Holden, Joanne M. [3 ]
Holick, Michael F. [4 ]
Hollis, Bruce W. [5 ]
Horst, Ronald L. [6 ]
Lemar, Linda E. [3 ]
Patterson, Kristine Y. [3 ]
Tarrago-Trani, Maria Teresa [1 ]
Wolf, Wayne R. [2 ]
机构
[1] Virginia Polytech Inst & State Univ, Dept Biochem 0308, Blacksburg, VA 24061 USA
[2] USDA, Beltsville Human Nutr Res Ctr, Food Composit & Methods Dev Lab, Beltsville, MD 20705 USA
[3] USDA, Beltsville Human Nutr Res Ctr, Nutrient Data Lab, Beltsville, MD 20705 USA
[4] Boston Univ, Sch Med, Boston, MA 02118 USA
[5] Med Univ S Carolina, Charleston, SC 29425 USA
[6] Heartland Assays Inc, Ames, IA 50010 USA
关键词
vitamin D; cholecalciferol; ergocalciferol; control materials; reference values; analytical methods; analysis; cereal; milk; cheese; fish; orange juice; interlaboratory variability;
D O I
10.1016/j.jfca.2008.05.003
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
As part of the United States Department of Agriculture's (USDA) National Food and Nutrient Analysis Program (NFNAP), food composition data for vitamin D in the USDA National Nutrient Database for Standard Reference are being updated and expanded, focusing on high priority foods and validated analytical methodology. A lack of certified reference materials and analytical methods validated for these key foods required the development of five matrix-specific control composite materials (CC) (canned salmon and vitamin D-3 fortified cereal, orange juice, milk, and cheese). Each of six experienced laboratories (research and commercial) analyzed vitamin D-3 in five subsamples of each CC in five separate analytical batches, with one subsample of each material in each run. Research laboratories performed recovery studies, mass spectrometric analysis, and other studies to validate quantitation in each matrix. Initial results showed a wide disparity between the six laboratories (RSDs of 26-46%). Extensive collaboration resolved several problems related to calibration standards, extraction solvents and the internal standard, achieving final values with RSDs of approximately 10%, validated by mass spectrometry tests that confirmed lack of matrix interferences in these foods. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:527 / 534
页数:8
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