Development of a new standard reference material: SRM 1955 (homocysteine and folate in human serum)

被引:43
作者
Satterfield, Mary B.
Sniegoski, Lorna T.
Sharpless, Katherine E.
Welch, Michael J.
Hornikova, Adriana
Zhang, Nien-Fan
Pfeiffer, Christine M.
Fazili, Zia
Zhang, Mindy
Nelson, Bryant C. [1 ]
机构
[1] NIST, Analyt Chem Div, Gaithersburg, MD 20899 USA
[2] NIST, Stat Engn Div, Gaithersburg, MD 20899 USA
[3] Ctr Dis Control & Prevent, Div Lab Sci, Atlanta, GA 30341 USA
关键词
isotope dilution mass spectrometry; standard reference material; homocysteine; folate; 5-methyltetrahydrofolic acid; 5-formyltetrahydrofolic acid; folic acid;
D O I
10.1007/s00216-006-0434-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Total homocysteine (tHCY) and folate are interrelated biomarkers for arteriosclerosis and coronary heart disease. Although many different methods for both tHCY and folate are clinically available, the intermethod and interlaboratory results are often poor, resulting in the need for a matrix reference material and reference methods. The National Institute of Standards and Technology (NIST) has developed isotope dilution liquid chromatography/mass spectrometry (LC/MS) and liquid chromatography/ tandem mass spectrometry (LC/MS/MS) methods for determination of tHCY and several folate forms including 5-methyltetrahydrofolic acid (5MT) and folic acid (FA). Additionally, a method for simultaneous measurement of tHCY, 5MT, and FA has been developed and validated. In collaboration with the Centers for Disease Control and Prevention (CDC), mass spectrometric methods and methods used in clinical laboratories have been applied to characterize a new Standard Reference Material (SRM), SRM 1955, "Homocysteine and Folate in Human Serum," containing low, medium, and high levels of tHCY and 5MT. Additionally, FA, 5-formyltetrahydrofolic acid (5FT), vitamin B-12, and total folate values are provided. Use of the new SRM should improve clinical measurements and will permit traceability to internationally recognized certified reference materials, as described by European Directive 98/79/EC on in vitro diagnostic medical devices.
引用
收藏
页码:612 / 622
页数:11
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