Production and certification of four frozen human serum certified reference materials containing creatinine and electrolytes

被引:19
作者
Barbagallo, Romina P. [1 ]
Boley, Nick [1 ]
Holcombe, Gill [1 ]
Merson, Sheila [1 ]
Mussell, Chris [1 ]
Pritchard, Caroline [1 ]
Stokes, Peter [1 ]
Wood, Steve [1 ]
Ducroq, David [2 ]
Thomas, Annette [2 ]
机构
[1] LGC Ltd, Res & Technol Div, Teddington TW11 0LY, Middx, England
[2] WEQAS, Reference Lab, Cardiff CF14 5WF, Wales
关键词
D O I
10.1258/acb.2007.007126
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: This paper describes the preparation, analysis and certification of four frozen human serum certified reference materials (CRMs) containing creatinine and the electrolytes calcium, lithium, magnesium, potassium and sodium. These materials have been prepared to give concentrations of these analytes that cover the currently accepted analytical range. Methods: The analysis of the materials for certification purposes has been carried out using methodology traceable to primary standards, and which is acceptable as a reference method. The certification methods include liquid chromatography-mass spectrometry (LC-MS) with exact-matching isotope dilution calibration (EM-IDMS) for creatinine, inductively-coupled plasma optical emission spectroscopy (ICP-OES), ICP-MS and isotope-dilution incluctively-coupled plasma mass spectroscopy (ID-ICP-MS) for the electrolytes. Results: The uncertainties estimated for these certified values include a component from the characterization measurements, as well as contributions from possible inhomogeneity and long-term instability. The certified values have been corroborated by measurements obtained in a major UK External Quality Assessment scheme, which have, with the exception of the determination of creatinine at a particularly low concentration, given excellent agreement. Conclusions: The materials are intended for use by pathology laboratories and manufacturers of in vitro diagnostic (IVD) kits for validation of existing routine methodology to a traceable standard, which will promote harmonization between the different methods, instruments and IVD kits used in these laboratories.
引用
收藏
页码:160 / 166
页数:7
相关论文
共 22 条
  • [1] PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE
    COCKCROFT, DW
    GAULT, MH
    [J]. NEPHRON, 1976, 16 (01) : 31 - 41
  • [2] K/DOQI clinical practice guidelines for chronic kidney disease: Evaluation, classification, and stratification - Foreword
    Eknoyan, G
    Levin, NW
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2002, 39 (02) : S14 - S266
  • [3] EVENSON MA, 2001, TIETZ FUNDAMENTALS C, P56
  • [4] FAIRFIELDSMITH H, 1936, J COUNC SCI IND RES, V9, P110
  • [5] Jaffe M., 1886, PHYSIOL CHEM PHYS M, V10, P391, DOI DOI 10.1515/BCHM1.1886.10.5.391
  • [6] CREATININE ASSAY BY A REACTION-KINETIC PRINCIPLE
    LARSEN, K
    [J]. CLINICA CHIMICA ACTA, 1972, 41 (01) : 209 - &
  • [7] A more accurate method to estimate glomerular filtration rate from serum creatinine: A new prediction equation
    Levey, AS
    Bosch, JP
    Lewis, JB
    Greene, T
    Rogers, N
    Roth, D
    [J]. ANNALS OF INTERNAL MEDICINE, 1999, 130 (06) : 461 - +
  • [8] Recommendations for improving serum creatinine measurement: A report from the laboratory working group of the National Kidney Disease Education Program
    Myers, GL
    Miller, WG
    Coresh, J
    Fleming, J
    Greenberg, N
    Greene, T
    Hostetter, T
    Levey, AS
    Panteghini, M
    Welch, M
    Eckfeldt, JH
    [J]. CLINICAL CHEMISTRY, 2006, 52 (01) : 5 - 18
  • [9] *NAT COMM CLIN LAB, 1998, EP14 NCCLS
  • [10] OSBERG IM, 1978, CLIN CHEM, V24, P1196