International Standard for serum vitamin B12 and serum folate: international collaborative study to evaluate a batch of lyophilised serum for B12 and folate content

Author(s):  
Susan J. Thorpe ◽  
Alan Heath ◽  
Sheena Blackmore ◽  
Anne Lee ◽  
Malcolm Hamilton ◽  
...  
2016 ◽  
Vol 54 (9) ◽  
pp. 1467-1472 ◽  
Author(s):  
Susan J. Thorpe ◽  
Peter Rigsby ◽  
Graham Roberts ◽  
Anne Lee ◽  
Malcolm Hamilton ◽  
...  

AbstractBackground:Investigation of possible B12 and folate deficiencies requires measurement of these vitamins in serum. There is evidence that holotranscobalamin (holoTC), the active portion of B12 available to cells, is a more specific marker of early B12 deficiency than total B12. The availability of immunoassays for holoTC prompted an international collaborative study to assign a holoTC value to the World Health Organization (WHO) 1st International Standard (IS) for vitamin B12 and serum folate, 03/178.Methods:The IS, 03/178, and three serum samples with different holoTC levels were assayed by 12 laboratories in eight countries using manual and automated immunoassays for holoTC; one laboratory additionally performed an in-house assay. Fourteen sets of data were analysed.Results:Overall, the IS, 03/178, and the three serum samples demonstrated assay linearity and parallelism. An overall geometric mean (GM) holoTC value of 106.8 pmol/L was obtained for 03/178, with an inter-laboratory geometric coefficient of variation (GCV) of 10.5%. There was a reduction in inter-laboratory variability when the holoTC levels in the serum samples were determined relative to the IS with an assigned holoTC value rather than to the assays’ calibration. Accelerated degradation studies showed that 03/178 was sufficiently stable to serve as an IS for holoTC.Conclusions:The WHO Expert Committee on Biological Standardization endorsed the proposal to assign a holoTC value of 107 pmol/L to 03/178, corresponding to 0.107 pmol per ampoule, for use as the 1st IS for vitamin B12, serum folate, and holoTC.


1984 ◽  
Vol 52 (02) ◽  
pp. 148-153 ◽  
Author(s):  
D P Thomas ◽  
A D Curtis ◽  
T W Barrowcliffe

SummaryAn international collaborative study, in which 22 laboratories participated, was carried out to establish a replacement for the International Standard for Heparin. A total of 248 assays were analyzed, including APTT, thrombin inhibition and anti-Xa assays, as well as pharmacopoeial assays. Overall, there was less than 5% difference in the mean potency estimates of the candidate preparations, by all assay methods. The freeze-dried preparation 82/502 demonstrated the closest parallelism by bioassay to the existing standard and was established by WHO as the 4th International Standard for Heparin, with an assigned unitage of 1780 i.u. per ampoule.


Vox Sanguinis ◽  
2019 ◽  
Vol 114 (7) ◽  
pp. 740-748 ◽  
Author(s):  
Bernard Fox ◽  
Giles Sharp ◽  
Eleanor Atkinson ◽  
Graham Roberts ◽  
Peter Rigsby ◽  
...  

1997 ◽  
Vol 43 (9) ◽  
pp. 1582-1587 ◽  
Author(s):  
Susan J Thorpe ◽  
Dawn Walker ◽  
Paolo Arosio ◽  
Alan Heath ◽  
James D Cook ◽  
...  

Abstract A recombinant L ferritin preparation, lyophilized in ampoules and designated 94/572, was evaluated by 18 laboratories in 9 countries for its suitability as an International Standard (IS). The preparation was assayed in a wide range of in-house and commercial immunoassays against the 2nd IS for ferritin (of spleen origin; 80/578). The immunological reactivity of the recombinant material was similar to that of the 2nd IS for ferritin in the majority of assays and demonstrated adequate stability in accelerated degradation studies. On the basis of the results presented here, the WHO Expert Committee on Biological Standardization established 94/572 as the 3rd IS for ferritin, recombinant.


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