Melatonin in Human Serum—A Collaborative Study of Current Radioimmunoassays

Author(s):  
L. Wetterberg ◽  
O. Eriksson
1985 ◽  
Vol 13 (3) ◽  
pp. 185-197 ◽  
Author(s):  
Claude Vincent ◽  
Jacques Esteve ◽  
Edward H. Cooper ◽  
Ingrid Deconninck ◽  
Mary Forbes ◽  
...  

Bioanalysis ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 265-276
Author(s):  
Noritaka Hashii ◽  
Yoshiko Tousaka ◽  
Koji Arai ◽  
Yoshimasa Enoki ◽  
Suguru Fukuda ◽  
...  

Aim: We aimed to develop an easy, low-cost and versatile mass spectrometric method for the bioanalysis of a therapeutic monoclonal antibody (mAb) in human serum that employs peptide adsorption-controlled (PAC)-LC/MS using selected reaction monitoring mode (LC–MS/MS-SRM). Materials & methods: Rituximab was used as a model mAb. To apply the method to human serum samples, a peptide of the complementarity-determining region was selected as the surrogate peptide. The usefulness of PAC-LC–MS/MS-SRM was evaluated by a collaborative study. Results: The calibration curve ranged from 0.5 (or 1.0) to 1000.0 μg/ml. The selectivity, linearity, accuracy and precision met the predefined acceptance criteria. Conclusion: Our method could be a useful bioanalytical method for the quantification of mAbs in clinical samples.


1974 ◽  
Vol 19 (3) ◽  
pp. 113-118 ◽  
Author(s):  
Anne Ferguson ◽  
Heather M. Dick ◽  
R. J. Fallon ◽  
R. W. Logan ◽  
Carolyn M. Meudell

In a collaborative study involving four hospital laboratories Immunoglobulins G, A and M were assayed in 12 human serum specimens. The aims were to define the magnitude of inter-laboratory discrepancies in the values obtained, to identify likely reasons for these discrepancies, and to ascertain whether they were reduced when Immunoglobulins were assayed by comparison with a British Standard preparation. The results of this experiment emphasise the importance of continuing experience in Immunoglobulin assay techniques; there may be considerable variation in the results obtained when the same specimen is tested in different laboratories, or at different times in one laboratory; these discrepancies are reduced if laboratories use reagents from the same source (commercial sources in this case). When the usual laboratory Immunoglobulin standards were replaced by a British Standard preparation, there was no improvement in the results for IgG and IgA assays, but inter-laboratory variation in IgM measurements was significantly reduced.


2015 ◽  
Vol 48 (06) ◽  
Author(s):  
C Rothammer ◽  
E Haen
Keyword(s):  

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