scholarly journals Radioimmunoassay of bound and free melatonin in plasma

1998 ◽  
Vol 44 (2) ◽  
pp. 304-310 ◽  
Author(s):  
Wei-Li Di ◽  
Aban Kadva ◽  
Ovrang Djahanbakhch ◽  
Robert Silman

Abstract We describe a nonextraction procedure, and two extraction procedures, for RIA of melatonin in human plasma. All procedures showed a diurnal rhythm of melatonin in human subjects, with interindividual differences greater than interprocedure differences. However, further investigations demonstrated considerable variability of recovery in the nonextraction procedure, suggesting a variability of binding proteins between samples. Combining recovery and dialysis experiments in the extraction procedures, we demonstrated that chloroform was unable to extract albumin-bound melatonin from a human serum albumin solution but, paradoxically, was able to extract bound and free melatonin from a plasma sample. The methanol extraction procedure extracted free and bound melatonin from all sources. These results indicate that albumin binding can substantially affect the RIA procedures. We conclude that assays should be validated against free and bound melatonin and that the two forms should be independently investigated when assessing bioactivity.

1975 ◽  
Vol 21 (11) ◽  
pp. 1638-1643 ◽  
Author(s):  
Susan B McCluskey ◽  
G N B Storey ◽  
G K Brown ◽  
D G More ◽  
W J O’Sullivan

Abstract We report a fluorometric technique for determination of albumin-titratable bilirubin in the jaundiced neonate. Although bilirubin alone has very little native fluorescence, considerable emission is observed in the presence of albumin under acid conditions. Analysis of the plasma sample alone and in the presence of excess human serum albumin solution appears to reflect the bilirubin tightly bound to albumin and the total serum bilirubin, respectively. The difference between these two values has been designated as "albumin-titratable bilirubin." Where the concentration of albumin-titratable bilirubin is considerable, a typical saturation effect is observed. In samples where the circulating bilirubin is strongly bound to endogenous albumin, no change in fluorescence is seen when exogenous albumin is added. Results correlate well with the clinical picture


Polyhedron ◽  
1999 ◽  
Vol 18 (5) ◽  
pp. 695-697 ◽  
Author(s):  
Xinyu Li ◽  
Xiaojing Li ◽  
Shanrong Zhang ◽  
Fengkui Pei

1956 ◽  
Vol 185 (1) ◽  
pp. 54-60 ◽  
Author(s):  
Ulrich Westphal ◽  
Hilliard E. Firschein ◽  
Eli M. Pearce

Interaction between low concentrations of cortisol-4-C14 or progesterone-4-C14 and serum proteins was investigated by paper-electrophoretic methods in human serum albumin solution as well as in human and rat serum. Between 2 and 10% of cortisol and between 70 and 90% of progesterone were found to be bound and thus transported by human albumin. Similar transport values were observed in paper-chromatographic studies in which the steroids migrated in aqueous solution, in the presence and absence of serum proteins. A critical evaluation was made on the use of paper-electrophoretic procedures in protein-binding studies. The demonstration of a firm albumin binding of progesterone, and a comparatively loose attachment of cortisol, is in general agreement with results obtained by ultracentrifugation and ‘free’ electrophoresis. Some physiological implications are mentioned.


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