A rapid and reliable method for measuring serum albumin employing brom
cresol green is described. The addition of albumin to a solution of br
omcresol green in a 0.075 M succinate buffer pH 4.20 results in an inc
rease in absorbance at 628 nm. The absorbance-concentration relationsh
ip is linear for samples containing up to 6 g/dl albumin. Bilirubin, m
oderate lipemia, and salicylate do not interfere with the analysis. Th
e use of a nonionic surfactant (Brij-35) reduces the absorbance of the
blank, prevents turbidity and provides linearity. The results by this
method agree very well with those obtained by electrophoresis and sal
t fractionation. The method is simple, it has excellent precision and
the reagents are stable. A protein standard is introduced which can be
employed for both the total serum proteins and albumin determinations
.