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Measurement of Ceruloplasmin from Its Oxidase Activity in Serum by Use of o-Dianisidine Dihydrochloride

Clinical Chemistry · 1974 · Vol. 20(12) · pp. 1556–1563
Karl SchosinskyHarold P. LehmannMyrton F. Beeler

Abstract

Abstract We have developed a new method for determination of serum ceruloplasmin from its oxidase activity, in which o-dianisidine dihydrochloride is used as substrate. o-Dianisidine dihydrochloride is more stable than is the more widely used p-phenylenediamine substrate, and forms a stable product that is measured at 540 nm. Correlation was good between results of this method and those obtained with both a p-phenylenediamine substrate method (r = 0.98) and a radial immunodiffusion procedure (r = 0.97). There is little or no interference from reducing or colored components of serum. The coefficient of variation (day-to-day) for the method was 4.2%. A normal range of 62-140 U/ liter has been determined by the reported method.

Trace Elements in HealthCeruloplasminRadial immunodiffusionChemistrySubstrate (aquarium)ChromatographyOxidase testCoefficient of variationEnzymeBiochemistryMedicine

MeSH terms

Analysis of VarianceAniline CompoundsAnisolesBilirubinBiphenyl CompoundsCeruloplasminCitratesCopperFemaleImmunodiffusionHemoglobinsHumansHydrogen-Ion ConcentrationHyperlipidemiasIndicators and Reagents

Funding

  • U.S. Public Health Service
Citations
593
FWCI
1.99
field-weighted impact
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10
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86%
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References
The Determination of Enzyme Dissociation Constants
Journal of the American Chemical Society · 1934 · 12,048 citations
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