A sensitive, direct colorimetric assay of serum iron using the chromogen, nitro-PAPS
1988
Abstract A direct colorimetric method is presented for the determination of serum iron in 0.1-ml sized samples, using a new, water-soluble, reagent, 2-(5-Nitro-2-pyridylazo)-5-( N -propyl- N -sulfopropylamino)phenol Na salt ( ϵ 585nm = 9.4 × 10 4 l/mol per cm). Interference of copper and zinc in sera can be eliminated entirely by forming copper- and zinc-thioglycollate complexes immediately upon the dissociation of the protein-bound iron, copper and zinc by thioglycollate and sodium dodecyl sulfate. The serum blank was minimized by the use of sodium dodecyl sulfate as a protein denaturant. Within-run and between-run precision (CV) were in the range of 0.7–2.9% and 1.1–3.6%, respectively, depending on the serum iron content. A good correlation ( r = 0.995) was obtained between this method and the reference method proposed by the International Committee for Standardization in Hematology.
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