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A simple, sensitive and accurate procedure for quantitating plasma fibronectin is described. The method involves the heat denaturation of the plasma protein with high urea (8 M), chromatography on Sepharose 4B (fractionated and unfractionated) and subsequent assay by hemagglutination and/or by a specific peroxidase-linked assay. The antiserum to plasma fibronectin used in the assays does not interfere with the heat denaturation of the plasma protein. Therefore, the assay detects both the unmodified plasma fibronectin and the polymeric form of the protein. In the peroxidase-linked assay, it is less than 0.5% of the plasma proteins that interfere with the assay. The accuracy and precision of the assay are similar to that reported for previously available immunoassays. Using the peroxidase-linked assay, plasma fibronectin and fibronectin in serum were measured in normal subjects, patients with fibrotic liver disease, alcoholic hepatitis, sepsis and malignancy. Plasma fibronectin was similar in normal subjects and in patients with liver disease. In sepsis and in malignancy, plasma fibronectin was significantly elevated. In cancer patients, plasma fibronectin correlated with the level of fibronectin in the ascitic fluid.S. 361, 111 S.Ct. 1877, 114 L.Ed.2d 404 (1991). The court held that even assuming arguendo that these claims are viable they would still be time-barred because they could have been raised before the administrative agencies.
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