Stable liquid urobilinogen control composition

Chemistry: analytical and immunological testing – Composition for standardization – calibration – simulation,...

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436 12, 514422, G01N 3700

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058664246

ABSTRACT:
The present invention addresses the need to ensure that clinical tests for urobilinogen in urine are properly working. The invention specifically provides a novel liquid urobilinogen composition which remains stable in liquid form for eighteen months and a method for making the same.

REFERENCES:
Kotal et al., Clinica Chemica Acta, 202, pp. 1-10, Oct. 1991.
Fetter et al., American Journal of Medical Technology 47(9), Sep. 1981.
Rupe et al., Clinical Chemistry 27(8), pp. 1385-1387, Aug. 1981.
Fischer et al., Hoppe-Seyler's Zeitschrift F. Physiol. Chemie CXXVII pp. 293-316 (translation), 1924.
Watson et al, Biochemical Medicine 2, 484-508, 1969.
Petryka "Variations in Hydrogenation of Bile Pigments . . . ", Annals New York Acaemy of Sciences, 206, pp. 701-710 (1973) Translation of JP62175666 (Hisatsu et al.).
Gray et al. "The Chemistry of the Bile Pigments . . . " J.Chem. Soc. 2268 (1961) pp. 2268-2285.
Levy et al. "Renal Excretion of Urobilinogen in the Dot", CA Abstract 69:104478 of J. Clin. Invest. (1968) pp. 2117-2124 (47(9) (1968).
Fetter et al., Biochemical Medicine, pp. 484-508, 1969.

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