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Clinical Chemistry, Vol 18, 1323-1325, Copyright © 1972 by the American Association for Clinical Chemistry
1 Departments of Medicine, Biochemistry, and Pathology, University of North Carolina, Chapel Hill, N.C. 27514;
and the Department of Pathology, University of Florida,
Gainesville, Fla. 32601.
We developed a kinetic procedure for determination of amylase activity in serum by use of nephelometric measurements. Light scattering from the substrate, a stable suspension of starch, is decreased as amylase hydrolyzes the starch to soluble fragments. Values obtained for serum amylase correlate closely with those determined by a method in which a starch-dye complex is used. Precision of the new procedure is 3.4% (relative standard deviation). Units of amylase activity can either be expressed in terms of milligrams of starch consumed or converted to more conventional amylase units.
Submitted on May 30, 1972
Accepted on July 17, 1972
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