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Clinical Chemistry, Vol 21, 1932-1934, Copyright © 1975 by the American Association for Clinical Chemistry
1 Division of Clinical Chemistry, Babies Hospital, The Childrens
Medical and Surgical Center of New York at Columbia Presbyterian Medical Center; and The Department of Pediatrics, College of
Physicians and Surgeons of Columbia University, 3959 Broadway,
New York, N. Y. 10032.
In this method, blood is collected in ammonium heparinized microhematocrit tubes and lactate is directly determined in the plasma, separated within 15 min from the erythrocytes. Lactate is assayed by mixing 10 µl of sample with NAD+ and lactate dehydrogenase in tris(hydroxymethyl)aminomethane hydrazine buffer. The rate of increase in absorbance of the NADH formed, measured at 340 nm, is proportional to lactate concentration. The assay is complete in 4 min and absorbance is linearly related to concentration from 0.625 to 15 mmol/ liter. Analytical recoveries of lactate added to plasma averaged 104% (range, 91-116%). Results compared well for plasma samples analyzed by this method with the CentrifiChem and the Du Pont aca.
Submitted on August 6, 1975
The following articles in journals at HighWire Press have cited this article:
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H. G. Pietersen, C. J. M. Langenberg, G. Geskes, A. Kester, S. d. Lange, G. J. Van der Vusse, A. J. M. Wagenmakers, and P. B. Soeters MYOCARDIAL SUBSTRATE UPTAKE AND OXIDATION DURING AND AFTER ROUTINECARDIAC SURGERY J. Thorac. Cardiovasc. Surg., July 1, 1999; 118(1): 71 - 81. [Abstract] [Full Text] [PDF] |
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