Fixed-time digital counting system for reaction rate methods

1970 ◽  
Vol 42 (9) ◽  
pp. 1055-1060 ◽  
Author(s):  
James D. Ingle ◽  
Stanley R. Crouch
Author(s):  
Hironari Takehara ◽  
Yuta Nakamoto ◽  
Kiyotaka Sasagawa ◽  
Hiroaki Takehara ◽  
Toshihiko Noda ◽  
...  

1982 ◽  
Vol 54 (4) ◽  
pp. 755-761 ◽  
Author(s):  
F. J. Holler ◽  
R. K. Calhoun ◽  
S. F. McClanahan

2000 ◽  
Vol 43 (4) ◽  
pp. 353-354
Author(s):  
Yu. B. Kolyada ◽  
V. N. Yanushkin

1979 ◽  
Vol 25 (4) ◽  
pp. 611-613 ◽  
Author(s):  
P K Li ◽  
B C Shull

Abstract We describe a fixed-time, enzymatic, reaction-rate procedure for determining plasma ammonia with a centrifugal analyzer (Rotochem IIA/36; American Instrument Co., silver Spring, MD 20910), with NADPH as cofactor. The reaction is based on that of da Fonseca-Wollheim's modification [J. Clin. Chem. Clin. Biochem. 11, 421 (1973)] of the Kirstein reaction, which depends on the catalytic amination of alpha-ketoglutarate by the action of glutamate dehydrogenase with NADPH as the cofactor instead of NADH. Use of NADPH minimizes interference from endogenous reactions such as that between lactate dehydrogenase and pyruvate. This method permits shortened preincubation time and thus improves both specificity and precision. This assay requires 100 microliter of freshly collected heparinized plasma, gives quantitative analytical recovery, and the standard curve is linear to 430 mumol/L. Data are presented comparing results with those by two other enzymatic ammonia procedures.


1980 ◽  
Vol 26 (12) ◽  
pp. 1713-1717 ◽  
Author(s):  
P K Li ◽  
J T Lee ◽  
M H MacGillivray ◽  
P A Schaefer ◽  
J H Siegel

Abstract In the course of studying the control of blood glucose in juvenile onset diabetics, we developed convenient methods for determining beta-hydroxybutyrate and acetoacetate. Here we describe fixed-time, enzymic, reaction-rate procedures for directly measuring these organic acids with a centrifugal analyzer (Rotochem IIA/36) or a computer-backed spectrophotometer (Gilford 102 system). In either case, the method requires only 20 micro L of plasma; is rapid, accurate, and precise; and analytical recovery is quantitative. Data are presented comparing results obtained with both instruments. Metabolic acidosis can be rapidly assessed and monitored with these methods, as illustrated by an example.


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