Whole blood assay
A technology for whole blood samples and measured values, applied in the field of whole blood detection, can solve the problems of increasing the complexity of system design and increasing costs
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[0053] A known volume (eg, 2.0 ml) of reagent containing buffer and a mixture of enzyme and reactants for the enzyme-linked reaction (shown below) is added to the reaction cuvette.
[0054]
[0055]
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[0057] The mixture was added to a photometer and excited at 510 nm. Blank transmittance readings were taken at <1 second intervals for approximately 5 seconds.
[0058] Then, at t 0 At time points, a fixed volume (5 μL) of blood, whose plasma cholesterol level is known, is added to the cuvette and mixed. The transmittance was measured at 510 nm when the mixing was complete and the reaction time was measured for 3 minutes. The time taken to create mixing and stop the vortex in the liquid means the transmittance recorded after the 10th second from the addition of the blood sample.
[0059] Table 1 below lists examples of blank and blood transmittance signals and reference readings.
[0060] Table 1
[0061] reading time
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