Method for detecting nitrite in blood
A nitrite and detection method technology, which is applied in the preparation of test samples, color/spectral characteristic measurement, etc., can solve the problems of lower detection sensitivity, large matrix interference, and multiple sample volumes, so as to improve detection sensitivity and detection efficiency High, the effect of overcoming the detection error
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Embodiment 1
[0021] 1. Preparation of nitrite standard working curve
[0022] ①Preparation of matrix blank solution: Take 10 mL of fresh blood without nitrite plus anticoagulant, put it into a centrifuge, centrifuge at 6000r / min for 8min, take 5 mL of the supernatant into a clean centrifuge tube, add 0.2 A protein precipitation and decolorization agent consisting of 1 mL of mol / L sodium hydroxide solution and 1 g of zinc sulfate was mixed evenly, centrifuged at 5000 r / min for 10 min, and the supernatant was taken out to obtain an almost colorless and transparent matrix blank solution.
[0023] ②Take NO with a concentration of 1.0μg / mL 2 - 20, 40, 60, 80, 100 μL standard solutions in micro test tubes, dilute to 500 μL with the matrix blank solution prepared in step ①, add 25 μL of GriessA reagent, mix well; add 25 μL of GriessB reagent after 1 min, mix well. Take 200 μL of the mixed chromogenic solution in the microplate plate, measure the absorbance at the wavelength of 490nm of the mic...
Embodiment 2
[0027] 1. make nitrite standard working curve by embodiment 1.
[0028] 2. Sample processing and measurement results
[0029] Blood test: Take 5 mL of fresh blood with anticoagulant, put it in a centrifuge and centrifuge at 8000r / min for 5 minutes, take 2 mL of supernatant, add 0.4 mL of 0.2 mol / L sodium hydroxide solution and 0.4 g of zinc sulfate The protein precipitation and decolorization agent composed, mix well, centrifuge at 6000r / min for 6min to separate, take out the supernatant, add 1mL of acetonitrile, centrifuge at 6000r / min for 5min and separate, take the supernatant into 500μL micro test tube, add 25μL of GriessA reagent, mix well ; After 1 min, add 25 μL of GriessB reagent and mix well. Take 200 μL of the mixed chromogenic solution in the microplate, measure the absorbance at the wavelength of 490 nm of the microplate reader to be 0.011, and compare the linear regression equation obtained in step (1), calculate the content of nitrite in the sample as 0.062 μg / ...
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