Method for rapidly detecting urine sugar and uric acid in solution
A solution and urine sugar technology, applied in measuring devices, material analysis by observing the influence of chemical indicators, instruments, etc., can solve the problems of expensive instruments, troublesome transportation, etc., and achieve low cost, fast operation, and easy operation Effect
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Embodiment 1
[0040] First, the desktop printer is modified, and the hydrophobic material alkyl ketene dimer (AKD) is formulated into a solution (AKD: n-heptane = 2g: 25ml), which is added dropwise into the ink cartridge for printing. At the same time, use Word to design the detection area of the paper chip. The outline of the paper chip is printed first, followed by the hydrophobic areas. Finally, put the printed filter paper in an oven at 98°C for about 5 minutes, so that AKD is more tightly bound to the surface of the filter paper to form hydrophobic channels ( figure 1 ). The paper chip obtained by this method can be loaded with 3-5 μL of reagents, effectively ensuring that the reagents used for detection do not leak out of the detection area.
Embodiment 2
[0042] (1) Add the following reagents and sample solutions in sequence on the paper chip: glucose oxidase enzyme activity is 120U / mL, dosage 0.6μL; horseradish peroxidase enzyme activity is 80U / mL, dosage 0.6μL; concentration of potassium iodide solution 0.6mol / L, the dosage is 1.0μL; the urine glucose standard solution concentration gradient is 2.0, 4.0, 6.0, 8.0, 10.0g / L, and the glucose sample solution with a concentration of 3.0g / L is used to verify the standard curve to determine the error of the actual sample , the dosage is 1.0 μL.
[0043] (2) Load each reagent and urine sugar solution according to the above sequence, and react for about 10 minutes to fully develop the color ( figure 2 ), take pictures of the paper chip, measure the RGB color intensity values corresponding to different concentrations of urine sugar solutions with imageJ software, make a linear curve between the intensity value and the concentration of the standard solution, and draw the correlation ...
Embodiment 3
[0045] (1) Add 1.0 μL of 4mol / L 4-aminoantipyrine (4-AAP) and 1.0 μL of 8mol / L 3,5-dichloro-2-hydroxy-benzenesulfonate (DHBS) to the paper chip in sequence , Enzyme activity unit 80U / mL uric acid oxidase (UOD) 1.0μL, enzyme activity unit 339U / mL horseradish peroxidase (HRP) 1.0μL, dry the area where the reagent is to be loaded until no trace of water is visible;
[0046] (2) Add different concentrations of uric acid standard solutions and sample solutions to the paper chip detection area of the four reagents, fully react, and wait for the color to appear ( image 3 );
[0047] (3) Take a picture with a mobile phone and use imageJ software to measure the RGB color intensity of the color area, and bring it back to the standard curve to calculate the concentration of uric acid in the solution.
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