Urine sulfhydryl compound mercury-free detection test strip and preparation method
A mercapto compound, detection test paper technology, applied in the direction of analysis by chemical reaction of materials, material analysis by observing the impact on chemical indicators, etc. The detection rate is accelerated, the use safety is improved, and the operability is strong.
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Embodiment 1
[0024] 1) Prepare buffer solution: Weigh 1.5g sodium dihydrogen phosphate and 70.22g disodium hydrogen phosphate dodecahydrate, add water to make the volume to 1L, and the pH value of the buffer solution is 7.8.
[0025] 2) Weigh 6.14g of 5,5'-dithiobis(2-nitrobenzoic acid) (DNTB) (6.14g / L), 0.32g of disodium ethylenediaminetetraacetic acid (EDTA) (320mg / L L), 10g of 2-methyl-2,4-pentanediol (15g / L), 10g of silicotungstic acid (10g / L), 14g of polyethylene glycol and 1.7g of Triton X-100, the above group Partially added to the prepared buffer;
[0026] 3) After the components prepared in step 2) are completely dissolved, soak the filter paper in the solution, take it out and dry it, cut it into small pieces, and stick it on the plastic strip with double-sided tape.
Embodiment 2
[0028] 1) Prepare buffer solution: Weigh 1.5g sodium dihydrogen phosphate and 70.22g disodium hydrogen phosphate dodecahydrate, add water to make the volume to 1L, and the pH value of the buffer solution is 7.8.
[0029] 2) Weigh 6.14g of 5,5'-dithiobis(2-nitrobenzoic acid) (DNTB) (6.14g / L), 0.32g of disodium ethylenediaminetetraacetic acid (EDTA) (320mg / L L), 15g of 2-methyl-2,4-pentanediol (15g / L), 6g of silicotungstic acid (10g / L), 14g of polyethylene glycol, 1.7g of Triton X-100, 2mL Green (0.1%) dye, add the above components into the prepared buffer;
[0030] 3) After the components prepared in step 2) are completely dissolved, soak the filter paper in the solution, take it out and dry it, cut it into small pieces, and stick it on the plastic strip with double-sided tape.
Embodiment 3
[0031] Preparation and use of embodiment 3 standard color card
[0032] 1) Configure 1mmol / L, 0.5mmol / L, 0.1mmol / L, 0.04mmol / L, 0mmol / L cysteine (Cys) standard solution;
[0033] 2) The cysteine standard solution of each concentration configured in step 1) is immersed in 5 test strips prepared for use, and then taken out;
[0034] 3) Prepare a color comparison card according to the color development after 2 minutes;
[0035] 4) When using, dip the test strip into the sample to be tested and then take it out, add the sample to the reagent bottle according to the sample to be tested, and compare it with the standard color comparison card after 5 minutes of stable color change. The corresponding concentration is the concentration of the solution to be tested. If it is between the two color scales, the concentration of sulfhydryl groups is estimated.
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