Aflatoxin B1 graphene oxide immunochromatographic test strip and application thereof
A technology for immunochromatographic test strips and aflatoxins, which is applied in analytical materials, measuring devices, instruments, etc., can solve the problems of reducing the cost of test strips, uniformity between batches and marketization, small batch output and high cost.
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[0061] The preparation of carboxylated graphene oxide solution can adopt following method:
[0062] Pass 3.0g of flake graphite through a 325 mesh sieve and add it to 400mL of a mixed solution of sulfuric acid and phosphoric acid with a volume ratio of 9:1, and stir for 10 minutes; More, to avoid the reaction temperature exceeds 20 ℃. After all the potassium permanganate was added, it was heated to 50°C and stirred for 12 hours. After the reaction, let the mixture cool down to room temperature naturally, pour it into ~400mL of ice water, keep stirring at room temperature for 0.5 hours, add 30% hydrogen peroxide dropwise to the reaction system until the solution turns bright yellow and stops. Let it stand overnight, discard the supernatant, wash 3 times with 1L of hydrochloric acid with a mass fraction of 5%-10%, and then wash 5 times with 1L of deionized water to remove metal ions, sulfate ions and chloride ions, and finally the obtained The solid was freeze-dried, then plac...
Embodiment 1-2
[0064] Example 1-2: Preparation and application of graphene oxide immunochromatographic test strip for rapid detection of aflatoxin B1
Embodiment 1
[0066] The preparation method of rapid detection aflatoxin B1 graphene oxide immunochromatographic test strip comprises the following steps:
[0067] Preparation of chromatography test strips:
[0068] (1) Preparation of absorbent pad
[0069] Cut the absorbent paper to a size of 42mm and 3mm wide to obtain an absorbent pad;
[0070] (2) Preparation of detection pad
[0071] The coating of the detection line:
[0072] The aflatoxin B1-bovine serum albumin conjugate AFB1-BSA was prepared with coating buffer to make a coating solution of 0.7mg / mL; at a position 8mm away from the upper edge of the sample pad, it was coated horizontally by line spraying. Coated on a nitrocellulose membrane to obtain a detection line, the coating amount of aflatoxin B1-bovine serum albumin conjugate required per centimeter of detection line is 420ng, and then dried at 37°C for 45 minutes;
[0073] The coating buffer is: 1g bovine serum albumin, 0.02g sodium azide, 0.8g sodium chloride, 0.29g di...
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