Low-cost method suitable for rapidly detecting aflatoxin in large-batch edible oil samples
A kind of aflatoxin and edible oil technology, applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve the problems of excessive consumption of organic solvents and cumbersome steps, and achieve the effects of environmental friendliness, good recovery rate, and stable structure
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Embodiment 1
[0036] A low-cost method suitable for the rapid detection of aflatoxins in large quantities of edible oil samples, such as figure 1 As shown, the steps are as follows:
[0037] 1) Weigh 0.5 g of the edible oil sample to be tested and place it in a 5 mL centrifuge tube, dilute the above edible oil sample to be tested with 3 mL of n-hexane, vortex for 1 min, and set aside;
[0038] 2) Take the pine pollen SPE cartridge (500mg, 6mL), activate it with 3mL of n-hexane before use, transfer the sample solution obtained in step 1) into the SPE cartridge, discard the effluent, and realize the extraction of aflatoxin in the sample solution enrichment;
[0039] 3) Continue to add 5mL of n-hexane to rinse the SPE column, then use 5mL of acetone to desorb, and the desorption solution N 2 Blow dry, redissolve with 1.0mL acetonitrile-water (50 / 50, v / v), the obtained solution is the test solution for rapid determination of aflatoxin in edible oil, and perform subsequent HPLC-FLD analysis, t...
Embodiment 2
[0042] In order to verify the feasibility of the low-cost method provided by the present invention that is suitable for the rapid detection of aflatoxin in large quantities of edible oil samples in practical applications, the present embodiment is linear, detection limit (LODs), limit of quantitation ( LOQs) and other parameters were investigated. Two kinds of aflatoxins were prepared into a series of standard mixed solutions of 0.1-20 μg / kg, and analyzed using the HPLC-FLD conditions in Example 1. The concentration of each component was taken as the abscissa, and the corresponding peak area was taken as the ordinate, Establish a calibration curve for aflatoxins. As shown in Table 1, the two aflatoxins have a good linear relationship in the range of 0.1-20 μg / kg, and the square of the regression coefficient (R 2 ) is greater than 0.9987; the detection limit and quantification limit of the two aflatoxins calculated by 3 times and 10 times the signal-to-noise ratio are in the r...
Embodiment 3
[0046] In order to evaluate the accuracy and precision of the low-cost method suitable for rapid detection of aflatoxins in large quantities of edible oil samples provided by the present invention, the recovery rate of the method was investigated in this embodiment. Specific steps are as follows:
[0047] 1) Weigh 0.5g of edible oil sample and place it in a 5mL centrifuge tube, add three concentrations of aflatoxin in low, medium and high concentrations as the edible oil sample to be tested, vortex and mix well, let stand for 30min, and dilute the above-mentioned aflatoxin with 3mL of n-hexane The edible oil sample to be tested, and vortexed for 1min, set aside;
[0048] 2) Take the pine pollen SPE cartridge (500 mg, 6 mL), activate it with 3 mL of n-hexane, transfer the sample solution obtained in step 1) into the SPE cartridge, discard the effluent, and extract and enrich the aflatoxin in the sample solution;
[0049] 3) Add 5 mL of n-hexane to rinse the SPE column, then de...
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