Fluorescent rapid screening method for benzopyrene in food
A technology for food and benzos, which is applied in the field of fluorescence rapid screening of benzopyrene in food, can solve the problems of large sample loss and complicated experimental process, and achieves the effects of simple operation, low cost and reduction of pretreatment process.
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Embodiment 1
[0034] Sea oyster cake sample: After the sea oyster cake is ground, weigh 5g, wrap the sample in a filter paper, put it into a reagent bottle, soak it in 50mL of dichloromethane, let it stand, take out the supernatant with a straw, and transfer it into the fluorescence spectrophotometer. Conventional quartz fluorescence sample cell, for derivative-constant energy simultaneous fluorescence spectrum mapping. The instrument parameters are set as follows: constant energy difference Δv=1400cm -1 ; The scanning start excitation wavelength is 250nm, and the scanning stop wavelength is 600nm. get as figure 1 The constant energy synchronized fluorescence spectrum shown by figure 1 The benzo(a)pyrene peaks shown can be used for the identification and rough determination of benzo(a)pyrene.
Embodiment 2
[0036] Similar to Embodiment 1, the difference is that the second-order derivation function is added to obtain as figure 2 Derivative-constant energy synchronized fluorescence spectra shown. The signal intensity values at 384 and 394nm of the spectrum were respectively read by the adjacent peak-valley method, and the sum of their absolute values was the derivative fluorescence intensity for quantitative calculation. At the same time, take another 5 parts of the supernatant, add benzo(a)pyrene standard solution, and measure the derivative-constant energy synchronous fluorescence spectrum in the same way. Mapping such as image 3 standard addition curve. The linear fitting equation of the standard addition curve is Y=144.4+72.0*X, the correlation coefficient is 0.9992, and the linearity is good. Thus, the supernatant liquid contained 2.01 ng / mL of benzo(a)pyrene, which was converted into 20.1 μg / kg of benzo(a)pyrene in the sea oyster cake sample.
Embodiment 3
[0038] Shredded meat sample: cut the sample into pieces, grind it, weigh 5g, wrap it with filter paper, soak it in 25mL of dichloromethane solvent, place it, take out the supernatant with a straw, and transfer it to the conventional quartz fluorescence sample cell of the fluorescence spectrophotometer , for simultaneous fluorescence detection at constant energy. The instrument parameters are set as follows: constant energy difference Δv=1400cm -1 ; The scanning start excitation wavelength is 250nm, and the scanning stop wavelength is 450nm. get as Figure 4 The constant energy synchronous fluorescence spectrum shown can be used for the identification and rough determination of benzo(a)pyrene from the illustrated peak of benzo(a)pyrene. Adding the second-order derivation function, we get as Figure 5 Derivative-constant energy synchronized fluorescence spectra shown. The signal intensity values at 384 and 394nm of the spectrum were respectively read by the adjacent peak-v...
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