Aflatoxin B1 detection method based on three-dimensional fluorescence
An aflatoxin, three-dimensional fluorescence technology, applied in the direction of fluorescence/phosphorescence, material excitation analysis, etc., can solve the problems of not solving the background spectrum and background drift, not improving the accuracy, not improving the accuracy of the concentration fluorescence peak intensity, etc. Achieve the effect of eliminating baseline drift, good quantitative effect and fast detection speed
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specific Embodiment 2
[0068] The sample detected in this embodiment is soy sauce containing aflatoxin.
[0069] The three-dimensional fluorescent detection of aflatoxin B based on the present embodiment 1 method, including the following steps:
[0070] a. Based on the parallel factor analysis method (PARAFAC), the quantitative analysis model is established according to the standard sample, which is the same as the specific example 1, specifically:
[0071] Step a1, preparing standard samples;
[0072] Step a2, pretreating the standard sample;
[0073] Step a3, using a standard method to quantitatively analyze the standard sample;
[0074] Step a4, using a fluorescence spectrophotometer to measure the standard sample to determine the characteristic area of the EEM spectrum of the standard sample;
[0075] Step a5, establishing a quantitative analysis model for standard samples based on PARAFAC;
[0076] B, quantitative detection is carried out on the sample to be tested, which is the same as ...
specific Embodiment 3
[0097] The samples tested in this embodiment are peanuts containing aflatoxin.
[0098] The three-dimensional fluorescent detection of aflatoxin B based on the present embodiment 1 method, including the following steps:
[0099] a. Based on the parallel factor analysis method (PARAFAC), the quantitative analysis model is established according to the standard sample, which is the same as the specific example 1, specifically:
[0100] Step a1, preparing standard samples;
[0101] Step a2, pretreating the standard sample;
[0102] Step a3, using a standard method to quantitatively analyze the standard sample;
[0103] Step a4, using a fluorescence spectrophotometer to measure the standard sample to determine the characteristic area of the EEM spectrum of the standard sample;
[0104] Step a5, establishing a quantitative analysis model for standard samples based on PARAFAC;
[0105] B, quantitative detection is carried out on the sample to be tested, which is the same as th...
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Abstract
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