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8 Calculation and presentation of results
The residual amount of the drug to be tested in the sample is calculated according to formula (1.
where:
X - the residual amount of the tested component in the sample, in micrograms per kilogram (μg/kg);
Cs - the concentration of the tested component in the standard solution, in nanograms per milliliter (ng/mL);
A——the peak area of the tested component in the sample solution;
As - the peak area of the measured component in the standard solution;
V——The constant volume of the sample solution, the unit is milliliter (mL);
m—the mass of the sample, in grams (g.
The calculation result needs to deduct the blank valu.
9 Sensitivity, accuracy and precision of detection methods
1 Sensitivity
The detection limit of this method: octylphenol and diethylstilbestrol are respectively 2 μg/kg, nonylphenol and bisphenol A are respectively 1 μg/kg, estrone, 17α-ethinyl estradiol, 17β-estradiol, The estriol was 3 μg/kg, respectively; the limit of quantification: octylphenol and diethylstilbestrol were 5 μg/kg, respectively, nonylphenol and bisphenol A were 3 μg/kg, estrone, 17α-acetylene Estradiol, 17β-estradiol, and estriol were 0 μg/kg, respectivel.
Diethylstilbestrol beta-estradiol
2 Accuracy
Octylphenol and diethylstilbestrol are in the range of 5 μg/kg~10 μg/kg added concentration, and the recovery rate is 70%~110%; Nonylphenol and bisphenol A are in the added concentration range of 3 μg/kg~6 μg/kg, the recovery is The recovery rate is 70%~110%; the recovery rate of estrone, 17α-ethinyl estradiol, 17β-estradiol, estriol is 70%~110% in the range of 0 μg/kg~20 μg/kg added concentratio.
3 Precision
The intra-assay relative standard deviation of this method is less than or equal to 15%, and the inter-assay relative standard deviation is less than or equal to 20.