A high-throughput screening and analysis method for organic pollutants in blood
A technology for organic pollutants and analysis methods, which is applied in the field of high-throughput screening and analysis of organic pollutants in blood, can solve problems such as cumbersome processing methods, and achieve the advantages of less sample demand, good application value, and simplified extraction and purification steps. Effect
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Embodiment 1
[0065] In order to verify whether the method for building a library used in the present invention can accurately detect the organic pollutants to be detected, the polluted blood is simulated in Example 1, and different types of organic pollutants are added to the clean blood in a specific amount. After the method was identified, the accuracy of the method was verified by the spectrum of the standard substance.
[0066] The blood sample containing organic pollutants in this example is as follows: take 3 parts of 0.5mL blood samples in a 15mL centrifuge tube, add 50 μL of 30 kinds of organic pollutants with a concentration of 100ppb, vortex and mix them and let stand for 12h, 30 kinds of organic pollutants Substances are common substances widely used in industries such as pesticides, pharmaceuticals, and flame retardants (Table 1).
[0067] A high-throughput screening and analysis method for organic pollutants in blood according to the present invention:
[0068] (1) Extraction...
Embodiment 2
[0100] (1) Extraction of pollutants in blood: take 16 parts of 0.5mL fish blood samples in a 15mL centrifuge tube, add 0.3gMgSO 4 -NaCl mixture (used as SPE) and 1.5mL acetonitrile were mixed on a vortex for 30s (to ensure the infiltration of the SPE material), sonicated for 30min and then centrifuged; the supernatant was transferred to another clean centrifuge tube, and the solid residue was washed with 1.5 mL acetonitrile Repeat the above extraction step twice, and combine the supernatants.
[0101] (2) Concentration and constant volume: Concentrate the extract and slowly purge the solvent with high-purity nitrogen; use 100 μL acetonitrile for constant volume, if there is a small amount of white solid at the bottom after constant volume (during the supernatant transfer process Part of the water phase may move into it, in which saturated MgSO is dissolved 4 and NaCl), it needs to be centrifuged again, and finally the supernatant is transferred to a brown sampling vial and st...
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