Detection method of steroid hormone
A steroid hormone and detection method technology, applied in the field of steroid hormone detection, achieves high precision and accuracy
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Embodiment 1
[0034] A detection method for steroid hormones, comprising the following steps:
[0035](1) Sample pretreatment: 0.75g of seawater sediment (taken from the coastal waters of Guangxi) was added to 25mL of solvent for ultrasonic extraction, wherein the solvent was methanol, ethylene glycol derivatives and acetic acid with a volume ratio of 1:0.5:1 Ethyl ester, then ultrasonically extract at 35°C for 15min, repeat 3 times, combine the extracts to obtain an organic extract; use a rotary evaporator to perform rotary evaporation to obtain an organic concentrate, wherein the content of organic solvent is <25%; The concentrated solution was re-dissolved in methanol, wherein the volume ratio of the organic concentrated solution to methanol was 1:1.5, and filtered through a 0.22 μm organic phase filter head to obtain the sample filtrate;
[0036] Install the solid-phase extraction column, activate the solid-phase extraction column with 5mL methanol and 5mL ultrapure water in sequence, a...
Embodiment 2
[0039] A detection method for steroid hormones, other steps are the same as in Example 1, and the difference from Example 1 is: in step (1) sample pretreatment, ultrasonic extraction solvent methanol, ethylene glycol derivatives and ethyl acetate The volume ratio is 1:1:1.
Embodiment 3
[0041] A detection method for steroid hormones, other steps are the same as in Example 1, and the difference from Example 1 is: in step (1) sample pretreatment, a solid-phase extraction column is installed, and activated with 8mL methanol and 8mL ultrapure water successively For the solid phase extraction column, adjust the appropriate vacuum degree, pass 250 μL of the above sample filtrate through the column at a constant flow rate of 3 mL / min, after the sample is loaded, rinse the solid phase extraction column with ultrapure water, and place the extraction column at 40 °C under nitrogen Blow dry, then use 8mL ethyl acetate, 8mL acetonitrile, 8mL ultrapure water eluent to elute the solid phase extraction column successively, the elution rate is 0.5 drops / s, obtain the eluent, and the eluent is constant volume with methanol 2mL, through a 0.22μm microporous membrane, to be tested.
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