Method for detecting polyether antibiotics in feed
A technology of polyether antibiotics and detection methods, which is applied in measurement devices, material separation, and analysis of materials, etc., can solve the problems of inability to detect, cumbersome steps, and increased detection workload, and achieves time saving, high sensitivity, and detection results. Accurate and reliable results
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Embodiment 1
[0024] Embodiment 1 The establishment of standard working curve
[0025] (1) Preparation of reaction reagents
[0026] Preparation of monensin standard stock solution: Accurately weigh a certain amount of monensin standard sample, dissolve it in methanol and mix at a constant volume to make the monensin concentration 1mg / ml;
[0027] Preparation of salinomycin standard stock solution: Accurately weigh a certain amount of salinomycin standard sample, dissolve in methanol and mix at a constant volume so that the concentration of salinomycin is 1 mg / ml;
[0028] Preparation of salinomycin standard stock solution: Accurately weigh a certain amount of salinomycin standard sample, dissolve it in methanol and mix at a constant volume so that the concentration of salinomycin is 1 mg / ml;
[0029] Lasalocid sodium standard stock solution preparation: directly use the purchased standard with a concentration of 100 μg / ml, or other concentration standard reference substances can also be u...
Embodiment 2
[0047] Example 2 Verification, addition and recovery detection experiment
[0048] Feed samples without monensin, salinomycin, methyl salinomycin and lasalocid sodium were used as blank samples and crushed into powder. Take by weighing 2g sample in the 50ml centrifuge tube, add appropriate monensin, salinomycin, methyl salinomycin and lasalocid sodium standard solution respectively and make mixed feed sample, make four kinds of antibiotics in mixed feed The concentrations in the final filtrate of the samples were 10, 20, 60 μg / ml, respectively. Converted to the concentrations in the mixed feed samples were 5, 10, 30 mg / kg.
[0049] Add 10ml of 10% methanol solution by volume to the above mixed feed sample, shake it on a vortex mixer for 5 minutes, let it stand for 10 minutes, then centrifuge it at a speed of 5200r / min for 10 minutes, take the supernatant, and repeat the above extraction step once. The two supernatants were combined and dried with nitrogen to obtain a resid...
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