Detection method for 1-aminohydantoin hydrochloride in animal tissues and detection card
A technology of nitrofurazone and animal tissue, which is applied in the field of detection of nitrofurazone metabolites, can solve problems affecting the detection efficiency of nitrofurazone, achieve the effects of eliminating extraction and reconstitution, simple detection process, and improved accuracy
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Embodiment 1
[0026] A detection card for nitrofurazone metabolites in animal tissues, comprising a detection card and a reagent, the surface of the detection card is provided with a colloidal gold test strip, and the inner side of the detection card is respectively provided with a sample hole and a mold standard hole, so A monoclonal colloidal gold-labeled antibody of freeze-dried nitrofurazone metabolites is provided on the inner side of the mold standard well, and a contrasting color block is equidistantly arranged on the top of the surface of the detection card, and a flow-limiting bump is provided at the bottom of the contrasting color block, and the The current-limiting bump is located on the top of the sample hole and mold standard hole. The reagents include animal tissue, deionized water, 1M hydrochloric acid, derivatization reagent, extraction agent, 1M sodium hydroxide, gold chloride, double distilled water, chlorine Auric acid solution, 1% sodium citrate aqueous solution, 0.1mol / L...
Embodiment 2
[0028] A detection method for nitrofurazone metabolites in animal tissue, comprising the following steps:
[0029] S1. Weigh crucian carp back tissue, chicken leg tissue and chicken back tissue and mince them with a meat grinder, and take 1-3g samples to be tested with tweezers and put them into different centrifuge tubes;
[0030] S2. Use a test tube to measure 3-5ml of deionized water, 0.3-0.6ml of 1M hydrochloric acid, 0.1-0.3ml of derivatization reagent, 3-6ml of extractant, and 0.3-0.5ml of 1M sodium hydroxide. Take 3-5ml of deionized water, 0.3-0.6ml of 1M hydrochloric acid, and 0.1-0.3ml of derivatization reagent into the centrifuge tube, and let the sample to be tested in the centrifuge tube be mixed with 3-5ml of deionized water, 0.3- 0.6ml of 1M hydrochloric acid, 0.1-0.3ml of derivatization reagent, shake and mix for 3-5min, incubate in a water bath at 55-60°C for 30min, then add 3-6ml of extractant, 0.3-0.5ml of 1M hydroxide Sodium, put it in a centrifuge at 4000r...
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