Colloidal gold immune test paper for rapid detection of dibutyl phthalate as well as preparation method and application thereof
A technology of dibutyl phthalate and colloidal gold, which is applied in the field of rapid detection of residual immunochemistry, can solve the problems of fast and simple detection of agricultural products, not suitable for rapid detection on site, and small amount of samples for one detection. The effect of fast speed, short detection time and low cost
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Embodiment 1
[0037] The colloidal gold immunoassay paper for rapid detection of dibutyl phthalate of the present invention comprises a reaction membrane 2, a sample pad 3, a conjugate release pad 4, a water-absorbing pad 5 and a backing 1, and is wrapped on the reaction membrane 2. Test area 6 with dibutyl phthalate-carrier protein conjugate and quality control area 7 with goat anti-mouse IgG, conjugate release pad 4 coated with dibutyl phthalate monoclonal antibody-colloid Gold marker 8.
[0038] In this embodiment, the sample pad 3 , the conjugate release pad 4 , the reaction membrane 2 and the water-absorbing pad 5 are sequentially arranged on the backing 1 .
[0039] Dibutyl phthalate-carrier protein conjugate is obtained by nitrating and reducing dibutyl phthalate to form 4-aminodibutyl phthalate hapten, and then coupling with carrier protein. Wherein, the carrier protein in the dibutyl phthalate-carrier protein conjugate is bovine serum albumin. Dibutyl phthalate monoclonal antibod...
Embodiment 2
[0041] Colloidal gold immunoassay paper preparation method for rapid detection of dibutyl phthalate of the present invention comprises the following steps:
[0042] 1. Synthesis and identification of dibutyl phthalate-carrier protein conjugates
[0043] (1) Synthesis of 4-aminophthalate-dibutyl-bovine serum albumin
[0044] Dissolve 100mg of carbodiimide in 3.0ml of 10mol / L PBS solution with pH 8.0 (referred to as 1 solution); take 10mg of 4-aminodibutylphthalate and dissolve it in 1ml of dimethylformamide (2 solutions) ; Dissolve 20 mg of bovine serum albumin in 1ml of 10mol / L PBs (pH8.0) solution (3 solutions); mix (2 solutions) with (3 solutions), and gradually add (1 solution) under magnetic stirring, Stir at 4°C for 12h. Distilled water was used to fully dialyze it for 4-6 days to obtain the immune antigen.
[0045] 2. Preparation of dibutyl phthalate monoclonal antibody
[0046] (1) Animal immunity
[0047] The immunized antigen was injected into Balb / c mice at an i...
Embodiment 3
[0066] Example 3: Detection of residues in samples
[0067] 1. Sample pretreatment
[0068] Weigh 50g of chicken, pork, pork liver, sausage, fish, shrimp, honey, puffed food, etc., homogenate, put into a stoppered conical flask, add 100ml of extractant (methanol, ethyl acetate, etc.), extract for 1h . Centrifuge, take the supernatant, concentrate to 1ml, and dilute with PBS or normal saline.
[0069] 2. Detection with test paper card
[0070] Drop the sample into the hole of the reagent card with a dropper, add 3 drops, count the time after adding, and observe the result within 5-8 minutes. The detection and interpretation of samples exceeding 10 minutes is invalid.
[0071] 3. Analysis of test results
[0072] Positive: When the (C) area shows a red band, but the (T) area does not show color, it is judged as positive.
[0073] Negative: When (C) area shows a red band, (T) area also shows a red band, and the color of (T) area is close to or lighter than that of (C) area,...
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