Applicable to the rapid determination of three kinds of pesticide residues in tea such as imidacloprid and the test strips used
A technology for pesticide multi-residue and imidacloprid, which is applied in the field of gold-labeled immunoassay detection of small molecular compounds, can solve the problems of inability to quickly screen on-site, excessive chlorinated nicotine pesticides, and high detection false positive rate, and achieves good practicability, High sensitivity, the effect of improving sensitivity
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Embodiment 1
[0043] Embodiment 1: test strip preparation
[0044] 1. Preparation of colloidal gold
[0045] Colloidal gold particles were prepared by trisodium citrate (sodium citrate) reduction method. 150mL 0.01% (mass %) chloroauric acid solution is heated to boiling (about 120 ℃) under the condition of oil bath, add 2.5mL 1% (mass %) trisodium citrate aqueous solution rapidly under magnetic stirring, when the color of solution is completely When it turns bright red, continue to reflux for 5-10 minutes and then stop heating. After cooling, put the solution into a reagent bottle and store it in a refrigerator at 4°C. A colloidal gold solution with a mass concentration of 0.01% was obtained.
[0046] The colloidal gold particles were scanned in the visible light range by a UV-visible spectrophotometer, and the maximum absorption wavelength λmax was measured to be 520nm, and the absorbance value was 0.80; the colloidal gold particles were observed under a transmission electron microsco...
Embodiment 2
[0065] Example 2: Application
[0066] 1. Test strip sensitivity test
[0067] (1) Standard solution preparation
[0068] Standard stock solutions of three pesticides, imidacloprid, clothianidin and chlorothiamid, were prepared with methanol, and the concentrations of the standard stock solutions were all 1 mg / L. Then use 0.01M PBS buffer to dilute imidacloprid, clothianidin, and clothhirid to the standard working solutions of serial concentrations: 0.1mg / L, 0.01mg / L, 0.005mg / L, 0.002mg / L, 0.001mg / L .
[0069] (2) Standard solution detection
[0070] Set 13 treatment groups, respectively blank control (0.01M PBS buffer solution), imidacloprid 0.01mg / L, 0.005mg / L, 0.002mg / L, 0.001mg / L, clothianidin 0.01mg / L, 0.005mg / L L, 0.002mg / L, 0.001mg / L, chlorothialine 0.01mg / L, 0.005mg / L, 0.002mg / L, 0.001mg / L. Use the same batch of residual speed test paper strips for detection, and repeat twice for each treatment group. The detection method is: take a tea soup sample and add 2 drops...
Embodiment 3
[0103] Example 3: Change the "chlorothialine-OVA conjugate" in step 5) of Example 1 to "clothianidin-OVA conjugate", and the clothianidin-OVA conjugate can be prepared according to the following references Obtained: Li M., Sheng E., Cong L., et al., 2013.Development of Immunoassays for Detecting Clothianidin Residue in Agricultural Products.J Agr Food Chem 61(15):3619-3623. Clothianidin hapten and The coupling ratio of OVA is 10:1. The rest of the test strip manufacturing process is identical to Example 1. The sample detection process is equivalent to the step (3) of the applied experiment 1) in Example 2.
[0104] The results obtained are as follows:
[0105] Under the condition of spiked tea soup matrix, the detection sensitivities of imidacloprid, clothianidin and clothiaprid were all 0.005 mg / L, that is, the minimum detection limit was 0.005 mg / L. The results showed that the effect of the detection line coating using heterologous competitive clothianidin-OVA conjugates ...
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