Rapid detecting method and corresponding test strip for acetamiprid residues in tea
A technology of acetamiprid and test strips, which is applied in the field of pesticide residue gold standard speed test strips, can solve the problems of high detection false positive rate, inability to quickly screen on-site, detection requires multi-step reactions, etc., and achieves high detection sensitivity , good practicability, and the effect of improving sensitivity
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Embodiment 1
[0051] Embodiment 1: Preparation of acetamiprid gold standard speed test paper strip:
[0052] 1. Preparation of colloidal gold
[0053] Colloidal gold particles were prepared by sodium citrate (trisodium citrate) reduction method. 150mL0.01% (mass %) chloroauric acid solution is heated to boiling (about 120 ℃) under oil bath condition, under magnetic stirring, add 2.5mL1% (mass %) sodium citrate aqueous solution rapidly, 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.
[0054] 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; and the colloidal gold particles were observed und...
Embodiment 2
[0074] Example 2: Application
[0075] 1. Test strip sensitivity test
[0076] (1) Standard solution preparation
[0077] Prepare the standard stock solution of acetamiprid with methanol, the concentration of the standard stock solution is 1mg / L. Then dilute acetamiprid with 0.01MPBS buffer solution to a series concentration of standard working solution 0.1mg / L, 0.01mg / L, 0.005mg / L, 0.002mg / L.
[0078] (2) Standard solution detection
[0079] Set up 4 treatment groups, respectively blank control (0.01MPBS buffer solution), acetamiprid 0.01mg / L, 0.005mg / L, 0.002mg / L standard working solution. 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 to the spotting hole for chromatographic reaction. After 5 to 10 minutes, according to the detection The color development of line 5 and quality control line 6 can directly determine the positive and negative re...
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