Color-fluorescence dual-function immunochromatography test strip and preparation method thereof
An immunochromatographic test strip, dual-function technology, applied in analytical materials, measuring devices, instruments, etc., can solve the problems of low detection sensitivity, inability to quantify, unable to provide accurate concentration data, etc., and achieve high detection sensitivity and high detection accuracy. Effect
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[0043] A preparation method of a color-fluorescence dual-function immunochromatographic test strip comprises the following steps:
[0044] (I) Preparation of sample pad 2
[0045] Soak glass fiber, polyester film, sponge or filter paper in PBS buffer solution containing EDTA, tween-20, PVP and BSA, then dry in an oven, seal and dry for future use;
[0046] (II) Preparation of marker-binding pad 3
[0047] Soak the glass fiber or polyester film with PBS buffer containing trehalose, bovine serum albumin, tween-20 and PVP, then dry it in an oven, and then spray the color-fluorescent dual-functional microsphere marker probe on the Treat the dried glass fiber or polyester film, place it in an oven for drying again, and store it in a sealed and dry place for later use.
[0048] The specific preparation method of the above-mentioned color-fluorescent dual-functional microsphere marker probe is as follows:
[0049] (a) Preparation of microspheres: Dissolve one of polystyrene, polym...
Embodiment 1
[0061] Aflatoxin M1 blue-time-resolved fluorescent dual-function immunochromatographic test strip
[0062] 1. Preparation method of test strips
[0063] (a) Preparation of microspheres
[0064] Dissolve 8 mmol of styrene monomer and 0.8 mmol of acrylic acid monomer in 10 ml of deionized water containing 0.3 mmol of sodium dodecylsulfonate, add the mixture into a round bottom flask, and stir evenly with a magnetic stirring bar. Then use high-purity nitrogen to remove the air in the round-bottomed flask, seal and heat to 70°C, add 0.3ml of 0.2mmol potassium persulfate, seal the flask with oxygen and stir for 8 hours, then cool down to room temperature. Then filter the reaction solution with a filter paper with a pore size of 8 μm, collect the filtrate and centrifuge and purify it. The centrifugation condition is 50,000 g at 10°C for 15 minutes at a constant temperature, remove the supernatant, redissolve the precipitate with 5 ml of deionized water, wash repeatedly three times,...
Embodiment 2
[0102] Chloramphenicol red-rhodamine fluorescent dual-function immunochromatographic test strips
[0103] 1. Preparation method of test strips
[0104] (a) Synthesis of microspheres
[0105] Dissolve 8 mmol of styrene monomer and 0.8 mmol of acrylic acid monomer in 10 ml of deionized water containing 0.3 mmol of sodium dodecylsulfonate, add the mixed solution into a round bottom flask, and stir evenly with a magnetic stirring bar. Then use high-purity nitrogen to remove the air in the round-bottomed flask, seal and heat to 70°C, add 0.3ml of 0.2mmol potassium persulfate, seal the flask with oxygen and stir for 8 hours, then cool down to room temperature. Then filter the reaction solution with a filter paper with a pore size of 8 μm, collect the filtrate and centrifuge and purify it. The centrifugation condition is 50,000 g at 10°C for 15 minutes at a constant temperature, remove the supernatant, redissolve the precipitate with 5 ml of deionized water, wash repeatedly three ti...
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