Application of hyperbranched polyglycerol modified nanosphere to immunochromatography
A technology of glycidyl ether and hyperbranched polymer, which is applied in the field of biomedical diagnosis, can solve the problems of limited application, weak binding ability, and low coupling efficiency, and achieve the effects of reducing non-specific binding, broadening the detection range, and improving detection quality
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Embodiment 1
[0042] Example 1: Preparation method of hyperbranched polyglycidyl ether modified nanosphere dry immunochromatography test strip
[0043] 1. Preparation of hyperbranched polyglycidyl ether modified nanospheres:
[0044] 1) Preparation of hyperbranched polyglycidyl ether: In a three-necked flask equipped with mechanical stirring and a micro constant flow pump, add 0.24g trimethylol propane (TMP) as the initiator of the reaction, using 3.7M potassium methylate (CH3OK) deprotonates the hydroxyl part of TMP, the deprotonated part accounts for 10% of the total part, and the excess methanol is removed by heating and evaporating; then slowly add 50ml of glycidol into the system to initiate polymerization, pay attention to the dropping speed, too fast may Cause implosion, reaction temperature 95°C, reaction time 12h;
[0045] After the reaction, the product was dissolved in methanol and passed through a strong acid cation exchange resin (AMBERJET TM 1500H Resin) polymer is precipit...
Embodiment 2
[0056] The method for making test strips as a control group in embodiment 2 is the same as the above method, except that commercialized polystyrene microspheres (the same as the experimental control, the manufacturer's JSR diagnostic reagent, article number MS 160 / Carboxyl) do not hyperbranched grooming. Example 2: Evaluation of detection indicators of hyperbranched polyglycidyl ether modified nanospheres dry immunochromatography test strips
[0057] The performance analysis of the reagents was carried out on the cardiac troponin I (cTnI) project using hyperbranched glycidyl ether modified nano-microsphere immunochromatographic test strips. The experiment on the I(cTnI) project was used as a control group. During the experiment, 50ul of the analyte was added from the sample pad, and after 15min, its fluorescence value was measured by Getein1100 fluorescence immunoassay analyzer (Nanjing Jidan Biotechnology Co., Ltd.), and then Calculate its related performance indicators.
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