Method for detecting phytic acid based on carbon dot fluorescence off-on mode
A phytate and carbon dot fluorescence technology, applied in the analysis and detection of phytate, based on the carbon dot fluorescence off-on mode detection of phytate field, can solve the problem that liquid chromatography equipment is expensive, operators Need professional training, poor selectivity and sensitivity, etc., to shorten the sample detection time, improve the sample detection efficiency, and easy to operate.
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Embodiment 1
[0026] Taking phytate contained in corn seeds as the detection object, the specific operation steps are as follows:
[0027] (1) Preparation of carbon dot fluorescent probe: 4.2 g of citric acid and 2.1 g of lysine were added to 40 mL of ultrapure water. After stirring for 2 to 3 minutes, add it to the reaction kettle. The mixed solution was reacted at 200° C. for 5 hours. After the reaction, the solution was dialyzed in pure aqueous solution for 36 hours to remove impurities, and the carbon dots obtained by dialyzing were diluted to 0.2 mg / L with 10 mmol / L (pH=5.7) morpholineethanesulfonic acid buffer;
[0028] (2) Prepare phytic acid standard solution: use 10mmol / L (pH=5) morpholine ethanesulfonic acid buffer to prepare standard sample stock solution of phytic acid, the stock solution concentration is 0.1mmol / L to 10mmol / L L, the stock solution is configured into standard solutions of different concentrations with morpholinoethanesulfonic acid buffer solution;
[0029] (3...
Embodiment 2
[0034] The specific operation steps are as follows:
[0035] (1) Preparation of carbon dot fluorescent probes: 4.2 g of citric acid and 1.4 g of lysine were added to 40 mL of ultrapure water. After stirring for 2 to 3 minutes, add it to the reaction kettle. The mixed solution was reacted at 200° C. for 5 hours. After the reaction, the solution was dialyzed in pure aqueous solution for 36 hours to remove impurities, and the carbon dots obtained by dialyzing were diluted to 0.1 mg / L with 10 mmol / L (pH=5.7) morpholineethanesulfonic acid buffer;
[0036](2) Prepare phytic acid standard solution: use 10mmol / L (pH=6) morpholine ethanesulfonic acid buffer to prepare standard sample stock solution of phytic acid, the stock solution concentration is 0.1mmol / L to 10mmol / L L, the stock solution is configured into standard solutions of different concentrations with morpholinoethanesulfonic acid buffer solution;
[0037] (3) Fluorescence quenching: add 20μL 10mM FeCl to 2mL 0.1mg / L carb...
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