Quetiapine artificial hapten, artificial antigen and preparation method and application thereof
An artificial hapten, artificial antigen technology, applied in chemical instruments and methods, animal/human peptides, animal/human proteins, etc., can solve the problems of artificial hapten and artificial antigen without quetiapine
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Embodiment 1
[0049] The preparation method of this implementation a kind of quetiapine artificial antigen (reaction course is as follows: figure 1 ), including the following steps:
[0050] (1) Preparation of artificial hapten:
[0051]① Weigh 200mg (0.45mmol) of quetiapine fumarate into a 50ml conical centrifuge tube, add 20ml of purified water to dissolve, and then add concentrated ammonia water to adjust the pH of the solution to 9. At this time, a large amount of white precipitate appears. Extracted with 20ml of dichloromethane each time, a total of three extractions, collected the organic phase, dried over anhydrous magnesium sulfate, filtered, and evaporated to dryness under reduced pressure to obtain 170mg (0.44mmol) of pale yellow oily substance A;
[0052] The light yellow oily product A was detected by TLC, and the chromatographic solution was dichloromethane: 95% ethanol: 1,4-dioxane: ammonia water=10:8:1:1 (v / v), product Rf= 0.8;
[0053] ②Put 170mg (0.44mmol) of light yello...
Embodiment 2
[0125] The performance measurement of embodiment 2 quetiapine artificial antigen
[0126] (1) Identification of quetiapine artificial antigen:
[0127] Molar absorption coefficient ε: quetiapine artificial hapten solutions with concentrations of 0 μg / ml, 5 μg / ml, 10 μg / ml, 20 μg / ml, 30 μg / ml, and 40 μg / ml were prepared in PBS buffer, and the quetiapine The maximum absorption wavelength of the thiopine hapten is 263nm, the absorbance value is measured at 263nm, and parallel samples are made for each concentration. The formula for calculating the molar absorptivity (ie, the molar absorptivity) is: ε=absorbance value / molar concentration.
[0128] Determination of conjugate protein concentration: Prepare the concentration of 0μg / ml, 10μg / ml, 20μg / ml, 30μg / ml, 40μg / ml, 60μg / ml, 80μg / ml, 100μg / ml, 120μg / ml in PBS buffer Add 3ml of Coomassie Brilliant Blue staining solution to 1ml of bovine gamma globulin solution, mix immediately, warm in a 30°C water bath for 5 minutes, make para...
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