A kind of sibutramine magnetic molecularly imprinted polymer and its preparation method
A magnetic molecular imprinting and molecular imprinting technology, applied in the directions of alkali metal compounds, chemical instruments and methods, and other chemical processes, can solve the problems of increased detection cost, high maintenance cost, high cost, etc., and achieve simple operation and reduce interference. Effect
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Embodiment 1
[0025] Embodiment 1: Magnetic nanoparticles (Fe 3 o 4 SiO 2) preparation:
[0026] At room temperature, add 80 mL of deoxygenated deionized water into a 250 mL three-necked bottle, and keep the stirring speed at 800 rpm -1 , FeCl was added under the protection of nitrogen 2 4H 2 O (1.72g) and FeCl 3 ·6H 2 O (4.72g), when the temperature rises to 80°C, add ammonia water (28%wt) 10mL dropwise, react for 1h, then add PEG-2002mL, stir for 10min, magnetically separate, wash with deionized water until neutral, and obtain Fe 3 o 4 Magnetic nanoparticles, dispersed in isopropanol for later use.
[0027] Take Fe 3 o 4 Magnetic nanoparticles 0.3g, dispersed in 50mL isopropanol, ultrasonic 15min. Keep stirring speed 200rmpmin -1 , add deionized water 2mL and ammonia water (28%wt) 2mL, with 20μLmin -1 Add 5 mL of tetraethyl orthosilicate (TEOS) at a high speed, react at room temperature for 12 hours, wash with deionized water until neutral, and dry in vacuum to obtain magneti...
Embodiment 2
[0036] Embodiment 2: the preparation of MMIPs (method 2)
[0037] With embodiment 1, difference is: take the Fe of functionalization modification 3 o 4 SiO 2 Nanoparticles 40 mg, 1 mmol of (±) N-{1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutyl}-N-methyl-N-methacrylamide, 3 mmol The functional monomer 4-vinylpyridine was uniformly dispersed in 100mL of toluene-acetonitrile (9:1, v / v), and stirred at room temperature for 1h prepolymerization; then 6mmol of crosslinking agent trimethylolpropane trimethacrylate ( TMPTMA) and 80 mg of initiator azobisisobutyronitrile (AIBN), nitrogen gas was passed for 15 minutes to remove oxygen and then sealed, heated to 50°C for 6 hours; then heated to 60°C for 24 hours; and finally reacted at 85°C for 6 hours. The obtained MMIPs were separated under an external magnetic field, and the template molecules were repeatedly eluted with 1M hydrochloric acid solution to remove template molecules, then washed with methanol until neutral, and the poly...
Embodiment 3
[0038] Embodiment 3: selective adsorption test
[0039] Accurately weigh several portions of 20mg MMIPs and MNIPs dispersed in 10mL of 2.0mM sibutramine and its active metabolite M 1 and M 2 Shake the toluene-acetonitrile (9:1, v / v) solution at room temperature for 1 h in a constant temperature oscillator, then magnetically separate, take the supernatant, and measure the concentration of the sample solution before and after adsorption by HPLC-UV. According to the concentration of the solution before and after binding , and calculate the adsorption capacity of MMIPs and MNIPs for different compounds ( image 3 ), sibutramine MMIPs (method 2) have a good adsorption effect on sibutramine, sibutramine metabolite M1, and sibutramine metabolite M2, and its adsorption capacity is much larger than that of MNIPs. It shows that sibutramine MMIPs have a specific recognition effect on sibutramine and its metabolite molecules.
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