Preparation method and application of molecularly imprinted polymer for extracting dencichine
An imprinted polymer and molecular imprinting technology, applied in the field of medicine, can solve the problems of shortening the coagulation time of mice, high price, low purity of Panax notoginseng, etc., and achieve the effects of reliable source of raw materials, simple regeneration method and strong selectivity.
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Embodiment 1
[0034] Preparation of notoginseng pseudo-template molecularly imprinted polymers:
[0035] (1) material preparation
[0036] Each raw material component is formulated according to the following dosage ratio: pseudotemplate molecule phenylpyruvate, functional monomer 4-vinylpyridine 1.66g, crosslinking agent ethylene glycol dimethacrylate 16.12g, initiator azobisisobutyl Nitrile 0.13g, pore forming agent chloroform 45.34g;
[0037] (2) Preparation of polymers with template molecules
[0038] Add the prepared phenylpyruvate, 4-vinylpyridine, ethylene glycol dimethacrylate, azobisisobutyronitrile, and chloroform into the reaction kettle and mix evenly, ultrasonically degas for 15 minutes, and then fill with nitrogen to remove oxygen After sealing for 15 minutes, polymerize in a constant temperature water bath at 60°C for 24 hours to obtain a polymer with template molecules;
[0039] (3) Preparation of molecularly imprinted polymers that remove template molecules
[0040] Grin...
Embodiment 2
[0045] Preparation of notoginseng pseudo-template molecularly imprinted polymers:
[0046] (1) material preparation
[0047] The components of this example are formulated according to the following dosage ratio: template molecule DL-tyrosine 0.91g, functional monoacrylamide 1.83g, crosslinking agent N,N-dimethylbisacrylamide 24.00g, initiator azo Diisobutyronitrile 0.15g, solvent chloroform 50.00g.
[0048] (2) Preparation of polymers with template molecules
[0049] Add DL-tyrosine, acrylamide, N,N-dimethylbisacrylamide, azobisisobutyronitrile and chloroform prepared in step (1) into the reaction kettle and mix evenly, degas it by ultrasonic for 15 minutes, Then fill with nitrogen and remove oxygen for 15 minutes, seal and polymerize in a constant temperature water bath at 60°C for 24 hours to obtain a polymer with template molecules;
[0050] (3) Preparation of molecularly imprinted polymers that remove template molecules
Embodiment 3
[0056] Preparation of notoginseng pseudo-template molecularly imprinted polymers:
[0057] (1) material preparation
[0058] The components of this embodiment are proportioned according to the following dosages: template molecule glycine-DL-leucine 0.85g, functional monomer methacrylic acid 1.66g, crosslinking agent divinylbenzene 21.10g, initiator (azobis Isovaleronitrile) 0.10g, solvent chloroform 47.00g.
[0059] (2) Preparation of polymers with template molecules
[0060] Add glycine-DL-leucine, methacrylic acid, divinylbenzene, azobisisovaleronitrile, and chloroform prepared in step (1) into the reaction kettle and mix evenly, ultrasonically degas for 15 minutes, and then fill with nitrogen to remove Oxygen for 15 minutes, sealed and polymerized in a constant temperature water bath at 60°C for 24 hours to obtain a polymer with template molecules; then grind it through a 200-mesh sieve to obtain molecularly imprinted polymer particles with template molecules notoginsin. ...
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