Multi-template monodisperse active notoginsenoside molecular imprinted polymer and preparation method thereof
A molecular imprinting and template molecule technology, applied in the field of bioengineering, to achieve the effects of reduced damage, uniform particle size and high yield
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Embodiment 1
[0035] 348.5mg ginsenoside Rb 1 , Ginsenoside Rg 1 and notoginsenoside R 1 The mixture (the molar ratio of the three is 44:43:13) and 1.00mmol functional monomer MAA were dissolved in 25mL DMF solvent, dissolved by ultrasonication for 10min, and pre-polymerized for 2-4h. Then add 6.00 mmol of cross-linking agent EGDMA and 48.72 mg of initiator AIBN, and dissolve by ultrasonication for 10 min. The mixed solution was blown with nitrogen gas for 10 minutes, heated to 60° C. on a constant temperature shaker, and polymerized at 300 rpm for 24 hours.
[0036] Collect by centrifugation and elute with methanol-glacial acetic acid (v / v, 9:1) to remove template molecules until no template molecules can be detected at 204nm by UV spectrophotometer, then wash with methanol until neutral, and then 45°C After vacuum drying for 12 hours, the multi-template monodisperse notoginseng active saponin molecularly imprinted polymer (MIP-1) was obtained.
[0037] No template molecule notoginseng...
Embodiment 2
[0039] 348.5mg ginsenoside Rb 1 , Ginsenoside Rg 1 and notoginsenoside R 1 The mixture (the molar ratio of the three is 44:43:13) and 1.50mmol functional monomer AU were dissolved in 30mL THF solvent, dissolved by ultrasonication for 10min, and pre-polymerized for 2-4h. Then add 6.00 mmol of cross-linking agent TRIM and 75.88 mg of initiator AIBN, and dissolve by ultrasonication for 5 min. The mixed solution was blown with nitrogen gas for 10 minutes, heated to 50° C. on a constant temperature shaker, and polymerized at 200 rpm for 36 hours.
[0040] Collect by centrifugation and elute with methanol-glacial acetic acid (v / v, 9:1) to remove template molecules until no template molecules can be detected at 204nm by UV spectrophotometer, then wash with methanol until neutral, and then 45°C After vacuum drying for 24 hours, the multi-template monodisperse notoginseng active saponin molecularly imprinted polymer (MIP-2) was obtained.
[0041] No template molecule notoginseng sa...
Embodiment 3
[0043] 348.5mg ginsenoside Rb 1 , Ginsenoside Rg 1 and notoginsenoside R 1 The mixture (the molar ratio of the three is 44:43:13) and 2.00mmol functional monomer AM were dissolved in 40mL ethanol solvent, dissolved by ultrasonication for 10min, and pre-polymerized for 2-4h. Then add 10.00 mmol of cross-linking agent EGDMA and 74.20 mg of initiator AIBN, and dissolve by ultrasonication for 10 min. The mixed solution was blown with nitrogen for 10 minutes, heated to 60° C. on a constant temperature shaker, and polymerized at 200 rpm for 24 hours.
[0044] Collect by centrifugation and elute with methanol-glacial acetic acid (v / v, 9:1) to remove template molecules until no template molecules can be detected at 204nm by UV spectrophotometer, then wash with methanol until neutral, and then 45°C After vacuum drying for 24 hours, the multi-template monodisperse notoginseng active saponin molecularly imprinted polymer (MIP-3) was obtained.
[0045] No template molecule notoginseng...
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