Nucleic aptamer-based organic arsenic molecular imprinting polymer in marine products, preparation method thereof and application thereof
A nucleic acid aptamer and molecularly imprinted technology, applied in the preparation of organic arsenic molecularly imprinted polymers in seafood, the field of organic arsenic molecularly imprinted polymers in seafood based on nucleic acid aptamers and its preparation can solve the problem of Unsatisfactory detection sensitivity, low practicability, expensive instruments, etc., to achieve good molecular recognition performance, improve sensitivity and selectivity
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Embodiment 1
[0024] The method of the present invention: Weigh 0.4785g functional monomer nucleic acid aptamer, 0.0255g template molecule monomethylarsonic acid, 3.2145g crosslinking agent trimethylolpropane trimethacrylate, 0.0650g initiator azobis Isobutyronitrile and 15ml porogen dichloromethane were mixed uniformly, put into a 25ml ampere flask, bubbling nitrogen for 10 minutes, sealed, and reacted for 48 hours under a 130w high pressure mercury lamp. The polymer monoliths are taken out, ground, extracted, dried, and sieved. Use a methanol: acetic acid (volume ratio 10:1) mixed solution to repeatedly ultrasonically clean the prepared polymer until no template molecule is detected at the maximum absorption wavelength, then clean with methanol to remove excess acetic acid, and dry to obtain a nucleic acid-based A molecularly imprinted polymer of monomethylarsonic acid for gametes.
[0025] Comparative test: Weigh 0.4250g functional monomer acrylic acid, 0.0255g template molecule monomethyl...
Embodiment 2
[0029] The method of the present invention: Weigh 0.4145g functional monomer nucleic acid aptamer, 0.0325g template molecule dimethylarsonic acid, 3.8780g crosslinking agent N,O-diacryloyl-L-amphetamine, 0.0760g initiator couple Nitrogen diisobutyronitrile, 15ml porogen dimethyl sulfoxide, mix well, put into 25ml ampere flask, bubbling with nitrogen for 10 minutes, sealing, and polymerizing under 130w high pressure mercury lamp for 36 hours. The polymer monoliths are taken out, ground, extracted, dried, and sieved. Use acetonitrile: acetic acid volume ratio 25:1 mixture solution to ultrasonically clean the prepared polymer repeatedly until no template molecules can be detected at the maximum absorption wavelength, then wash with methanol to remove excess acetic acid and dry to obtain nucleic acid-based aptamers Molecularly imprinted polymer of dimethylarsine acid.
[0030] Comparative test: Weigh 0.4195g functional monomer 4-vinylpyridine, 0.0325g template molecule dimethylarson...
Embodiment 3
[0034] The method of the present invention: Weigh 0.3685g functional monomer nucleic acid aptamer, 0.0330g template molecule methylarsenic acid, 3.5785g crosslinker divinylbenzene, 0.0655g initiator azobisisobutyronitrile, 15ml The porogen chloroform was mixed uniformly, and filled into a 25ml ampere flask, nitrogen gas was introduced for 10 minutes, sealed, and polymerized under a 130w high pressure mercury lamp for 48 hours. The polymer monoliths are taken out, ground, extracted, dried, and sieved. Use the mixed solution of acetonitrile: acetic acid (volume ratio 15:1) to repeatedly ultrasonically clean the prepared polymer until no template molecule can be detected at the maximum absorption wavelength, then wash with methanol to remove excess acetic acid, and dry to obtain a nucleic acid-based Molecularly imprinted polymer of methylarsenic acid for gametes.
[0035] Comparative test: Weigh 0.4125g functional monomer methacrylic acid, 0.0330g template molecule methylarsenic ac...
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