Method for purifying erythromycin by using molecular engram polymer
A technology of molecular imprinting and erythromycin, which is applied in separation methods, chemical instruments and methods, preparation of test samples, etc., can solve the problem of no erythromycin molecular imprinting polymer solid-phase extraction column, etc., and achieve high selectivity Good sex, specificity, and sensitivity-enhancing effect
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Embodiment 1
[0023] 1. Preparation of erythromycin molecularly imprinted polymer:
[0024] Mix erythromycin (template) 0.5mol, monomer methacrylic acid (MAA), and crosslinking agent ethylene glycol dimethacrylate (EGDMA) according to the molar ratio of 1:2:20, and dissolve to 2.5ml Porogen (acetonitrile: methanol = 3: 2), placed in an ampoule, then added 0.02 g of initiator azobisisobutyronitrile (AIBN), ultrasonicated for 5 minutes, then flushed with nitrogen for 5 minutes, and vacuum sealed. Water bath at 60°C for 24 hours to obtain erythromycin molecularly imprinted polymer. Take out the blocky polymer, grind it with a mortar, sieve it to an average particle size of 30-60 μm, suspend it with acetone and discard the fine particles. After the polymer was dried, the template was removed by Soxhlet extraction with methanol (containing 10% acetic acid) for 72 hours, and the medium was changed every 8 hours. Take 20 ul of the eluate, and after HPLC determines that the elution is complete, d...
Embodiment 2
[0030] 1. Preparation of erythromycin molecularly imprinted polymer:
[0031] Mix 0.5 mol of erythromycin (template), monomer methacrylic acid (MAA), and cross-linking agent ethylene glycol dimethacrylate (EGDMA) according to the molar ratio of 1:4:20, and dissolve until 5ml Pore agent (acetonitrile: methanol = 3: 2), placed in an ampoule, then added 0.02 g of initiator azobisisobutyronitrile (AIBN), ultrasonicated for 5 minutes, then flushed with nitrogen for 5 minutes, vacuum sealed, 60 ℃ water bath for 36 hours to obtain erythromycin molecularly imprinted polymer. Take out the blocky polymer, grind it with a mortar, sieve it to a particle size of 30-60 μm, suspend it with acetone and discard the fine particles. After drying the polymer, use methanol (containing 10% acetic acid) for Soxhlet extraction for 48 hours to remove the template and change the solution every 8 hours. After the elution was complete as determined by HPLC, it was dried at 60° C. for 24 hours for lat...
Embodiment 3
[0038] 1. Preparation of erythromycin molecularly imprinted polymer:
[0039] Mix 0.5 mol of erythromycin (template), monomer methacrylic acid (MAA), and cross-linking agent ethylene glycol dimethacrylate (EGDMA) according to the molar ratio of 1:3:20, and dissolve until 3ml Pore agent (acetonitrile: methanol = 3: 2), placed in an ampoule, then added 0.02 g of initiator azobisisobutyronitrile (AIBN), ultrasonicated for 10 minutes, then flushed with nitrogen for 5 minutes, vacuum sealed, 65 °C water bath for 24 hours to obtain the molecularly imprinted polymer of erythromycin. Take out the blocky polymer, grind it with a mortar, sieve it to a particle size of about 30-60 μm, suspend it with acetone and discard the fine particles. After the polymer was dried, the template was removed by Soxhlet extraction with methanol (containing 10% acetic acid) for 24 hours. After the elution was complete as determined by HPLC, it was dried at 60° C. for 24 hours for later use.
[0040] ...
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