Method for preparing 17beta-estradiol molecularly imprinted polymer by adopting mixed template
A technology of mixed templates and molecular imprinting, applied in chemical instruments and methods, other chemical processes, etc., can solve the problem of polymers without high affinity, achieve the effects of shortening detection time, reducing detection cost, and broad application prospects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0022] In a 100ml medical saline bottle, dissolve 0.1mmol of 17α-estradiol and 0.1mmol of 17β-estradiol in 3ml of acetonitrile, then add 1mmol of methyl methacrylate (MA) to the acetonitrile, ultrasonically treat for 3min and mix well Add 1 mmol of ethylene glycol dimethacrylate (EGDMA), ultrasonically treat it for 3 min to make it evenly mixed, then let stand for 1 h at room temperature, add 20 mg of initiator azobisisobutyronitrile after standing, and then pass N 2 After 5 minutes, it was quickly sealed. After sealing, it was reacted in a water bath shaker at 50 °C for 36 hours. After the reaction was completed, a blocky polymer was generated. The particles are eluted with a mixture of 100 ml methanol and acetic acid by Soxhlet extraction, and the template molecules are removed until the eluent does not contain template molecules, and the volume fraction of acetic acid in the mixture is 10%. Soxhlet extraction The conditions of extraction were 5 times of extraction for 8 hou...
Embodiment 2
[0024] In a 100ml medical saline bottle, dissolve 0.1mmol of 17α-estradiol and 0.15mmol of 17β-estradiol in 5ml of acetonitrile, add 1mmol of methacrylic acid (MAA) to the acetonitrile, and then add 1mmol of 1mmol after sonicating for 3min and mixing evenly EGDMA, ultrasonically treated for 4 min to make it evenly mixed, then allowed to stand at room temperature for 1 h, after standing, add 20 mg of initiator azobisisobutyronitrile, and then pass N 2 After 10 minutes, it was quickly sealed. After sealing, it was reacted in a water bath shaker at 55°C for 32 hours. After the reaction was completed, a blocky polymer was generated. The particles are eluted with a mixture of 100 ml methanol and acetic acid by Soxhlet extraction, and the template molecules are removed until the eluent does not contain template molecules, and the volume fraction of acetic acid in the mixture is 10%. Soxhlet extraction The conditions of extraction were 4 times of extraction for 10 hours each time, an...
Embodiment 3
[0026] In a 100ml medical saline bottle, dissolve 0.2mmol of 17α-estradiol and 0.1mmol of 17β-estradiol in 5ml of chloroform, then add 1mmol of MAA to the chloroform, ultrasonically treat for 3min and mix well, add 1mmol of EGDMA, and ultrasonically treat for 5min Make it evenly mixed, then stand at room temperature for 1h, add 25mg initiator azobisisobutyronitrile after standing, and then pass N 2 After 8 minutes, it was quickly sealed. After sealing, it was reacted in a water bath shaker at 65°C for 16 hours. After the reaction was completed, a blocky polymer was generated. The particles are eluted with a mixture of 100 ml methanol and acetic acid by Soxhlet extraction, and the template molecules are removed until the eluent does not contain template molecules, and the volume fraction of acetic acid in the mixture is 10%. Soxhlet extraction The conditions of extraction were 3 times of extraction for 12 hours each time, and finally eluted with methanol twice to remove acetic ...
PUM
Property | Measurement | Unit |
---|---|---|
particle diameter | aaaaa | aaaaa |
adsorption capacity | aaaaa | aaaaa |
adsorption capacity | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com