Mechanisms underlying molecularly imprinted polymer molecular memory and the role of crosslinker: resolving debate on the nature of template recognition in phenylalanine anilide imprinted polymers

2012 ◽  
Vol 25 (2) ◽  
pp. 69-73 ◽  
Author(s):  
Gustaf D. Olsson ◽  
Björn C. G. Karlsson ◽  
Siamak Shoravi ◽  
Jesper G. Wiklander ◽  
Ian A. Nicholls
Keyword(s):  
Molecularly Imprinted Polymer ◽  
Molecular Memory ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Imprinted Polymers

Cyromazine imprinted polymers for selective stir bar sorptive extraction of melamine in animal feed and milk samples

The Analyst ◽  
2015 ◽  
Vol 140 (12) ◽  
pp. 4057-4067 ◽  
Author(s):  
Wenying Fan ◽  
Mingqi Gao ◽  
Man He ◽  
Beibei Chen ◽  
Bin Hu
Keyword(s):  
Molecularly Imprinted Polymer ◽  
Animal Feed ◽  
Stir Bar Sorptive Extraction ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Imprinted Polymers ◽  
Milk Samples ◽  
Sorptive Extraction ◽  
Dummy Template

A molecularly imprinted polymer coated stir bar was prepared using a self-designed polytetrafluoroethylene mold andin situpolymerization, with cyromazine as dummy template for target melamine.

Cationic pTyr/pSer imprinted polymers based on a bis-imidazolium host monomer: phosphopeptide recognition in aqueous buffers demonstrated by μ-liquid chromatography and monolithic columns

2017 ◽  
Vol 5 (5) ◽  
pp. 953-960 ◽  
Author(s):  
Celina Wierzbicka ◽  
Mingquan Liu ◽  
David Bauer ◽  
Knut Irgum ◽  
Börje Sellergren
Keyword(s):  
Liquid Chromatography ◽  
Polymer Films ◽  
Molecularly Imprinted Polymer ◽  
Monolithic Columns ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Imprinted Polymers ◽  
Phosphorylated Peptides

Capillary monoliths featuring grafted molecularly imprinted polymer films incorporating on a bis-imidazolium host monomer, displayed a remarkable crossreactivity with phosphorylated peptides in buffered media.

Recent developments in molecularly imprinted polymer nanofibers and their applications

2015 ◽  
Vol 7 (18) ◽  
pp. 7406-7415 ◽  
Author(s):  
Shabi Abbas Zaidi
Keyword(s):  
Molecularly Imprinted Polymer ◽  
Molecularly Imprinted Polymers ◽  
Imprinted Polymer ◽  
Polymer Nanofibers ◽  
Molecularly Imprinted ◽  
Imprinted Polymers ◽  
Recent Developments ◽  
Analyte Detection

Molecularly imprinted polymers (MIPs) have been potential and versatile candidates for analyte detection.

Synthesis of a novel cross-linker doubles as a functional monomer for preparing a water compatible molecularly imprinted polymer

2014 ◽  
Vol 6 (23) ◽  
pp. 9483-9489 ◽  
Author(s):  
Xiao Zhang ◽  
Feng Shen ◽  
Zhe Zhang ◽  
Yue Xing ◽  
Xueqin Ren
Keyword(s):  
Molecularly Imprinted Polymer ◽  
Naproxen Sodium ◽  
Functional Monomer ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Imprinted Polymers ◽  
Bifunctional Monomer ◽  
Cross Linker

A new bifunctional monomer acting as both a cross-linker and a functional monomer was synthesized and applied in the preparation of water-compatible naproxen sodium imprinted polymers.

Application of ratiometric fluorescence sensor-based microwave-assisted synthesized CdTe quantum dots and mesoporous structured epitope-imprinted polymers for highly efficient determination of tyrosine phosphopeptide

2020 ◽  
Vol 12 (1) ◽  
pp. 63-72 ◽  
Author(s):  
Nasibeh Saeedzadeh Amiri ◽  
Mohammad-Reza Milani Hosseini
Keyword(s):  
Quantum Dots ◽  
Molecularly Imprinted Polymer ◽  
Ratiometric Fluorescence ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Imprinted Polymers ◽  
Microwave Assisted ◽  
Silica Materials ◽  
Fluorescence Methods

Molecularly imprinted polymer coated quantum dot sensor modified with ratiometric fluorescence methods and mesoporous structured epitope imprinted silica materials (QDs@SiO2@EMSiO2) have been fabricated for detection of tyrosine phosphopeptide.

scholarly journals Reusable molecularly imprinted polymeric nanospheres for diclofenac removal from water samples

2020 ◽  
pp. 174751982092599
Author(s):  
Noha Amaly ◽  
Georges Istamboulie ◽  
Ahmed Y El-Moghazy ◽  
Thierry Noguer
Keyword(s):  
Molecularly Imprinted Polymer ◽  
Molecularly Imprinted Polymers ◽  
Water Samples ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Imprinted Polymers ◽  
Residue Removal ◽  
Pharmaceutical Pollutants ◽  
Polymer Nanospheres ◽  
Average Size

The preparation of efficient molecularly imprinted polymers materials (MIPs) for pharmaceutical residue removal is still a challenging task. Herein, we design uniformly molecularly imprinted polymer nanospheres via a precipitation polymerization method using methacrylic acid (MAA) as functional monomer and N,N-methylenebis(acrylamide) (MBAA) as a crosslinker for removal of diclofenac (DFC) as a model for pharmaceutical pollutants. Nanospheres with average size 200 nm were prepared with MAA:MBAA at a ratio of 1:7 and acetonitrile/toluene (1:1) as a porogenic solvent. The successful synthesis is evidenced by Fourier transform infrared spectroscopy, scanning electron microscopy, and with a particle size analyzer. The rebinding experiments confirmed that the more introduction of the carboxyl groups from MAA could remarkably improve the imprinting effect with a significantly increased imprinting factor and specific rebinding capacity reached 450 mg/g after 15 min. Furthermore, the adsorption capacity of the molecularly imprinted polymers is maintained above 85% after seven regeneration cycles, indicating that the molecularly imprinted polymers can be used multiple times. Moreover, the developed molecularly imprinted polymers show promising DFC removal efficiency from real water samples, which suggests that the prepared molecularly imprinted polymer nanospheres are promising in DFC separation.

Molecularly Imprinted Polymer and Computational Study of (E)-4-(2- cyano-3-(dimethylamino)acryloyl)benzoic Acid from Poly(ethylene terephthalate) Plastic Waste

2020 ◽  
Vol 16 (2) ◽  
pp. 119-137 ◽  
Author(s):  
Asmaa M. Fahim ◽  
Bartłomiej Wasiniak ◽  
Jerzy P. Łukaszewicz
Keyword(s):  
Benzoic Acid ◽  
Molecularly Imprinted Polymer ◽  
Molecularly Imprinted Polymers ◽  
Ethylene Terephthalate ◽  
Computational Study ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Imprinted Polymers ◽  
Poly Ethylene Terephthalate ◽  
Poly Ethylene

Background: Molecularly imprinted polymers (MIPs) are utilized in the separation of a pure compound from complex matrices. A stable template-monomer complex generates MIPs with the highest affinity and selectivity for the template. In this investigation, degradation of Poly(ethylene terephthalate) PET afforded the (E)-4-(2-cyano-3-(dimethylamino) acryloyl) benzoic acid (4) (TAM) which used TAM as template which interacts with Methacrylic Acid (MAA) monomer, in the presence of CH3CN as progen. The TAM-MMA complex interactions are dependent on stable hydrogen bonding interaction between the carboxylic acid group of TAM and the hydroxyl group of MMA with minimal interference of porogen CH3CN. The DFT/B3LYP/6-31+G model chemistry was used to optimize their structures and frequency calculations. The binding energies between TAM with different monomers showed the most stable molar ratio of 1:4 which was confirmed through experimental analysis. Methods: The present work describes the synthesis of (E)-4-(2-cyano-3-(dimethylamino) acryloyl) benzoic acid (4) (TAM) from PET waste and formation of molecularly imprinted polymer from TAM with the methacrylic acid monomer. The optimization of molecular imprinted was stimulated via DFT/B3LYP/6-31G (d). The imprinted polymer film was characterized via thermal analysis, pore size, FT-IR and scanning electron microscopy. Results: The most stable molecularly imprinted polymers (MIPs) showed binding energy of TAM(MMA4)=-2063.456 KJ/mol with a small value of mesopores (10-100 Å). Also, the sorption capability of TAM-MIPs showed 6.57 mg/g using STP-MIP-9VC. Moreover, the average pore size ranged between 0.2-1 nm with the BET surface about 300 m2/g. Conclusion: The proposed TAM exhibited a high degree of selectivity for MMA in comparison with other different monomers through hydrogen bond interaction, which was thermally stable, good reproducibility and excellent regeneration capacity and elucidated in the computational study and analytical analysis.

Synthesis and Evaluation of a Molecularly Imprinted Polymer Selective to 2,4,6-Trichlorophenol

2004 ◽  
Vol 57 (8) ◽  
pp. 759 ◽  
Author(s):  
Lachlan Schwarz ◽  
Clovia I. Holdsworth ◽  
Adam McCluskey ◽  
Michael C. Bowyer
Keyword(s):  
Molecularly Imprinted Polymer ◽  
Molecularly Imprinted Polymers ◽  
Competitive Binding ◽  
Imprinted Polymer ◽  
Binding Studies ◽  
Molecularly Imprinted ◽  
Imprinted Polymers ◽  
Target Molecule ◽  
High Preference ◽  
Structural Analogues

Molecularly imprinted polymers (MIPs) selective for the phenolic contaminant 2,4,6-trichlorophenol (2,4,6-TCP) were prepared and evaluated in three porogens of differing character (hexane, acetonitrile, dichloromethane). Rebinding of 2,4,6-TCP was found to be most effective in dichloromethane (imprinting factor: 13.2). Competitive binding studies performed against a range of close structural analogues showed a high preference for the target molecule, although partial recognition towards 2,4-dichlorophenol was also observed. Specificity was found to be dependent upon the presence of ring chlorine on the target, which suggested that these atoms participate in secondary binding interactions that are essential for successful recognition in the polymer cavity.

Boronate-affinity hollow molecularly imprinted polymers for the selective extraction of nucleosides

2017 ◽  
Vol 41 (15) ◽  
pp. 7133-7141 ◽  
Author(s):  
Yue Hu ◽  
Wei Huang ◽  
Yukui Tong ◽  
Qinfei Xia ◽  
Miaomiao Tian
Keyword(s):  
Molecularly Imprinted Polymer ◽  
Molecularly Imprinted Polymers ◽  
Selective Extraction ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Imprinted Polymers ◽  
Selective Enrichment

Preparation of a boronate-affinity hollow molecularly imprinted polymer and its application as an SPE adsorbent for the selective enrichment of nucleosides.

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