scholarly journals The Use of Computational Methods for the Development of Molecularly Imprinted Polymers

Polymers ◽  
2021 ◽  
Vol 13 (17) ◽  
pp. 2841
Author(s):  
Ian A. Nicholls ◽  
Kerstin Golker ◽  
Gustaf D. Olsson ◽  
Subramanian Suriyanarayanan ◽  
Jesper G. Wiklander

Recent years have witnessed a dramatic increase in the use of theoretical and computational approaches in the study and development of molecular imprinting systems. These tools are being used to either improve understanding of the mechanisms underlying the function of molecular imprinting systems or for the design of new systems. Here, we present an overview of the literature describing the application of theoretical and computational techniques to the different stages of the molecular imprinting process (pre-polymerization mixture, polymerization process and ligand–molecularly imprinted polymer rebinding), along with an analysis of trends within and the current status of this aspect of the molecular imprinting field.

2021 ◽  
Vol 9 (3) ◽  
Author(s):  
Jozef Lehotay ◽  
Miroslava Lachová ◽  
Ján Mocák

Molecularly imprinted polymers were prepared and tested in different way. 1-methyl-2-piperidinoethylester of 4-decyloxyphenylcarbamic acid was used as template for imprints formation. Acrylamide, 4-vinylpyridine and methacrylic acid as monomers and methanol and acetonitrile as a porogene were used. Non-imprinted polymers (NIP) were prepared for each imprinted polymer by the same procedure. Polymers were employed as sorbents for solid-phase extraction (SPE). In this work the influence of polymerization mixture composition on polymer properties, such as capacity and selectivity, was investigated. The influence of alkoxy-chain length and position on benzene ring on the selectivity of polymers was also investigated.


2003 ◽  
Vol 21 (3) ◽  
pp. 261-268 ◽  
Author(s):  
K. Sreenivasan ◽  
R. Sivakumar

Molecular imprinting is an elegant approach to the synthesis of polymers with predetermined recognition properties, the technique of molecular imprinting involving arranging the functional monomers around the print molecules prior to polymerisation. Molecularly imprinted polymers (MIPs) show a remarkable ability to bind print molecule from a mixture of entities which are close in structure. One of the serious drawbacks of MIPs is their low adsorption capacity and one approach to improving this relies on the use of chemically modified monomers in the synthesis of the MIPs. This report discusses the synthesis and evaluation of an MIP based on ferric acrylate as an adsorbent for cholesterol.


Molecules ◽  
2021 ◽  
Vol 26 (18) ◽  
pp. 5612
Author(s):  
Aliya Nur Hasanah ◽  
Nisa Safitri ◽  
Aulia Zulfa ◽  
Neli Neli ◽  
Driyanti Rahayu

Molecular imprinting is a technique for creating artificial recognition sites on polymer matrices that complement the template in terms of size, shape, and spatial arrangement of functional groups. The main advantage of Molecularly Imprinted Polymers (MIP) as the polymer for use with a molecular imprinting technique is that they have high selectivity and affinity for the target molecules used in the molding process. The components of a Molecularly Imprinted Polymer are template, functional monomer, cross-linker, solvent, and initiator. Many things determine the success of a Molecularly Imprinted Polymer, but the Molecularly Imprinted Polymer component and the interaction between template-monomers are the most critical factors. This review will discuss how to find the interaction between template and monomer in Molecularly Imprinted Polymer before polymerization and after polymerization and choose the suitable component for MIP development. Computer simulation, UV-Vis spectroscopy, Fourier Transform Infrared Spectroscopy (FTIR), Proton-Nuclear Magnetic Resonance (1H-NMR) are generally used to determine the type and strength of intermolecular interaction on pre-polymerization stage. In turn, Suspended State Saturation Transfer Difference High Resolution/Magic Angle Spinning (STD HR/MAS) NMR, Raman Spectroscopy, and Surface-Enhanced Raman Scattering (SERS) and Fluorescence Spectroscopy are used to detect chemical interaction after polymerization. Hydrogen bonding is the type of interaction that is becoming a focus to find on all methods as this interaction strongly contributes to the affinity of molecularly imprinted polymers (MIPs).


2017 ◽  
Author(s):  
◽  
Jingjing Dai

Molecularly imprinted polymers are specialty polymers with ability of selectively capturing target molecules. They show great potential to be environmental sensors for the detection of specific contaminant. The overall research objective is to investigate the sensing ability of MIPs based on two mechanisms fluorescence quenching and reflectance for two example contaminants 2, 4-dinitrotoluene and 2-butoxylethanol, which are fingerprinting contaminant of explosive manufacturing and hydraulic fracking. The water chemistry effects are explored on MIPs for their potential use as in-situ sensors in complex aquatic environments. Fluorescent carbon dots with different surface functionality were fabricated and their environmental fate was explored. Amino-functionalized carbon dots (AC-dots) were applied to fluorescently label a molecularly imprinted polymer (MIP) for 2, 4-dinitrotoluene (DNT) as a template. DNT is specifically captured by the cavities in the MIP and interact with AC-dots on the surface, resulting in quenching of the fluorescence of the AC-dots. Response to DNT reaches equilibrium within [about]30 min. The method has a dynamic range that extends from 1 to 15 ppm, and allows for quantitation of DNT in aqueous solutions, with a detection limit of 0.28 ppm. Selectivity tests conducted in presence of DNT analogs demonstrated the specific recognition of DNT. The effect of sample water chemistry on carbon dots labeled molecularly imprinted polymer (AC-MIP) sensor the detection of 2, 4-dinitrotoluene (DNT) was investigated. With the increase of ionic strength from 1 mM to 100 mM, the quenching amount of MIPs decreased about 19% and 30% with NaCl and CaCl2 respectively. In the range of pH from 4 to 9, quenching effect is slightly higher at basic environment for both MIPs and non-imprinted polymers (NIPs) resulting from swelling properties of the films. NOM added the quenching amount to the sensor with a modified equation developed with NOM as a variable. In both lake water and tap water, DNT concentrations read by the sensors were very close to the HPLC measured DNT concentrations with the range from 72% to 105%. Molecularly imprinted polymers (MIPs) sensors for detection of 2-butoxyethanol (2BE), a pollutant associated with hydraulic fracturing contamination, were developed based on the combination of a colloidal crystal templating method and a molecular imprinting technique. MIPs exhibited higher binding than non-imprinted films (NIPs) due to the specific adsorption provided by molecular imprinting with imprinting efficiencies around 2. Optical tests were performed because of the uniformly ordered porous structure. The reflectance spectra of the sensors showed Bragg's peaks, which responded to the presence of 2BE; peaks presented increasing red shifts up to 50 nm with 2BE concentrations in the range of 1 ppb to 100 ppm, which allowed quantitative estimates of present 2BE concentration in aqueous solutions. The material has the potential for early detection of hydraulic fracturing sites contamination.


2016 ◽  
Vol 4 (44) ◽  
pp. 7138-7145 ◽  
Author(s):  
Hirobumi Sunayama ◽  
Takeo Ohta ◽  
Atsushi Kuwahara ◽  
Toshifumi Takeuchi

An antibiotic-imprinted cavity with two different fluorescent dyes was prepared by molecular imprinting and subsequent post-imprinting modifications (PIMs), for the readout of a specific binding event as a fluorescence signal.


2015 ◽  
Vol 7 (18) ◽  
pp. 7406-7415 ◽  
Author(s):  
Shabi Abbas Zaidi

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


2018 ◽  
Vol 42 (19) ◽  
pp. 16144-16153 ◽  
Author(s):  
Arash Asfaram ◽  
Maryam Arabi ◽  
Abbas Ostovan ◽  
Hossein Sadeghi ◽  
Mehrorang Ghaedi

In the present study, a D-μ-SPE clean-up method was established for the analysis of quercetin in extracts of plants and food samples using a magnetic molecularly imprinted polymer as the sorbent by HPLC-UV detection.


2005 ◽  
Vol 30 (4) ◽  
pp. 67-73 ◽  
Author(s):  
Chin-Yin Hung ◽  
Han-Hung Huang ◽  
Ching-Chiang Hwang

Styrene is used in a variety of chemical industries. Environmental and occupational exposures to styrene occur predominantly through inhalation. The major metabolite of styrene is present in two enantiomeric forms, chiral R- and S- hydroxy-1-phenyl-acetic acid (R-and S-mandelic acid, MA). Thus, the concentration of MA, particularly of its enantiomers, has been used in urine tests to determine whether workers have been exposed to styrene. This study describes a method of analyzing mandelic acid using molecular imprinting techniques and HPLC detection to perform the separation of diastereoisomers of mandelic acid. The molecularly imprinted polymer (MIP) was prepared by non-covalent molecular imprinting using (+) MA, (-) MA or (+) phenylalanine, (-) phenylalanine as templates. Methacrylic acid (MAA) and ethylene glycol dimethacrylate (EGDMA) were copolymerized in the presence of the template molecules. The bulk polymerization was carried out at 4ºC under UV radiation. The resulting MIP was grounded into 25~44¼m particles, which were slurry packed into analytical columns. After the template molecules were removed, the MIP-packed columns were found to be effective for the chromatographic resolution of (±)-mandelic acid. This method is simpler and more convenient than other chromatographic methods.


RSC Advances ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 5394-5401 ◽  
Author(s):  
Wei Huang ◽  
Xingyu Hou ◽  
Yukui Tong ◽  
Miaomiao Tian

Boronate-affinity magnetic hollow molecularly imprinted polymers were prepared with sialic acid (SA) as a template to selectively extract SA from serum samples coupled with HPLC-UV.


2020 ◽  
pp. 174751982092599
Author(s):  
Noha Amaly ◽  
Georges Istamboulie ◽  
Ahmed Y El-Moghazy ◽  
Thierry Noguer

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.


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