Polymers

Research

Jump to: Review

12 pages, 711 KiB

Open AccessArticle

New Methods to Study the Behavior of Molecularly Imprinted Polymers in Aprotic Solvents

by Anett Nagy-Szakolczai, Zsanett Dorkó, Blanka Tóth and George Horvai

Polymers 2018, 10(9), 1015; https://doi.org/10.3390/polym10091015 - 12 Sep 2018

Cited by 7 | Viewed by 3336

Abstract

This work presents three new experimental methods for studying molecular imprinting. The electric conductivity measurements of the pre-polymerization mixture of amine templates in an aprotic solvent provide evidence of ionic dissociation of the pre-polymerization complexes. The displacement measurement of the template propranolol from [...] Read more.

This work presents three new experimental methods for studying molecular imprinting. The electric conductivity measurements of the pre-polymerization mixture of amine templates in an aprotic solvent provide evidence of ionic dissociation of the pre-polymerization complexes. The displacement measurement of the template propranolol from its molecularly imprinted polymer (MIP) using a quaternary ammonium ion in toluene, shows that this MIP behaves as an ion exchanger even in a non-polar solvent. The same experiment also shows that template binding to the MIP from toluene involves ionic interaction. The third experimental method introduced here serves to study the models of template binding on MIPs. To this end the binding isotherm of propranolol (PR) has been measured on a polymer mixture consisting of non-imprinted control polymer (NIP) and a stronger binding acidic polymer, respectively. All three methods are suitable for studying several other imprinting systems. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Figure 1

20 pages, 6625 KiB

Open AccessArticle

Pressure-Stable Imprinted Polymers for Waste Water Remediation

by Shane Mann, Travis Johnson, Evie Medendorp, Robert Ocomen, Luke DeHart, Adam Bauer, Bingbing Li, Mary Tecklenburg and Anja Mueller

Polymers 2018, 10(7), 704; https://doi.org/10.3390/polym10070704 - 26 Jun 2018

Cited by 2 | Viewed by 3914

Abstract

In wastewater treatment, the removal of heavy metal ions is difficult. Ion exchange resins are ineffective since heavy metal ions cannot compete with “hard ions” in binding to the resins. Imprinting polymerization can increase the specificity of ion exchange resins to allow heavy [...] Read more.

In wastewater treatment, the removal of heavy metal ions is difficult. Ion exchange resins are ineffective since heavy metal ions cannot compete with “hard ions” in binding to the resins. Imprinting polymerization can increase the specificity of ion exchange resins to allow heavy metal ions to compete. Unfortunately, a high capacity is also needed. When high porosity and surface area are used to increase capacity, polymeric resins lose pressure stability needed for water treatment. In this research, a bulky, hydrophobic co-monomer was used to prevent Zn⁺² imprinted sites from collapsing. Both the co-monomer and crosslinking density were optimized to allow for maximum pore access while maintaining pressure stability. IR and SEM studies were used to study phase separation of the hydrophobic co-monomer from the hydrophilic resin. Capacity was measured for just the imprinting ion first, and then in combination with a competing ion and compared with porosity and pore-size measurements. Capacity under pressure was also characterized. A resin with high capacity was identified that allowed for the heavy metal ion to compete while still maintaining pressure stability. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Figure 1

16 pages, 10229 KiB

Open AccessArticle

Molecularly Imprinted Polymers for the Selective Extraction of Bisphenol A and Progesterone from Aqueous Media

by César Cáceres, Catalina Bravo, Bernabé Rivas, Ewa Moczko, Pedro Sáez, Yadiris García and Eduardo Pereira

Polymers 2018, 10(6), 679; https://doi.org/10.3390/polym10060679 - 19 Jun 2018

Cited by 25 | Viewed by 5284

Abstract

This paper describes the development of a novel sorbent for selective extraction of endocrine disruptors (EDs) from aqueous media. The main goal was to obtain sufficient molecularly imprinted polymers (MIPs) for selective detection, preconcentration, and extraction of EDs such as bisphenol A (BPA) [...] Read more.

This paper describes the development of a novel sorbent for selective extraction of endocrine disruptors (EDs) from aqueous media. The main goal was to obtain sufficient molecularly imprinted polymers (MIPs) for selective detection, preconcentration, and extraction of EDs such as bisphenol A (BPA) and progesterone (PG). Series of MIPs and their analogues, non-molecularly imprinted polymers (NIPs), were synthesised following a non-covalent imprinting strategy based on radical polymerisation. Sets of synthesis were performed in order to optimise variables of the polymerisation including solvent, cross-linker, and template ratio. The retention capacity of MIPs was determined using HPLC in the range of 33.3% to 96.6% and 32.5% to 96% for BPA and PG, respectively. The adsorption mechanism was studied by isothermal and kinetic assays. The kinetic analysis showed a high retention capacity within 15 min of contact. The polymer yield was obtained in the range of 30% to 100%. Additionally, there was no significant cross-reactivity observed upon testing MIPs with structural analogues and other endocrine disruptors instead of target molecules. The results also revealed the high importance of different concentrations of cross-linker and solvent during the polymerisation. Firstly, the pre-organisation of complementary functional groups, which were present in the polymerisation mixture, and secondly, selective cavity formation for target molecules. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Graphical abstract

13 pages, 3520 KiB

Open AccessArticle

Photonic Molecularly Imprinted Polymer Film for the Detection of Testosterone in Aqueous Samples

by Abbas J. Kadhem, Shuting Xiang, Susan Nagel, Chung-Ho Lin and Maria Fidalgo de Cortalezzi

Polymers 2018, 10(4), 349; https://doi.org/10.3390/polym10040349 - 22 Mar 2018

Cited by 28 | Viewed by 6040

Abstract

The detection of testosterone in aqueous solutions is a difficult task due to the low concentration levels that are relevant in environmental and physiological samples. Current analytical methods are expensive and/or complex. To address this issue, we fabricated a molecularly imprinted polymer (MIP) [...] Read more.

The detection of testosterone in aqueous solutions is a difficult task due to the low concentration levels that are relevant in environmental and physiological samples. Current analytical methods are expensive and/or complex. To address this issue, we fabricated a molecularly imprinted polymer (MIP) photonic film for the detection of testosterone in water. The films were obtained using colloidal crystals as templates for the pore morphology. Monodispersed silica particles with an average diameter 330 nm were used to obtain the colloidal crystal by vertical deposition. A solution of acrylic acid with testosterone as the imprinted template was infiltrated in the colloidal crystal and polymerized via bulk polymerization; the particles were then removed by acid etching and the testosterone eluted by a suitable solvent. The material was characterized by FTIR, swelling experiments and microscopy; MIPs were investigated by equilibrium rebinding, kinetics and reuse experiments. The results showed that the MIPs exhibited selectivity to the template, a 30-min equilibration time and stability after at least six cycles of use and regeneration. After incubation, the reflectance spectra of the films showed a shift of the Bragg diffraction peak that correlated with testosterone concentration in the 5–100 ppb range. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Graphical abstract

14 pages, 11909 KiB

Open AccessArticle

Preparation of Molecularly Imprinted Mesoporous Materials for Highly Enhancing Adsorption Performance of Cytochrome C

by Zhiling Li, Ping Guan, Xiaoling Hu, Shichao Ding, Yuan Tian, Yarong Xu and Liwei Qian

Polymers 2018, 10(3), 298; https://doi.org/10.3390/polym10030298 - 10 Mar 2018

Cited by 25 | Viewed by 4831

Abstract

Molecularly imprinted mesoporous materials (MIMs) were synthesized to improve the adsorption performance of Cytochrome c (Cyt c) by using an imidazolium-based amphiphilic ionic liquid 1-octadecyl-3-methylimidazolium chloride (C₁₈MIMCl) as surfactant in aqueous solution via the epitope imprinting approach. The surface-exposed C-terminus nonapeptide [...] Read more.

Molecularly imprinted mesoporous materials (MIMs) were synthesized to improve the adsorption performance of Cytochrome c (Cyt c) by using an imidazolium-based amphiphilic ionic liquid 1-octadecyl-3-methylimidazolium chloride (C₁₈MIMCl) as surfactant in aqueous solution via the epitope imprinting approach. The surface-exposed C-terminus nonapeptide of Cyt c (residues 96–104, AYLKKATNE) was utilized as the imprinted template. The nitrogen adsorption-desorption, thermo-gravimetric analysis, and transmission electron microscopy verified the successful preparation of MIMs with ordered mesoporous structure. The adsorption isotherm studies showed that the obtained MIMs exhibited superior adsorption capacity toward Cyt c of 86.47 mg·g⁻¹ because of the high specific surface areas of 824 m²·g⁻¹, and the appropriate pore size promoted the mass transfer of Cyt c, causing a rapid adsorption equilibrium within 20 min. Furthermore, these MIMs still remained excellent selectivity and recognition ability according to the selective as well as the competitive adsorption studies, suggesting that the molecularly imprinted mesoporous materials is expected to be used in the field of highly efficient separation and enrichment of proteins. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Graphical abstract

9 pages, 2092 KiB

Open AccessArticle

Affinity Capillary Electrochromatography of Molecularly Imprinted Thin Layers Grafted onto Silica Capillaries Using a Surface-Bound Azo-Initiator and Living Polymerization

by Cristina Giovannoli, Cinzia Passini, Fabio Di Nardo, Laura Anfossi, Claudio Baggiani and Ian A. Nicholls

Polymers 2018, 10(2), 192; https://doi.org/10.3390/polym10020192 - 15 Feb 2018

Cited by 12 | Viewed by 3429

Abstract

Molecularly imprinted thin layers were prepared in silica capillaries by using two different surface polymerization strategies, the first using 4,4′-azobis(4-cyanovaleric acid) as a surface-coupled radical initiator, and the second, S-carboxypropyl-S’-benzyltrithiocarbonate as a reversible addition-fragmentation chain transfer (RAFT) agent in combination with 2,2′-azobisisobutyronitrile as [...] Read more.

Molecularly imprinted thin layers were prepared in silica capillaries by using two different surface polymerization strategies, the first using 4,4′-azobis(4-cyanovaleric acid) as a surface-coupled radical initiator, and the second, S-carboxypropyl-S’-benzyltrithiocarbonate as a reversible addition-fragmentation chain transfer (RAFT) agent in combination with 2,2′-azobisisobutyronitrile as a free radical initiator. The ability to generate imprinted thin layers was tested on two different polymerization systems: (i) a 4-vinylpyridine/ethylene dimethacrylate (4VP-EDMA) in methanol-water solution with 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) as a template; and (ii) methacrylic acid/ethylene dimethacrylate (MAA-EDMA) in a chloroform solution with warfarin as the template molecule. The binding properties of the imprinted capillaries were studied and compared with those of the corresponding non-imprinted polymer coated capillaries by injecting the template molecule and by measuring its migration times relative to a neutral and non-retained marker. The role of running buffer hydrophobicity on recognition was investigated by studying the influence of varying buffer acetonitrile concentration. The 2,4,5-T-imprinted capillary showed molecular recognition based on a reversed phase mechanism, with a decrease of the template recognition in the presence of higher acetonitrile content; whereas warfarin-imprinted capillaries showed a bell-shaped trend upon varying the acetonitrile percentage, illustrating different mechanisms underlying imprinted polymer-ligand recognition. Importantly, the results demonstrated the validity of affinity capillary electrochromatography (CEC) to screen the binding properties of imprinted layers. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Graphical abstract

14 pages, 7479 KiB

Open AccessArticle

Preparation of Protein Molecular-Imprinted Polysiloxane Membrane Using Calcium Alginate Film as Matrix and Its Application for Cell Culture

by Dong Liu, Kongyin Zhao, Meng Qi, Shuwen Li, Guoqing Xu, Junfu Wei and Xiaoling He

Polymers 2018, 10(2), 170; https://doi.org/10.3390/polym10020170 - 10 Feb 2018

Cited by 25 | Viewed by 5068

Abstract

Bovine serum albumin (BSA) molecular-imprinted polysiloxane (MIP) membrane was prepared by sol-gel technology, using silanes as the functional monomers, BSA as the template and CaAlg hydrogel film as the matrix. The stress-strain curves of wet CaAlg membrane and molecular-imprinted polysiloxane membrane were investigated. [...] Read more.

Bovine serum albumin (BSA) molecular-imprinted polysiloxane (MIP) membrane was prepared by sol-gel technology, using silanes as the functional monomers, BSA as the template and CaAlg hydrogel film as the matrix. The stress-strain curves of wet CaAlg membrane and molecular-imprinted polysiloxane membrane were investigated. We evaluate the adsorption and recognition properties of MIP membrane. Results showed that the adsorption capacity of BSA-imprinted polysiloxane for BSA reached 28.83 mg/g, which was 2.18 times the non-imprinted polysiloxane (NIP) membrane. The adsorption rate was higher than that of the protein-imprinted hydrogel. BSA-imprinted polysiloxane membrane could identify the protein template from competitive proteins such as bovine hemoglobin, ovalbumin and bovine γ-globulin. In order to obtain the biomaterial that can promote cell adhesion and proliferation, fibronectin (FN)-imprinted polysiloxane (FN-MIP) membrane was obtained by using fibronectin as the template, silanes as functional monomers, and CaAlg hydrogel membrane as the substrate or matrix. The FN-MIP adsorbed more FN than NIP. The FN-imprinted polysiloxane membrane was applied to culture mouse fibroblast cells (L929) and the results proved that the FN-MIP had a better effect on cell adhesion than NIP. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Figure 1

11 pages, 3767 KiB

Open AccessArticle

Synthesis of Molecularly Imprinted Cryogels to Deplete Abundant Proteins from Bovine Serum

by Chun Yang, Yan Zhang, Wei-Qin Cao, Xiao-Feng Ji, Jian Wang, Ya-Nan Yan, Tao-Lin Zhong and Yu Wang

Polymers 2018, 10(1), 97; https://doi.org/10.3390/polym10010097 - 20 Jan 2018

Cited by 14 | Viewed by 4486

Abstract

Molecularly imprinted polyacrylamide cryogels were synthesized with pending templates (bovine serums of different concentrations). As the serum concentrations increased in the monomer solutions, the resulting cryogels could adsorb and deplete more proteins from serum samples. Due to the addition of vinyltriethoxysilane (VTEOS) in [...] Read more.

Molecularly imprinted polyacrylamide cryogels were synthesized with pending templates (bovine serums of different concentrations). As the serum concentrations increased in the monomer solutions, the resulting cryogels could adsorb and deplete more proteins from serum samples. Due to the addition of vinyltriethoxysilane (VTEOS) in the prepolymerizing solutions, the polymers came as organic–inorganic hybrid materials. It endued the silica-modified amphoteric polyacrylamide cryogels with improved mechanical strengths. Scanning electron micrography (SEM), Infrared (IR) spectrometry, thermogravimetry-differential thermal analysis (TG-DTA), and X-ray photoelectron spectroscopy (XPS) were carried out to characterize these macroporous polymers. Amphoteric cryogels proved to be favorable materials recognizing and binding proteins. When used as liquid chromatography stationary phases, they were capable of simultaneously adsorbing various serum proteins. Electrophoresis showed that abundant proteins were gradually depleted by the cryogels prepared from increased ratios of bovine serums in the monomer solutions. As abundant proteins are always imprinted first, this sample per se imprinting method provides an effective and convenient way to deplete abundant proteins from complex samples such as serums, meanwhile concentrating and collecting scarce species therein. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Graphical abstract

3918 KiB

Open AccessArticle

The Multi-Template Molecularly Imprinted Polymer Based on SBA-15 for Selective Separation and Determination of Panax notoginseng Saponins Simultaneously in Biological Samples

by Chenghong Sun, Jinhua Wang, Jiaojiao Huang, Dandan Yao, Chong-Zhi Wang, Lei Zhang, Shuying Hou, Lina Chen and Chun-Su Yuan

Polymers 2017, 9(12), 653; https://doi.org/10.3390/polym9120653 - 28 Nov 2017

Cited by 16 | Viewed by 6437

Abstract

The feasible, reliable and selective multi-template molecularly imprinted polymers (MT-MIPs) based on SBA-15 (SBA-15@MT-MIPs) for the selective separation and determination of the trace level of ginsenoside Rb₁ (Rb₁), ginsenoside Rg₁ (Rg₁) and notoginsenoside R₁ (R₁ [...] Read more.

The feasible, reliable and selective multi-template molecularly imprinted polymers (MT-MIPs) based on SBA-15 (SBA-15@MT-MIPs) for the selective separation and determination of the trace level of ginsenoside Rb₁ (Rb₁), ginsenoside Rg₁ (Rg₁) and notoginsenoside R₁ (R₁) simultaneously from biological samples were developed. The polymers were constructed by SBA-15 as support, Rb₁, Rg₁, R₁ as multi-template, acrylamide (AM) as functional monomer and ethylene glycol dimethacrylate (EGDMA) as cross-linker. The new synthetic SBA-15@MT-MIPs were satisfactorily applied to solid-phase extraction (SPE) coupled with high performance liquid chromatography (HPLC) for the separation and determination of trace Rb₁, Rg₁ and R₁ in plasma samples. Under the optimized conditions, the limits of detection (LODs) and quantitation (LOQs) of the proposed method for Rb₁, Rg₁ and R₁ were in the range of 0.63–0.75 ng·mL⁻¹ and 2.1–2.5 ng·mL⁻¹, respectively. The recoveries of R₁, Rb₁ and Rg₁ were obtained between 93.4% and 104.3% with relative standard deviations (RSDs) in the range of 3.3–4.2%. All results show that the obtained SBA-15@MT-MIPs could be a promising prospect for the practical application in the selective separation and enrichment of trace Panax notoginseng saponins (PNS) in the biological samples. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Graphical abstract

3489 KiB

Open AccessArticle

Studying the Drug Delivery Kinetics of a Nanoporous Matrix Using a MIP-Based Thermal Sensing Platform

by Christopher J. Pawley, Ariane Perez-Gavilan, Kaelin S. Foley, Sarah Lentink, Hannah N. Welsh, Gabrielle Tuijthof, Erik Steen Redeker, Hanne Diliën, Kasper Eersels, Bart Van Grinsven and Thomas J. Cleij

Polymers 2017, 9(11), 560; https://doi.org/10.3390/polym9110560 - 28 Oct 2017

Cited by 5 | Viewed by 7135

Abstract

The implementation of Molecularly Imprinted Polymers (MIPs) into sensing systems has been demonstrated abundantly over the past few decades. In this article, a novel application for an MIP-based thermal sensing platform is introduced by using the sensor to characterize the drug release kinetics [...] Read more.

The implementation of Molecularly Imprinted Polymers (MIPs) into sensing systems has been demonstrated abundantly over the past few decades. In this article, a novel application for an MIP-based thermal sensing platform is introduced by using the sensor to characterize the drug release kinetics of a nanoporous silver-organic framework. This Ag nanoporous matrix was loaded with acetylsalicylic acid (aspirin) which was used as a model drug compound in this study. The drug elution properties were studied by placing the nanoporous matrix in phosphate buffered saline solution for two days and measuring the drug concentration at regular time intervals. To this extent, an acrylamide-based MIP was synthesized that was able to detect aspirin in a specific and selective manner. Rebinding of the template to the MIP was analyzed using a thermal sensor platform. The results illustrate that the addition of aspirin into the sensing chamber leads to a concentration-dependent increase in the phase shift of a thermal wave that propagates through the MIP-coated sensor chip. After constructing a dose-response curve, this system was used to study the drug release kinetics of the nanoporous matrix, clearly demonstrating that the metalorganic framework releases the drug steadily over the course of the first hour, after which the concentration reaches a plateau. These findings were further confirmed by UV–Visible spectroscopy, illustrating a similar time-dependent release in the same concentration range, which demonstrates that the MIP-based platform can indeed be used as a low-cost straightforward tool to assess the efficacy of drug delivery systems in a lab environment. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Figure 1

Review

Jump to: Research

28 pages, 12165 KiB

Open AccessReview

Recent Progress of Imprinted Polymer Photonic Waveguide Devices and Applications

by Xiu-You Han, Zhen-Lin Wu, Si-Cheng Yang, Fang-Fang Shen, Yu-Xin Liang, Ling-Hua Wang, Jin-Yan Wang, Jun Ren, Ling-Yun Jia, Hua Zhang, Shu-Hui Bo, Geert Morthier and Ming-Shan Zhao

Polymers 2018, 10(6), 603; https://doi.org/10.3390/polym10060603 - 31 May 2018

Cited by 38 | Viewed by 8148

Abstract

Polymers are promising materials for fabricating photonic integrated waveguide devices. Versatile functional devices can be manufactured using a simple process, with low cost and potential mass-manufacturing. This paper reviews the recent progress of polymer photonic integrated devices fabricated using the UV imprinting technique. [...] Read more.

Polymers are promising materials for fabricating photonic integrated waveguide devices. Versatile functional devices can be manufactured using a simple process, with low cost and potential mass-manufacturing. This paper reviews the recent progress of polymer photonic integrated devices fabricated using the UV imprinting technique. The passive polymer waveguide devices for wavelength filtering, power splitting, and light collecting, and the active polymer waveguide devices based on the thermal-optic tuning effect, are introduced. Then, the electro-optic (EO) modulators, by virtue of the high EO coefficient of polymers, are described. Finally, the photonic biosensors, which are based on low-cost and biocompatible polymer platforms, are presented. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Graphical abstract

27 pages, 1749 KiB

Open AccessReview

Green Strategies for Molecularly Imprinted Polymer Development

by Raquel Viveiros, Sílvia Rebocho and Teresa Casimiro

Polymers 2018, 10(3), 306; https://doi.org/10.3390/polym10030306 - 12 Mar 2018

Cited by 101 | Viewed by 8993

Abstract

Molecular imprinting is a powerful technology to create artificial receptors within polymeric matrices. Although it was reported for the first time by Polyakov, eighty-four years ago, it remains, nowadays, a very challenging research area. Molecularly imprinted polymers (MIPs) have been successfully used in [...] Read more.

Molecular imprinting is a powerful technology to create artificial receptors within polymeric matrices. Although it was reported for the first time by Polyakov, eighty-four years ago, it remains, nowadays, a very challenging research area. Molecularly imprinted polymers (MIPs) have been successfully used in several applications where selective binding is a requirement, such as immunoassays, affinity separation, sensors, and catalysis. Conventional methods used on MIP production still use large amounts of organic solvents which, allied with stricter legislation on the use and release of chemicals to the environment and the presence of impurities on final materials, will boost, in our opinion, the use of new cleaner synthetic strategies, in particular, with the application of the principles of green chemistry and engineering. Supercritical carbon dioxide, microwave, ionic liquids, and ultrasound technology are some of the green strategies which have already been applied in MIP production. These strategies can improve MIP properties, such as controlled morphology, homogeneity of the binding sites, and the absence of organic solvents. This review intends to give examples reported in literature on green approaches to MIP development, from nano- to micron-scale applications. Full article

(This article belongs to the Special Issue Molecularly Imprinted Polymers)

► Show Figures

Graphical abstract

Journal Menu

Journal Browser

Molecularly Imprinted Polymers

Share This Special Issue

Special Issue Editors

Special Issue Information

Keywords

Benefits of Publishing in a Special Issue

Published Papers (12 papers)

Research

Review

Further Information

Guidelines

MDPI Initiatives

Follow MDPI