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Light Responsive Polymer Membranes: A Review

Membranes 2012, 2(3), 440-477; doi:10.3390/membranes2030440

Review
Molecularly Imprinted Membranes
Francesco Trotta *, Miriam Biasizzo and Fabrizio Caldera
Department of Chemistry, University of Torino, Via Pietro Giuria 7, 10125 Torino, Italy; Email: miriam.biasizzo@unito.it (M.B.); fabriziocaldera@libero.it (F.C.)
*
Author to whom correspondence should be addressed; Email: francesco.trotta@unito.it; Tel.: +39-011-6707550; Fax: +39-6707855.
Received: 18 April 2012; in revised form: 20 June 2012 / Accepted: 26 June 2012 /
Published: 19 July 2012

Abstract

: Although the roots of molecularly imprinted polymers lie in the beginning of 1930s in the past century, they have had an exponential growth only 40–50 years later by the works of Wulff and especially by Mosbach. More recently, it was also proved that molecular imprinted membranes (i.e., polymer thin films) that show recognition properties at molecular level of the template molecule are used in their formation. Different procedures and potential application in separation processes and catalysis are reported. The influences of different parameters on the discrimination abilities are also discussed.
Keywords:
membranes; molecular recognition; polymers; template

1. Introduction

The growing attention dedicated to molecularly imprinted polymer (MIP) technology has led to the development of a wide range of applications in various fields, including filtration, chromatography and sensor sectors.

Although the term “molecular imprinting” was first used in 1931 [1], practical interest in the technique did not really take off until 1972, when organic polymers with predestined ligand selectivity were prepared by Wulff and Sarhan [2] and Klots and Takagishi [3].

Molecular imprinting technology is an approach to design molecular recognition sites on materials imitating natural recognition features, such as antibodies and receptors. The MIP’s range of applications is wide: they are used in drugs and biological derivatives separation and purification, chemical sensors, catalysis. MIPs are less expensive, stronger, resistant to elevated temperatures and pressures, and are mostly chemically inert compared with other biological systems [4].

The mechanism of the imprinting is simple to understand: a template molecule is entrapped in a polymer matrix during polymerization, so that the molecular information is traced in polymeric material in the cross-linked powders and the molecule shape, and its complementary chemical functionality persist in the matrix network after the complete extraction of the template from the matrix as cavities [5]. These cavities are the recognition sites for the same template molecule or similar: these molecules bind to the polymer matrix with a very high specificity [6].

There are two kinds of interaction between template molecule and functional monomers: a covalent interaction and a non-covalent interaction. The former type as reported by Wulff [2] creates bonds, such as ester, and is very stable; the latter type (first reported by Haupt [7]) gives electrostatic interactions and hydrogen bonds; it is weaker and a large amount of functional monomer is randomly grafted in the matrix. The non-covalent technique has been preferentially used for different reasons: in the first instance, non-covalent procedures are easily conducted, then removal of the template is carried out simply by continuous extraction, and in the end a great number of functionalities can be introduced into binding sites [8]. The non-covalent interactions could also be studied by quantum mechanical calculations, for example in the frame of density functional theory (DFT), investigating the binding energies between the template molecule and the polymer/copolymer, because many studies have shown that hydrogen bonding and short-range electrostatic interactions are responsible for macroscopic effects [9,10,11].

Membranes can show molecular recognition. For instance, pre-modification (surface functionalization) of PP microfiltration membranes and of PET track-etched membranes were obtained by immersing the membranes in an aqueous solution of PEG400 monomethacrylate and benzophenone. The pristine and pre-modified PP and PET membranes were functionalized with poly(MAA-co-EGDMA). The membranes thus prepared were placed between two filter papers and the vessel was filled with the polymerization mixture, then irradiated with UV light [12].

A comparison between two different methods of membrane preparation was proposed by Park et al. [13], who employed a “post implanting” and an “in situ implanting” procedure for the synthesis of imprinted membranes. From a morphological point of view, the membrane prepared by in situ implanting has a more compact structure than that prepared by post implanting: there are many microvoids in the post implanted membrane and the microparticle size is smaller than that of the membrane prepared using the in situ procedure. The adsorption selectivity of the D-Phe-imprinted membrane prepared by post implanting is higher than that of the one prepared by in situ implanting.

In most studies performed on MIP membranes, the recognition sites are distributed in the bulk polymer phase, so their accessibility is limited, giving low membrane performance. Many studies have been carried out with a view to overcoming this problem, including, for example, an approach to the production of MIP membranes with an ordered porous structure using the method proposed by Widowski and co-workers [14]: the highly ordered porosity is produced by evaporating a polymer solution (prepared in a volatile solvent) under controlled humidity. The development of this technique was proposed also by Lu et al. [15] to gain ordered porosity from random poly(styrene-co-acrylonitrile) using THF as a solvent using the water-assisted method in the presence of template. SEM analysis showed the highly ordered and regular pore structure of the MIP membrane surface and the cross-section. Permeation experimentation results showed that the MIP membranes recognized the template molecule effectively and transported it with good efficiency. This could be attributed to the porous structures of the MIP membranes, because the ordered porous structures on the surface and in the cross section allow the accessibility of recognition sites, thus the MIP membrane showed the highest transport rate toward the template molecule.

The work of Ma and co-workers [16] described a new kind of polymer employed for the preparation of molecularly imprinted membranes, rarely reported in literature: the chitosan (CS). CS is a non-toxic, biocompatible, biodegradable, and amino-polysaccharide obtained from one of the world’s most abundant biopolymers, chitin. Its special properties make CS widely used in drug delivery and environmental protection applications. It can be used for membrane separation by ion exchange, chelation and adsorption.

Nanotechnology offers a new perspective for the production and the application of MIPs: it is possible to prepare MIPs as nanomaterials (nanofibers, nanospheres, etc.), but it is also possible to graft nanostructured MIPs onto conventional surfaces, i.e., PVDF filters and glass fiber, to obtain a specific new material [17,18,19,20,21,22].

Thin inorganic or organic films with ion-sensitive field-effect transistors (ISFETs) and piezoelectric quartz crystals could be present in this type of material. According to Zayats et al. [23], a thin TiO2 film was obtained with sol-gel polymerization of a mixture of Ti(IV) butoxide and carboxylic acids (4-chloro-phenoxyacetic acid, 2,4-dichloro-phenoxyacetic acid, fumaric acid and maleic acid), thereby giving the imprinting. These films were assembled on the ISFET gate interface. An imprinted polymer membrane was then prepared by mixing AAm, 3-(acrylamido)phenylboronic acid, MBAA, N,N,N',N'-tetramethylethylenediamine and imprinted with nucleotides (AMP, GMP and CMP) to obtain the selective recognition.

A novel technique for the synthesis of MIMs imprinted membranes on glass-fiber membranes and Teflon filters was described by Ceolin et al. [24]. Polymer films were prepared on microporous glass-fiber membranes. Polymerization took place under an argon flow and using UV initiation. This study was carried out to optimize the synthesis procedure, template removal, rebinding tests and regeneration of the polymers. The optimum was found to be 1:4:20 (template:functional monomer:cross-linker), the conventionally described ratio in MIP-related literature [25,26,27].

MIPs are stiff materials that can be ground and powdered and are insoluble in all solvents. MIPs are not known as flexible films, however Sreenivasan [28] proposed a new approach to prepare and evaluate the corresponding properties of a molecularly-imprinted semi-interpenetrating polymer (semi-IPN) as a film. The monomers employed were 2-hydroxyethylmethacrylate and EGDMA and they were added to a solution of polyurethane (PU) in chloroform. The mechanical tests performed showed that MIP–IPN ultimate stress and strain is good, although less than that of PU.

The research aim to improve membrane flexibility continued with the work of Fan et al. [29], in which they performed, as a first step, synthesis of imprinted particles following a traditional procedure (employing MAA as functional monomer, glycol dimethacrylate as crosslinker). As a second step, the powdered MIP was added to a polysulfone (PSf) solution containing PEG 600 to improve flexibility and mechanical strength.

In addition to the polymerization onto filter plates in order to improve selectivity, it was suggested that nanofiber membranes could be synthesized by electrospray deposition (ESD) [18]. MIP membranes with a higher surface area can give two orders of magnitude higher flux and permselectivity compared with those prepared using conventional methods. ESD is a method used to obtain MIP membranes with a large surface area, consisting of polymeric nanofibers whose diameters range from nanometers to micrometers, by the action of an electric field imposed on a polymeric solution. With ESD, the morphology and the diameter of the electrosprayed membranes could be effectively controlled.

A novel molecularly-imprinted hybrid membrane [30] was prepared using sodium alginate (SA) as the polymer and 3-aminopropyltriethoxysilane (APTES) as a precursor for introducing an inorganic component into the organic matrix and as a cross-linking agent to improve the mechanical strength of the SA membrane. When APTES content was low (<30 wt % in comparison to SA amount), almost no selective ability was found, due to the loose and excessively flexible structure. When the APTES content was higher than 40%, the MIP had a poorer ability to form template-polymer interactions. The addition of APTES increased the compatibility between the organic and inorganic phase via covalent interactions.

In a new study by Zhang et al. [31], the selective recognition was evaluated with new protein MIM multi-walled carbon nanotubes (PMIM/MWNTs) were synthesized employing AAm as the functional monomer, MBAA as the cross-linker and bovine serum albumin (BSA), a protein concentration standard for many biochemical and immunological applications, as the template molecule. Comparing PMIM/MWNTs to the non-imprinted ones (nPMIM/MWNTs), the PMIM/MWNTs exhibited discriminatory recognition for BSA (2,6-fold increase in affinity) and selective ability adsorption capacities towards BSA than human serum albumin, pepsin, bovine blood hemoglobin and horseradish peroxidiase.

However, the first proposal of an easy technique for obtaining efficient MIMs with non-covalent bonds was made by Kobayashi and co-workers in 1995 [32] using the phase inversion technique to form membranes and subsequently used by the same research group [5] and by other authors [33,34,35,36,37,38]. The technique focuses on the casting of a copolymer solution of P(AA-co-AN) containing the template molecule on a glass plate, then making it coagulate in a non-solvent bath (i.e., water) and finally washing the membrane with an opportune solvent in order to remove the template molecule and expose the corresponding cavities. The coagulation bath assumes great importance because it is able to give the membrane the right permeability and optimum performance, so the temperature of this bath was extensively studied in order to obtain the best results [39].

As far as membrane technology is concerned, one of the most common polymeric membranes used for molecular recognition is PAN and its copolymers. Tasselli et al. [40] published a study on the binding capacity of a PAN membrane, varying the amount and the type of the functional monomers (IA, AA, AAm), using the phase inversion technique in a polar solvent.

Kobayashi et al. [41] in 2008 proposed a novel approach to the synthesis of molecularly-imprinted membranes employing supercritical carbon dioxide (ScCO2) as an antisolvent, thereby inducing the phase separation of the polymer solution. Membrane preparation employing ScCO2 is similar to conventional immersion precipitation of polymers, but achieves better results. Advantages: since the ScCO2 dries the polymer membrane rapidly, it does not collapse and at the end there are no traces of organic solvents that could be removed from gaseous CO2 after decreasing the pressure.

2. Advanced Polymeric Membranes: Synthesis and Applications

2.1. Pharmaceutical and Food Applications

Malaisamy et al. [38] studied MIP blend membranes made of cellulose acetate (CA) and sulfonated PSf with different compositions (100/0, 95/5, 90/10 and 85/15), employing the biomarker Rhodamine B (Rh B) as the template molecule and using the phase inversion method. They hypothesized that sulfonated PSf content influenced MIP surface hydrophobicity and eventually they observed that blend membranes with 95/5 composition had the highest binding capacity.

Trotta et al. [42] suggested using P(AA-co-AN) for the production of membranes with an asymmetric pore structure, prepared using the phase inversion technique. The membranes containing the antibiotic tetracycline hydrochloride (TCH) template were prepared using the same method, but adding the required amount of the template molecule (2 wt %). Chloramphenicol, TCH analog, was used to test the selectivity of the imprinted membrane. The resulting membrane shows molecular recognition properties for the highly water-soluble TCH. About 140 μg (0.29 μmol) of TCH were retained per gram of imprinted membrane. Chloramphenicol, that has similar solubility, was less recognized (no more than 0.16 μmol/gmembrane), as it is possible to observe in the following Figure 1.

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Figure 1. Uptaken amount of TCH and chloramphenicol in the MIM for TCH and NMIM: (■) tetracycline hydrochloride into P(AA-co-AN) NMIM; (●) TCH in the P(AA-co-AN) MIM; (▲) chloramphenicol in the P(AA-co-AN) MIM; ( Membranes 02 00440 i001) chloramphenicol in the NMIM.

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Figure 1. Uptaken amount of TCH and chloramphenicol in the MIM for TCH and NMIM: (■) tetracycline hydrochloride into P(AA-co-AN) NMIM; (●) TCH in the P(AA-co-AN) MIM; (▲) chloramphenicol in the P(AA-co-AN) MIM; ( Membranes 02 00440 i001) chloramphenicol in the NMIM.
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Fan et al. [29] employed the chemotherapeutic agent trimethoprim (TMP) as template molecule, for imprinting particles following a traditional procedure (MAA was the functional monomer and the glycol dimethacrylate as crosslinker), then the powdered MIP was added to a polysulfone (PSf) solution containing PEG 600 to improve flexibility. The mixture obtained was cast and it was seen that when the ratios of MIP, PSf and additive PEG were 30 wt %, 20 wt % and 10 wt %, respectively, the blend membrane had selective recognition to TMP in addition to flexibility and mechanical strength.

More generally, it is possible to recognize several biomolecules in solution selectively, as studied by Silvestri et al. [43]: MIMs of biotechnological interest were obtained either by the coagulation or modification of NMIMs introducing imprinted nanoparticles. They observed that membranes of P(AN-co-AA) imprinted with uric acid, a marker for several diseases, such as gout, showed good recognition capacity and selectivity towards the template (the detection of uric acid was 2.4 times higher than theophylline). In addition, porous supports of EVA-dextran blends were prepared using α-amylase as a template: the selectivity of this device was 1.96 times higher than that of albumin. In some cases, the recognition properties of MAA-co-AA membranes were improved by loading imprinted cross-linked MMA-MA nanospheres. In this way, different membranes were obtained for application in the biomedical field or for various biotechnological uses, on account of their biomimetic behavior. The same author [44] subsequently suggested preparing new polymeric systems through MIP for potential application in extracorporeal blood purification. Membranes based on EVA material, produced using the phase inversion method were prepared to remove low density lipoproteins and cholesterol (LDL) from plasma employing the model compounds phosphatidylcholine (PC) and α-amylase (αA) as target molecules. In both cases, the results were positive: the selectivity of the PC-MIM was tested passing through the membrane solutions containing phosphatidylserine (PS) and phosphatidylinositol (PI), and the PC-imprinted membrane exhibited a very higher adsorption of PC in comparison to PS and PI analogs. Regarding αA selectivity and the imprinting effect, they were confirmed in a similar test by the higher uptaking of αA in respect to albumin (ALB), as is shown in Table 1.

These membranes introduced specific cavities into the polymer to bind and selectively recognize PC and α-amylase. The devices thus realized could be useful for dialysis, blood filtration, and fractioning in the biomedical field.

Table Table 1. Percentage adsorption during rebinding, selectivity, and competitive selectivity tests in respect to initial solute in the test solution of (a) template PC and the analogs PS and PI, (b) template α and the analog ALB.

Click here to display table

Table 1. Percentage adsorption during rebinding, selectivity, and competitive selectivity tests in respect to initial solute in the test solution of (a) template PC and the analogs PS and PI, (b) template α and the analog ALB.
TABLE (a)% adsorbed in rebinding test% adsorbed in competitive rebinding test
MoleculePC-imprinted membraneControl membranePC-imprinted membraneControl membrane
PC (template)78.056.0968.224.11
PS0.150.295.910.96
PI0.100.16--
TABLE (b)% adsorbed in rebinding test% adsorbed in competitive rebinding test
MoleculeαA-imprinted membraneControl membraneαA-imprinted membraneControl membrane
αA(template)43.4612.2139.559.33
ALB8.306.126.716.89

Pegoraro et al. [45] focused their work on the possibility of adopting MIP based on polymeric membranes imprinted with PC for use in their research on regression of atherosclerosis. The polymer matrix was based on EVA with an ethylene molar content of 44% and three different amounts of PC template molecule (PC100 = 62.5 mg/gmembrane; PC200 = 117.5 mg/gmembrane), obtaining the membranes by phase inversion. Both membranes PC100 and PC200 possessed high binding capabilities (78.6% of the initial PC amount in the solution test); phospholipids similar to PI and phosphatidylethanolamine (PE) were used to test the selectivity of the membranes and both PC100 and PC200 showed selectivity for PC and not for PI and PE.

Sreenivasan [28] employed cholesterol, an important component in hormonal systems, as the template molecule, using as monomers 2-hydroxyethylmethacrylate and EGDMA, and adding a solution of polyurethane (PU) in order to obtain a semi-IPN device. Cholesterol absorption is greater in MIP–IPN (5.52 mg absorbed by 100 mg of polymer) than in control semi-IPN (0.72 mg absorbed by 100 mg of polymer) and PU (2.61 mg absorbed by 100 mg of polymer). Testosterone was chosen as a molecule with similar structure and shape to cholesterol, to evaluate MIP’s selectivity for cholesterol. These membranes imprinted with cholesterol have shown very low affinity for testosterone (0.57 mg absorbed by 100 mg of MIP–IPN; 0.62 mg absorbed by 100 mg of semi-IPN polymer; 1.87 mg absorbed by 100 mg of PU).

A MIM targeted to α-tocopherol (α-Toc) [46], a type of vitamin E, was prepared by phase inversion of polymer from a template-containing monomer, α-tocopherol methacrylate (α-TMA) and copolymerized with AN from a DMSO solution in a coagulation non-solvent water bath. The results were that the amounts of α-Toc joined to imprinted and non-imprinted membranes were 20.8 ± 0.4 and 2.2 ± 0.1 μmol/g, respectively: the imprinted membranes showed higher affinity and selectivity towards α-Toc than to the 4-chromanol analog. Evidence shows that separation was achieved with a separation factor of 15.5 for α-Toc/4-Chr using a simple filtration procedure with high flux permeation.

The same author presented an evolution of the above study [47]: α-TMA was used as a functional monomer and copolymerized with divinylbenzene to prepare microparticles and then granulated. In this way, several hybrid MIMs (HMIP) containing the polymer powders were obtained using polymer supports such as PSf, CA and Ny. All HMIP membranes prepared using the phase inversion technique showed selective binding of α-Toc over its derivative, δ-tocopherol, exhibiting efficiencies of 0.49 for MIP powder and 0.60, 0.64, and 0.53 for PSf, Ny and CA-HMIP, respectively. Again, the same research group proposed, in 2009 [48], an MIP obtained by phase inversion targeted to α-Toc developed by polymer membrane scaffold made of PSf containing calix[4]resorcarenes and showing non-covalent host-guest interactions with the template. The amount of α-Toc bound to the imprinted and non-imprinted membranes was 41.1 ± 0.9 and 22.2 ± 1.1 μmol/gmembrane, respectively. A separation factor of 14.5 was obtained for α-Toc relative to its analog, 2-napthol (2-Nap).

Donato et al. [49] suggested extracting folic acid, a constituent of the vitamin B group, from aqueous solutions, using a novel procedure based on the membrane separation process employing MIMs prepared using the phase inversion technique. The MIMs were made with poly(AN-co-Aamide) and folic acid as the template molecule. A reference sample was prepared with poly(AN). In particular, solvent evaporation made it possible to obtain poly(AN-co-Aamide) imprinted membranes, which showed a specific binding capacity of 5.3 μmol/gmembrane. Blank membranes without the template molecule showed a low specific binding coefficient of 1.0 μmol/gmembrane. PAN-based membranes, on the other hand, showed low folic acid retention of 1.5 μmol/gmembrane (if prepared in the presence of the template) and 0.9 μmol/gmembrane (if prepared in the absence of the template). The results are reported in Figure 2.

Ma et al. [50] studied the release of naproxen, a nonsteroidal anti-inflammatory drug, using variables such as polymer type and concentration, solvents and casting conditions, and observed that naproxen caused a reduction in Tg (glass transition temperature) of the amorphous poly(lactide-co-glycolide) and poly(D,L-lactide) compared to drug loads in dry casting conditions. Release profiles for all the polymers tested followed a two-stage model: initial diffusive release, followed by zero-order release due to polymer decay.

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Figure 2. (a) pH effect on the binding capability of blank and MIM P(AN-co-AA); (b) retention of folic acid by PAN and P(AN-co-AA) prepared by solvent evaporation.

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Figure 2. (a) pH effect on the binding capability of blank and MIM P(AN-co-AA); (b) retention of folic acid by PAN and P(AN-co-AA) prepared by solvent evaporation.
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Saljoughi et al. [51] synthesized asymmetric CA membranes for hemodialysis with the phase-inversion method, using PEG 400 as the additive and NMP as the solvent: increasing the PEG concentration and reducing the CA concentration resulted in increased insulin/HSA diffusion and improved the formation of macrovoids in the membrane sublayer. In addition, these conditions increased the thermal and chemical stability of the membranes.

MIMs templated with puerarin [52] were prepared by coagulation with P(AN-co-AA). The copolymer–DMSO solution with puerarin, a recently studied plant-derived molecule having several effects on human health, was obtained at various temperatures: increasing P(AN-co-AA)’s molecular weight and decreasing the coagulation temperature (25 °C) led to an improvement in puerarin recognition by the membrane and also in the purity of puerarin, which rose from 56.51 to 98.41 wt %.

Zhang et al. [53] used oleanolic acid (OA), a molecule that exhibits antitumor and antiviral properties, as the template molecule, polyamide-6 (PA6) as the membrane and PSMA to prepare PA6/PSMA-OA molecularly imprinted composite membranes by the phase inversion method in ScCO2. They tested different conditions to obtain the optimum, i.e., the mass ratio between PSMA and OA (from 3:1 to 8:1), the temperature of ScCO2 (from 35 to 50 °C) and the pressure of ScCO2 (12 MPa to 17 MPa), finding that the highest adsorption rate and purity of OA were 50.41% and 96.15% respectively.

One of the aims of MIP-related research is to increase selectivity and the extent of the gate effect (the morphology and diffusive permeability of the MIP membrane is affected by different issues that play a key role in the recognition properties of MIP membranes and it is very important to control them). These issues are polymer flexibility, density, the amount of specific binding sites and the swelling/shrinking capability in the presence of the print molecule. To optimize these factors, it could be possible to control the radical polymerization in MIP synthesis. Living radical polymerization is induced by “iniferter” (initiator-transfer agent-terminator), which acts as an initiator, retarder, terminator and other transfer reactions. The degree of polymerization and the primary structure of the synthesized polymer can be conventionally controlled by reaction time and the degree of branching by the time of ultraviolet (UV) irradiation [54]. Living polymerization was employed for the grafting of a polymer imprinted with the bronchodilator theophylline using photoactive iniferter immobilized on the cellulose dialysis membrane surface. The surface morphology of the MIP membrane varies with time of polymerization and UV irradiation.

An approach to the ESD technique was proposed by Yoshimatsu et al. [19] using PET as a support for imprinted nanoparticle encapsulation. The study was performed to detect traces of propanolol in an aqueous solution containing (R,S)-propranolol hydrochloride, (S)-propranolol hydrochloride and (R)-propranolol hydrochloride. The interesting characteristic of these nanofibers is that there is no loss of particles, so the same composite nanofiber could be reused more than 10 times after regeneration, without loss of this property. The imprinted composite nanofiber membrane tested can selectively extract propranolol from solution samples.

The flavone luteolin, with antioxidant effects, was used as the template molecule employed by Zhang et al. [55] for the preparation of composite membranes for grafting the upper side of the Al2O3 microporous asymmetric tubular membranes. APTES is the functional monomer and TEOS as the crosslinker. Rutin (RT) was used as the competitive recognized molecule, because its molecular structure is similar to luteolin, but there is a big difference between their permeability performances through the composite membrane: the test performed on a mixture showed that the estimated separation factor of luteolin and RT was 14,12.

Trotta et al. [56] studied the retention of the flavonoid naringin (4,5,7-trihydroxyflavanone-7-rhamnoglucoside) (NG), a molecule that like limonin, hesperidin and other molecules contributes to the bitter taste of orange juice, being present in the rind of citrus fruits. The co-polymer employed was P(AA-co-AN) with 16.6 mol% of AA and was synthesized with template molar content 2%–4%. The scheme of the preparation is shown in Figure 3. Molecular imprinted membranes, as expected, were able to bind NG effectively, whereas the non-imprinted membrane did not show any retention property for NG. The greater amount of NG entrapped in the P(AA-co-AN) membrane (4%), does not lead to an increase in the retained amount of the template, presumably because most of the NG binding sites are not correctly positioned or are inaccessible.

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Figure 3. Scheme of NG-MIM preparation.

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Figure 3. Scheme of NG-MIM preparation.
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Tasselli et al. [40] published a study on the binding capacity of different PAN copolymer membranes with NG. Four kinds of membrane were obtained using the phase inversion technique in a polar solvent: polyacrylonitrile (PAN), poly(acrylonitrile-co-itaconic acid) (P(AN-co-IA), poly(acrylonitrile-co-acrylic acid) (P(AN-co-AA) and poly(acrylonitrile-co-AAm) (P(AN-co-AAm) at two ratios: (3:1 and 6:1). All membranes presented good specific recognition properties, especially P(AN-co-Aamide), which showed the best overall (12.9 μmol/gmembrane) and specific (9.0 μmol/gmembrane) binding capacity.

NG was also the target molecule for a study by Ma et al. [16]: a MIM was prepared in aqueous media using CS as functional polymer, NG as template molecule, PEG as porogen and H2SO4 as crosslinking agent and the membrane was obtained by the phase-inversion technique. The MIM showed excellent performance with the mass ratio CS:NG = 15:1. The NG–CS MIM was used to separate NG from aqueous mixtures of NHD and NG and the highest permeation percentage was 11.16% for eight hours.

NG recognition was also achieved by Donato et al. [57] by using surface functionalization of PVDF microfiltration membranes, conjugating the imprinting and the membrane technology. They made use of 4-VP as the functional monomer and EGDMA as the crosslinker, with the help of benzoin ethyl ether (BEE) as the photoinitiator, using varied concentrations of the 4-VP and EGDMA to obtain membranes with different modification degrees. As it is possible to observe in the Figure 4(a), the highest specific binding was found in MIMs with modification degree value about 2100 μg/cm2 and after the selective recognition test performed with the structural analog RT, it has been possible to assert the stronger affinity of this new kind of MIMs for the template than the analog.

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Figure 4. (a) NG retention on poly(4-VP/PVDF) NR-imprinted and its corresponding blank membrane at different modification degree; (b) Binding properties of NG-imprinted membrane and its corresponding blank.

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Figure 4. (a) NG retention on poly(4-VP/PVDF) NR-imprinted and its corresponding blank membrane at different modification degree; (b) Binding properties of NG-imprinted membrane and its corresponding blank.
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To perform a permselective separation of lysozyme, a very important protein in human health, Chen et al. [58] presented a novel method to obtain a polymeric membrane based on a copolymer P(AN-co-DTCS) onto which AA and MBAA were crosslinked in the presence of lysozyme as the template molecule, by UV irradiation. The membranes so obtained were tested with a mixture of lysozyme and BHb or lysozyme and cytocrome c (Cyt c) and the results showed that MIMs have high selectivity performances towards lysozyme and not towards BHb and Cyt c, giving a selectivity factor of 2.51 for lysozyme vs. BHb and 2.13 for lysozyme vs. Cyt c, as it is possible to see in Figure 5.

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Figure 5. Selectivity activity of MIM and NMIM towards mixture containing lysozyme and BHb (a) and Cyt c (b).

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Figure 5. Selectivity activity of MIM and NMIM towards mixture containing lysozyme and BHb (a) and Cyt c (b).
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Particular attention has to be focused to the sensoristic applications of MIMs.

Propofol (2,6-diisopropylphenol) is an intravenous anesthetic with a short sleep-induction period. Metabolic rates vary from one individual to another, making continuous monitoring of propofol preferable. The most suitable monitoring system for an anesthetic would be an on-line biosensor using an antibody or a molecularly imprinted polymer (MIP)-based detection system. Petcu et al. [59] proposed the synthesis of a propofol-recognizing polymer to obtain a detection system for a sensor application for blood solutions: they employed EGDMA as crosslinker, 1,1'-azo-bis(cyclohexanecarbonitrile) as catalyst and 4-acetoxystytrene. They polymerized the membrane over polytetrafluoroethylene (PTFE), cellulose and nylon filter membranes and tested the selectivity in blood solutions spiked with known amounts of test-molecules. The results showed it to be a good method for the recognition of propofol and the test was bias-free.

MIMs were also used to concentrate and analyze propanolol, a beta-blocker drug, in urine and blood samples, and work concerning this application was reported by Renkecz et al. [60]. Oxprenolol was used as an analog to test membrane selectivity. The cross-linked polymer was prepared from MAA and EGDMA. Propranolol was detected from urine samples around the minimum required performance limit and from blood samples in the typical relevant concentrations. Specificity, selectivity and repeatability tests confirmed that this new method matched the requisites for biological sample analysis.

In the field of antibiotics, Rebelo et al. [61] published a study on MIMs for the TMP, in which they described the preparation of new TMP MIM-based ion-selective electrodes. The polymeric sensor was synthesized with methacrylic acid 2-VP functional monomers, including the template molecule. The sensing material was dispersed in a PVC matrix and plasticized with o-nitrophenyl octyl ether. All sensors with MIMs revealed a linear behavior against the logarithm concentration of TMP along a wide concentration range.

A new biomimetic sensor for enrofloxacin, was prepared by Kamel et al. [62], who described the development of enrofloxacin MIP-based ion-selective electrodes. The sensor is produced with methacrylic acid and/or 2-VP templated with enrofloxacin. The sensing materials thus built are dispersed in a PVC matrix plasticized with o-nitrophenyl octyl ether (oNPOE). The effect of pH on the potentiometric response was investigated in acetate or Tris buffers with a pH range of between 4 and 9. The sensitivity of the sensors was stable from pH 4 to 7 and dropped above pH 7. Both MAA and MAA-VP based sensors showed good potentiometric analytical properties, able to distinguish enrofloxacin from other fluoroquinolones in sample solutions.

With a similar synthesis procedure, Guerreiro et al. [63] produced new chlortetracycline ion-selective electrodes with the intention of enhancing selectivity with the improvement of analyte recognition through MIPs. The new sensor was synthesized with MAA and AA functional monomers and cross-linked by EGDMA containing the template molecule. The sensing materials were then distributed in a PVC matrix and plasticized with oNPOE. The sensors were used to analyze contaminated fish, synthetic urine and serum samples. The MAA-based MIPs had a greater affinity for the template than AA-based ones. Two different operational pH ranges could be indicated for these electrodes: 1.5 to 3 and 7 to 12 pH.

Almeida et al. [64] proposed the construction of sulfadiazine and sulfamethoxazole selective electrodes based on imprinted sol-gel (ISG) material. The ISG was employed as the electroactive material on PVC membranes selective for sulfadiazine and sulfamethoxazole, prepared by the inclusion of ISG particles into the PVC matrix. The sol-gel membranes were obtained by coating a graphite support with a small amount of the viscous ISG solution. The best performance was given by ISG particles in PVC, concluding that these sensors are appropriate for real sample applications. The proposed sensors for sulfadiazine and sulfamethoxazole operated suitably under laboratory conditions, with good precision of the analysis for both sulfonamides.

2.2. Polymer Membranes for Chiral Recognition of Amino Acids and Nucleic Acids

In 1997, Yoshikawa et al. [65] presented alternative molecularly-imprinted polymeric membranes prepared from a polystyrene resin bearing D-amino acids or L-amino acids. The membrane prepared from a DLDE derivative made of D-amino acids and imprinted by Boc-D-Trp recognizes the D-isomer in preference to the corresponding L-isomer. Steric effects, interaction between the carboxyl group in the print molecule and the amino group in the tetrapeptide residues are considered important factors and electrodialysis of the racemic amino acid solution shows that permselectivity directly reflects its adsorption selectivity. In a later work [66], protected amino acids Boc-L-Glu(OBzl), Boc-L-Gln, Boc-L-Lys(4-Cl-Z), and Boc-L-Leu/H2O were used as the imprinting molecules and the membrane materials were prepared using the Merrifield technique. The membrane imprinted with Boc-L-Trp or Ac-L-Trp, showed selectivity to the print molecule family. On the other hand, the membrane containing tetrapeptide residues of L-amino acids and imprinted by an L-amino acid derivative, recognized the L-isomer over the D-isomer.

A similar work was proposed on molecularly-imprinted polymeric membranes prepared from non-chiral synthetic polymer carboxylated PSf [67]. Z-D-Glu or Z-L-Glu was adopted as print molecules. Membranes imprinted by Z-D-Glu recognize the D-isomer over the corresponding L-isomer, and vice versa. The amino acid preferentially adsorbed by the membrane was also selectively permeated by electrodialysis.

A more recent development of the previously cited works [68] consists of a polystyrene resin containing tetrapeptide of Gly and using the D- or L-isomer of Boc-Trp as a print molecule. The membrane imprinted with the D-isomer recognized the Ac-D-Trp well and the one imprinted with the Boc-L-Trp had specific recognition for Ac-L-Trp. These two types of membrane exhibited optical resolution ability and there was adsorption selectivity in enantioselective electrodialysis.

Dzgoev et al. [69] successfully used MIP technology to obtain a membrane that showed enantioselectivity in order to distinguish between two enantiomers of N-carbobenzyloxy-L-tyrosine, employing for the synthesis of the membrane 1,1,1-tris(hydroxymethyl)propane trimethacrylate, MAA and AIBN. The same authors group prepared a Phe-imprinted membrane with two different methods: in situ implanting and post implanting, resulting in in situ D-Phe imprinted membranes thicker than the post implanting ones. The membranes prepared by the post implanting method therefore presented certain advantages: they selectively adsorbed D-Phe from a racemic solution, there are a great many macrovoids distributed in the matrix and the size of microparticles is smaller. In this way, the adsorption of D-Phe with post-implanting membranes is far higher than with in situ implanting membranes.

Reddy et al. [37] employed another kind of polymer (Ny6) to set up an L-Gln detection property both by heterogeneous batch and QCM electrode measurements. They carried out binding experiments in aqueous L-Gln, D-Gln, L-Glu and D-Glu solutions. The recognition experiments were extended to membrane filtration and quartz crystal microbalance response using the imprinted Ny6. In the batch binding experiments, the high recognition of L-Gln was confirmed by the imprinted polymer. The reduction of the frequency depends on the L-Gln concentration: the highest concentration of the L-Gln (20 μM) caused a big frequency change of the QCM. In contrast, the frequency reduction for the D-Gln solution was much lower in comparison to that detected in the L-Gln. Thus, the Nylon-6 MIM imprinted with L-Gln bound the L-Gln molecules with high affinity, as it is possible to observe in Figure 6.

Another polymeric support was employed by Wang et al. [39]: a modified sol-gel process, using CS and glycidoxypropyltrimethoxysilane (GPTMS), led to a dense and uniform enantioselective hybrid membrane (CS/GPTMS) with a low degree of swelling. It was imprinted with L-Phe and efficiently applied in chiral resolution of a D,L-Phe racemic mixture. The imprinted cavities gave considerable improvement in chiral resolution, reinforcing the binding ability and delaying their diffusion.

Ny6, Ny6,6 and terephthalic phenylene [70] polyamide (TPPP) were functionalized by phase inversion molecular imprinting to add L-Phe binding sites. Formic acid was used as the solvent and the solutions had 20 wt % nylon and 8 wt % L-Phe. The resulting porous membranes behaved as membrane adsorbents that separated the L/D mixture of the substrate. The imprinted Ny6 and Ny6,6 presented high selectivity to the L-form substrate with respect to the TPPP membranes, but the imprinted TPPP membranes showed higher binding capacity with 0.57 μmol/g for L-Phe. The partition coefficients of L- and D-forms by the imprinted membranes were 6.8 for Ny6, 4.2 for Ny6,6 and 1.7 for TPPP. The imprinted Ny6, Ny6,6 and TPPP membranes had separation factors of L- and D-Phe of 1.1, 1.1 and 1.2, respectively.

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Figure 6. Frequency change of the L-Gln imprinted polymer-QCM sensor for L-Gln and D-Gln.

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Figure 6. Frequency change of the L-Gln imprinted polymer-QCM sensor for L-Gln and D-Gln.
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In order to successfully separate another aminoacidic racemic mixture (D,L-Ser), Son et al. [71] prepared an MIP composite membrane (MIPCM) with PSf as the polymeric support and D-Ser as the target molecule. The preparation was carried out by interfacial polymerization and the MIPCM obtained gave a good optical resolution of D- and L-Ser (Figure 7). The efficiency of the separation depended on the operating pressure, for the reason that the intensifying operating pressure does not always lead to positive results: by increasing operating pressure from 2 to 3 bar, the amount of D- and L-Ser that passed through the membrane improved, but the composition of the D- and L-Ser in permeates became different, because the L-Ser seemed to compete with D-Ser to pass through the chiral space, diminishing the quantity of D-Ser in permeates and increasing that of L-Ser. Consequently, employing operating pressure under 2 bar, the authors observed that the best results were realized at 1 bar.

For the resolution of the water-soluble amino acid D,L-Phe racemic mixture molecule, Ul-Haq et al. [72] proposed and successfully developed enantioselective D- and L-Phe-imprinted AA/AN membranes. Recognition cavities were effectively formed in the prepared membranes, which had a nanoporous structure. The D- and L-Phe-imprinted membranes achieved rejection selectivities of 0.13 and 0.28, adsorption selectivities of 2.25 and 2.40 and permselectivities of 1.94 and 2.08 respectively.

In 2010 [73], the same author proposed another enantioselective D-Phe imprinted P(AA-co-AN) membrane prepared by phase inversion precipitation. The membrane selectively adsorbed template enantiomer over the other enantiomer and adsorption selectivity was higher at low solute concentrations and had a rejection selectivity of 0.82–0.64 and 0.91–0.63 for the filtration of 100 and 10 ppm racemic solutions. The membranes used were nanoporous without macrovoids and enabled the optical resolution of Phe.

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Figure 7. Separation of the D- and L-serine by the MIPCM from Ser racemate as a function of operating time as the operating pressure was varied from 0.5 to 2 bars.

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Figure 7. Separation of the D- and L-serine by the MIPCM from Ser racemate as a function of operating time as the operating pressure was varied from 0.5 to 2 bars.
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The reaction of lithiated PSf with the chiral terpenoid myrtenal led to a polymeric material having a chiral performance [74]. Molecularly-imprinted membranes were prepared with the myrtenal-PSf in the presence of print molecules (D,L-Glu). The control non-imprinted membrane also showed permselectivity for racemic Glu mixtures, but as with the other works, they found that the Z-D-Glu imprinted membrane showed D-isomer adsorption and diffusivity selectivity, and the same behavior was observed for the L-isomer.

Using a similar procedure, Hatanaka’s research group [75] synthesized novel polyureas with a chiral attribute prepared from L-lysine ethyl ester and 1,4-phenylene diisocyanate and investigated their optical resolution ability. They adopted N-α-protected Glu (Z-D-Glu or Z-L-Glu) as print molecules. Contrary to expectations, the polyurea control membrane showed adsorption selectivity. The D-isomer of Z-Glu imprinted membrane adsorbed, as expected, the D-isomer of Glu instead of the corresponding L-isomer and similar behavior was observed for the L-isomer. However, the Z-L-Glu imprinted membrane showed permselectivity for D-Glu, although L-Glu was incorporated into it: this inconsistency between adsorption selectivity and permselectivity was explained by the delayed transportation through the membrane of the enantiomer included in the membrane. Those MIMs showed chiral separation ability if a concentration gradient was adopted or potential difference was applied as a driving force for membrane transport.

Selective adsorption of Z-D-Glu was also proposed by Sueyoshi et al., employing as polymeric support nanofibers produced by ESD prepared from CA and Z-D-Glu as the print molecule. In addition to the proven permselectivity (D-Glu was transported through the Z-D-Glu molecularly imprinted nanofiber membrane in preference to the corresponding L-Glu and vice versa), these nanofiber molecule allowed an enhancement of the flux employed to pass the test solution through the membrane about two orders of magnitude higher than the usual MIM [76]. The same authors have recently presented an evolution of the previous work [77], employing PSf aldehyde derivatized nanofiber membranes: the target molecules were the same and a study on the influence of the flux through the membrane was performed, leading to the conclusion that the nanofiber aldehydic PSf also allowed an enhanced flux about two orders of magnitude higher than the usual MIM tests.

Yoshikawa et al. [18] made use of MIP electrosprayed nanofiber membranes prepared from carboxylated PSf and employing Z-D-Glu or Z-L-Glu as a template molecule. The results of the study reported that Z-D-Glu MIP nanofiber membranes have a preferential recognition for the D-isomer than the corresponding L-isomer, whereas Z-L-Glu MIP has high recognition for L-isomers.

MIM technology is also very useful for studying nucleotides. Yoshikawa et al. [78] used 9-ethyladenine as a print molecule and investigated the recognition and selective transport of adenosine and guanosine mixtures. The printed polymers were polystyrene resin (DIDE-resin), cellulose acetate and polysulfone. The MIMs synthesized in this way recognized/adsorbed adenosine instead to guanosine. However, guanosine was preferably permeated over adenosine, probably because of the relatively high affinity between adenosine and membrane.

According to Zayats et al. [23], a thin TiO2 film was obtained with sol-gel polymerization of a mixture of Ti(IV) butoxide and carboxylic acids (4-chloro-phenoxyacetic acid, 2,4-dichloro-phenoxyacetic acid, fumaric acid and maleic acid), thereby giving the imprinting. These films were assembled on the ISFET gate interface. An imprinted polymer membrane was then prepared by mixing AAm, 3-(acrylamido)phenylboronic acid, MBAA, N,N,N',N'-tetramethylethylenediamine and imprinted with nucleotides AMP, GMP and CMP. Selective detection by the imprinted sites was observed, which can be attributed to the complementary H-bonds between the nucleotide and the AAm units: in the case of AMP-imprinted AAm-acrylamidephenylboronic acid copolymer increased the gate-source potential change varying concentrations of AMP; in the presence of GMP and CMP the device had a low response. In the same way, the membrane imprinted with GMP and with CMP showed the same behavior in the presence of GMP and CMP respectively.

Sallacan et al. [79] created an AAm-acrylamidephenylboronic acid copolymer membrane with molecular recognition sites for the nucleotides AMP, GMP, CMP, and UMP, and also specific recognition sites for β-D(+)-glucose, D(+)-galactose, and β-D(−)-fructose. The membranes were built on piezoelectric Au quartz crystals or Au electrodes via electropolymerization or on the gate surface of an ISFET device by radical polymerization. The speed of the swelling process was slow, so the response times of the microgravimetric measurements were proportional to the swelling process, whereas the response time of the ISFET device was faster, but the microgravimetric and electrochemical analyses are one hundred times less sensitive than the ISFET devices.

Uracil, a molecule often employed for drug delivery, was selected by Wang et al. [39] as a template for preparing molecularly-imprinted membranes of poly(AN-co-MAA). This could be one application for bio-mimetic artificial components for studying RNA in biological organisms. Permeation experiments employing uracil or dimethyluracil showed that the imprinted membranes effectively recognized the template molecule.

Also Kobayashi et al. [41] used uracil as template molecule and prepared microporous PSMA membranes using ScCO2 as a nonsolvent for the phase inversion technology. Compared with water, the membrane prepared in ScCO2 showed regular cellular structure and no finger-like morphology. It also depends on the solvent used. They have studied the effect of DMF, DMSO and NMP, and the NMP gave a slightly isolated large pore size, whereas with DMF and DMSO the pore size was not isolated, rather it was interconnected. Uracil binding to the imprinted membrane prepared in ScCO2 was higher than that prepared in water: this occurs because most of the uracil dissolves in water during polymer coagulation. The results indicated that the URA-imprinted membrane prepared at 50 °C recognized and selectively bound URA than was the case at 35 °C. The resulting MIMs prepared at 35 °C and 50 °C bound URA with 9.2 ± 0.10 and 12.6 ± 0.06 μmol/g, respectively. Competitive binding studies were carried out with a solution containing URA/DMURA, URA/Thymine, and URA/Cytosine. The URA-imprinted membrane showed a high separation factor (α) of 17 for both URA/1,3-dimethylURA and URA/Thymine, and for URA/Cytosine, α = 13.

In their work, Pogorelova et al. [80] reported a new method for obtaining ISFET devices imprinted with specific recognition sites for NAD+, NADP+, NADH, and NADPH with a cross-linked AAm-acrylamidophenylboronic acid copolymer associated with the Al2O3 gate surface. The results demonstrated the successful imprint of the specific recognition sites for the oxidized cofactor NAD+ or NADP+ or the reduced cofactor NADH or NADPH and the assembly of functional sensing devices for the substrates. The observed selectivity existing for the oxidized pairs NAD+ and NADP+ or the reduced cofactors NADH and NADPH is remarkable: selectivity was induced by the additional single H-bonds given by the phosphate group present on the ribose unit of NADP+/NADPH.

2.3. Metal Ions

Due to the biological and environmental impact of metal ions, the development of new methods for selective separation, purification and determination of these compounds is of continuing interest.

Li et al. [81] reported the technology of using a Cu2+ template for nitrocellulose membrane-poly (vinyl alcohol)-ionic imprinting (NCM-PVA-I-I). In a condition of common cation and anion coexistence, NCM-PVA-I-I can distinguish copper with high selectivity, because the cavity in NCM-PVA-I-I is complementary to Cu2+. The Cu2+ entered the cavity and then formed an ionic association with the fluorescein anion outside the cavity by electrostatic effect.

Zhuqing et al. [20] reported a procedure for imprinting functional groups on sol-gel silica nanotubes for copper ion separation, using N-[3-(trimethoxysilyl)propyl]ethylenediamine (AAPTS) and CuSO4·5H2O to give Cu[AAPTS]22+ complex, and TEOS was added to form silica nanotubes. The best pH range for the extraction of Cu(II) was from 5 to 7.5, thereby avoiding the precipitation of the metal hydroxide and the protonation of the amine as the chelating groups. Adsorption and ion-recognition studies were carried out with Cu(II) and Zn(II) ions, and it was observed that the Cu(II) ion-imprinted silica nanotube membranes had a high adsorption capacity for Cu(II).

A QCM is an extremely sensitive surface sensor capable of measuring a nanogram level change in mass on the surface. QCM applications in biochemistry, environmental, food, and clinical analysis are very attractive, since this technique provides a label-less method for the direct study of biospecific interaction processes (e.g., the affinity interaction between antigen/antibody). Cai et al. [21] presented a study about the adsorption of metallothionein (MT) with the nanocrystalline TiO2 membrane on an electrode covered with a protein layer using a QCM. The crystals obtained were treated with MT solutions. It can be observed that adsorption of NIM to MT changes little for pH ranging from 7.1 to 10.3, whereas the change is obvious for NIM to MT. Actually, the washing of MIM leaves free cavities in the structure that are able to bind MT molecules better than NIM and selectively with respect to molecules of a similar structure.

A new approach was proposed for preparing a metal ion-imprinted polymer membrane through in situ polymerization using the Zn(II)-(2,2'-bipyridyl) complex as the template, 4-vinylpyridine (4-VP) as the monomer and PVDF membranes as the supporting material [82]. The imprinted membranes revealed higher selective adsorption and permeation for the template than the control non-imprinted membranes. Selective permeation of Zn(II) over Cu(II) was observed: the species with the fastest permeation was Zn(II)-o-diaminobenzene. The second fastest permeation was for Zn(II)-2,2'-bipyridil, followed by Cu(II)-2,2'-bipyridyl. Zn(II)-2,2'-bipyridyl and Cu(II)-2,2'-bipyridyl had a similar size, however, the simple small difference between Cu and Zn made the imprinted membrane selective for Zn(II) because of the size of cavities formed on the supporting membrane.

Another study on the permeability of 2,2'-dipyridyl as a solution to molecular recognition in a strong polar solvent was proposed by Wang et al. [83], employing porous PVDF a hollow fiber ultrafiltration membrane as a flexible and mechanically stable support. This study focused on the behavior of Ni2+, which plays a key role in the recognition process, and the binding target was [Nidipy]2+ complex. Various factors affect membrane permeation performance, such as ion concentration, cations and counterions and pH. Changes in pH make it possible to adjust the permeation performance of MIMs, making them suitable for use in controlled drug release applications.

As mentioned in paragraph 1, composite membranes are very interesting for various purposes. One of the most important aims is the recognition/adsorption/selective removal of metal ions. Sodium alginate (SA) was employed in combination with polyvinyl alcohol (PVA) and PEG to obtain a porous composite membrane imprinted with Cr(NO3)3·9H2O for the selective adsorption of Cr(III) ions (Cr(III)-PVA/SA) [84]. The effects of different parameters were evaluated in order to reach the best condition for the employment of the composite membrane: the concentration of template Cr(III) ions was found to be best at 0.078 wt %, the pH value of the solution had to be about 6.0 and temperature increases had a proportional effect on adsorption. The adsorption ability of Cr(III)-PVA/SA for Cr(III) ions peaks at 59.9 mg/gmembrane. Competitive adsorption studies were performed for the Cr(III)/Cd(II), Cr(III)/Cu(II) binary mixed system and the Cr(III)/Cd(II)/Cu(II) ternary mixed system: the MIP Cr(III)-PVA/SA is highly selective to Cr(III) ions due to the imprinted cavities in the adsorbent. The adsorption–desorption experiment shows that the Cr(III)-PVA/SA has an efficient reusability.

Vatanpour et al. [85] synthesized imprinted and non-imprinted membranes using Ni(II) ions and diphenylthiocarbazone ligand, employing MAA, EGDMA and AIBN. The study was carried out at different pH values: at pH 5, the extraction of Ni ion was around 32%; Ni ion adsorption increased with an increase in the pH of the solution from 7 to about 8. Above a pH of 8, the sorption of Ni ions decreased. To test the selectivity of Ni(II) versus Co(II) ions, pH 7 was employed and the selective permeation of Ni2+ versus Co2+ was observed. After several cycles of adsorption/desorption, the adsorption capacity was preserved at around 90% of the pristine membrane.

Cross-linked CS presented lower adsorption capability because of functional groups (-NH2) being cross-linked. Ion imprinting for the cross-linked CS adsorbent proposed by Shawky et al. [86] overcame this problem. The aforesaid authors used Ag+ as the imprinted metal ion in membrane synthesis. Competitive removals of Ag+/Cu2+ and Ag+/Ni2+ from mixtures were also studied: the non-imprinted membranes are selective for Cu2+ and Ni2+. CS Imprinted membranes showed relative selectivity coefficients for Ag+/Cu2+ and Ag+/Ni2+ 9 and 10.7 times higher than the non-imprinted membrane, respectively. In this way, the imprinted membranes are good for selective silver removal in a solution containing interferent ions such as Cu(II) and Ni(II).

Another study involving CS was proposed by Wang et al. [87], however, in this work, CS was used blended with PVA, in order to obtain a film-forming material, the metal ion-imprinted membrane (IIM) was prepared using silver ions as templates (Ag(I)-IIM). The adsorption capacity of Ag(I)- IIM for Ag(I) is stronger than other ions. Compared with Ag(I)-IIM, non-ion-imprinted membranes (NIIM) for all ions are similar and have a poor adsorption capacity.

2.4. Herbicides, Pesticides, Organic Pollutants

Zhu et al. [88] prepared a novel thin layer composite MIP membrane selective for monocrotophos (MCP) pesticide by means of in situ polymerization of MAA with EGDMA as crosslinker in Nylon-6, introducing specific binding sites into the membrane whilst maintaining its pore structure. Membrane selectivity was evaluated in filtration experiments also using three other organophosphorus pesticides (mevinphos, phosphamidon and omethoate): the composite MIP membrane had low binding affinity for the other pesticides in comparison to the good sorption of the template MCP membrane.

More recently, Donato et al. [89] employed poly-AN and its copolymers with MAA and AAm by a phase inversion technique, using dimethoate as template molecule and testing these membranes against dimethoate and its analog trichlorphon. The membrane obtained with the copolymer P(AN-co-MAA) obtained the best result for binding capacity and selectivity.

Kochkodan et al. [90] presented a set of composite membranes imprinted with desmetryn and ibuprofen made with PVDF, both hydrophobic (PVDF_phob) and hydrophilized (PVDF_phil), PSf, polycarbonate and nylon microfiltration membranes as supports for the specifically imprinted materials. 2-acrylamido-2-methyl-1-propane sulfonic acid and MBAA were employed for the preparation of desmetryn-imprinted composite membranes. Dimethylaminoethyl methacrylate and trimethylopropane trimethacrylate were used for the ibuprofen-imprinted membranes. It was observed that the imprinted membranes obtained showed selective binding of structurally similar toxic compounds and selective artificial recognizing elements with high affinity to the template molecules in aqueous solutions.

Prasad et al. [91] studied the specific retention of several pesticides: phorate, parathion, atrazine, dichlorovos, ethion, disulfoton, diazinon, 2,4-D, 2,4,5-Twere. For the polymer structure, they employed MAA, EGDMA, di-n-octylphthalate, 2-nitrophenyloctyl ether, bis(2-ethylhexyl) sebacate, tris(2-ethylhexyl) phosphate and high molecular mass poly(vinyl chloride).

Having thoroughly studied the effects of pH value, they concluded that the selectivity of the polymer inclusion membranes is remarkable compared to the corresponding non-imprinted ones used in potentiometric sensors. Moreover, the stability, reusability, portability and absence of memory effect mean that the novel phorate sensor device can be readily used in field monitoring.

Vishnuvardhan et al. [92] employed a degradation product of Soman, the pinacolyl methylphosphonate, as a template for imprinted polymer materials to create potentiometric sensors. They studied the comparison between three different MIP synthesis methods (bulk, suspension and precipitation) and the selectivity and the sensitivity of the different sensors was bulk > suspension > precipitation.

Pogorelova et al. [93] employed molecular recognition sites imprinted in hydrogel films associated with Au–quartz piezoelectric crystals. When the molecule met the recognition site, the hydrogel hydrated and swelled, which could be sensed by microgravimetric quartz crystal microbalance measurements. The imprinted polymer membrane ISFET devices were set up with AAm, sodium methacrylate and MBAA. The triazine herbicides used were atranex (atrazine), prozinex, tyllanex, simanex, ametrex, prometrex, and terbutex.

The imprinted films were immobilized on the gate surface of the ISFETs: the binding of the substrate to the selective site allows electronic transduction. The imprinted films were immobilized on Au–quartz piezoelectric crystals and the binding of the target molecule to the respective imprinted sites caused the polymer film to swell, thereby enabling the microgravimetric analysis of the different herbicides. The complementary electrostatic interactions and H-bonds between the polymerizable monomers and the substrate leads to a successful device for the specific recognition of different triazines.

Haloacetic acids (HAAs) are regulated by the US environmental protection agency (EPA) because of their risks to human health. These acids are monochloroacetic acid (MCAA), monobromoacetic acid (MBAA), dibromoacetic acid (DBAA), dichloroacetic acid (DCAA) and trichloroacetic acid (TCAA). Suedee et al. [94] developed sensitive conductimetric sensors for the detection of haloacetic acids (HAAs) in drinking water. They prepared MIPs with 4-vinylpyridine, ethylene glycol dimethacrylate. MIPs were immobilized on the sensor in a PVC membrane (MIP/PVC ratio of 1:2). The recognition selectivity of MIPs for HAAs was TCAA > DCAA > MCAA > DBAA > MBAA > TBAA.

Xie et al. [22] created an electrochemical device for the detection of the organophosphate pesticide chlorpyrifos (CPF), based on a molecular imprinted polymer on gold nanoparticles placed on a glassy carbon electrode (AuNP-gc electrode). CPF molecules assembled on the p-aminothiophenol (ATP) modified AuNP-gc electrode surface were fixed into the imprinted polyaminothiophenol (PATP) membranes and formed superficial imprinted sites. The imprinted PATP-AuNP-gc sensor is about 3.2-fold more sensitive than that of the imprinted PATP-Au sensor, and the sensitivity of the imprinted PATP-AuNP-gc sensor is about two orders of magnitude lower than that of the imprinted PATP-Au sensor.

In another work, Xie et al. [95] presented a study on 2,4-dichlorophenoxy acetic acid (2,4-D), imprinted in polypyrrole polymers (PPy) onto a carbon glass electrode. By performing cyclic voltammetry, it was possible to establish that the device made thus can conspicuously improve the sensitivity and selectivity of 2,4-D analysis, as well as potentially having good repeatability.

The same template molecule 2,4-D was used by Ayela et al. [96], to make a combination of silicon microcantilever arrays and MIPs, coupling a resonant electrochemical system (MEMS) to a responsive template layer prepared from 4-VP and trimethylacrylate. The resonance frequency decreased in presence of 2,4-D and subsequently increased when the 2,4-D is not present. The frequency shift depended on the volume of MIP deposited on the micromembrane: increasing the quantity of MIP, the frequency also increased, but tended to plateau values, as is shown in Figure 8a. The selectivity tests were performed with phenoxyacetic acid (POAc) at different concentrations: the array detected only the 2,4-D presence and not the analog POAc (Figure 8b).

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Figure 8. (a) Influence of the reduced volume of MIP on the resonance frequency of the array after rebinding of 2,4-D; (b) Detection of the rebinding of 2,4-D and POAc at increasing concentrations on a 2,4-D MIP and a NMIP.

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Figure 8. (a) Influence of the reduced volume of MIP on the resonance frequency of the array after rebinding of 2,4-D; (b) Detection of the rebinding of 2,4-D and POAc at increasing concentrations on a 2,4-D MIP and a NMIP.
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The success of photochemical initiation on the synthesis of imprinted membranes has been confirmed in literature. In the study published by Kochkodan et al. [97], PVDF microfiltration membranes were used, both unmodified hydrophobic (PVDF_phob) and hydrophilized (PVDF_phil). The PVDF_phil membrane was previously coated with a thin cross-linked polyacrylate layer over the whole surface of the membrane. The template molecule was the 1,3,5-triazine herbicide desmetryn and it was placed in radical-initiated cross-linking copolymerization with 2-acrylamido-2-methyl-1-propane sulfonic acid (AMPS) as the functional monomer and MBAA as the cross-linker in methanol. The reactions were carried out in two different ways: in variant A the mixture contained the photoinitiator BEE at a concentration of 2.5 mM and UV irradiated after 10 min of soaking; in variant B, the membranes were used coated by soaking in 100 mM solution of BEE in acetone for 5 min and subsequent drying at 40 °C for 15 min. The imprinting effect obtained was significant for thin layers of functional cross-linked copolymers on the surface of PVDF membranes using a coating of a α-scission type photoinitiator. As regards wettability by water, no change was observed for the functionalized PVDF_phil membranes, however the wettability of the PVDF_phob membranes increased with the hydrophilicity of the poly(AMPS-co-MBAA) layer.

A development of the semi-IPN technique was presented by Sergeyeva et al. [98]. In this work the authors prepared a thin and flexible film by adding oligourethaneacrylate to the monomer mixture (MAA/IA/AAm as functional monomers and tri(ethyleneglycol)-dimethacrylate as a crosslinker) for the MIP preparation, maintaining the highly cross-linked polymer feature. The template molecule used was atrazine. The MIP membranes were prepared on the basis of accurate computational modeling. The authors performed the study to verify herbicide recognition properties for the optimization of the composition of atrazine MIP with computational modeling. They identified methacrylic acid to be an optimal functional monomer for atrazine. The computational in-situ-polymerized MIP membranes obtained showed high adsorption for template molecules (12.5 mg/gmembrane) and high selectivity also for atrazine analogs.

Primary amines and some aromatic amines have are considered potentially carcinogens. Del Blanco et al. [99] have recently presented a study for the removal of these molecules (in particular 4,4'-methylenedianiline, (MDA)) from organic solvents as impurities or unreacted. They used different AN copolymers such as P(AN-co-IA), P(AN-co-AA) and P(AN-co-MAA), and obtained membranes by phase inversion technique. Binding experiments showed that template membranes are selective for the template molecule (binding capacity: 4.7 μmol/gmembrane) and distinguished between the template and its analog 4,4'-ethylenedianiline, EDA (binding capacity: 2.9 μmol/gmembrane). Aniline was also used to test the selectivity of both MIMs and NMIMs and it was seen entirely permeated through blank and imprinted membranes (Figure 9).

Membranes 02 00440 g009 1024
Figure 9. 4,4'-methylenedianiline, (MDA) retention and specific binding capacities of the membranes prepared using PAN and the different acrylic copolymers.

Click here to enlarge figure

Figure 9. 4,4'-methylenedianiline, (MDA) retention and specific binding capacities of the membranes prepared using PAN and the different acrylic copolymers.
Membranes 02 00440 g009 1024

Bryjak et al. [100] reported the preparation and properties of MIMs for the removal of suspect endocrine disruptor bisphenol A by using PSf with different degree of sulfonation (PSU) to prepare MIM by phase inversion technique, templated with bisphenol A. The results have shown that a high content of sulfonic groups (degree of sulfonation = 0.26 mol/mer), made the membranes less permeable to bisphenol A, as it is possible to see in the Figure 10.

Catalytic activity is usually proposed with milled MIPs and not membranes, on account of the powder’s larger surface activity. However, in other cases it is possible to obtain catalytic activity with membranes. Kalim et al. [101] proposed two different formats of MIMs to be used for a dehydrofluorination catalysis. The first one was a cellulose filter membrane coated with a polymer generated by MAA, EGDMA and AIBN imprinted with an analog of the chosen reaction (N-benzyl-isopropylamine). The second one was prepared by incorporating milled bulk polymers into PVA matrices mixed with glutardialdehyde on a cellulose membrane. Both types of membrane were tested for the catalytic effect on the dehydrofluorination of 4-fluoro-4-(p-nitrophenyl)-2-butanone. The coated membranes had no evident catalytic effect, whereas the PVA membranes containing the imprinted polymer particles did show catalytic effects, but these were obtained by allowing the substrate-product mixture to recirculate through the catalytic membrane, because the substrate did not have enough time to interact with the catalyst.

Membranes 02 00440 g010 1024
Figure 10. Permeability of PSf membranes with respect to bisphenol A. PSU has degree of sulfonation = 0.00 mol/mer; PSU1 has degree of sulfonation = 0.06 mol/mer; PSU2 has degree of sulfonation = 0.26 mol/mer; 5% is the amount of template (5 wt %).

Click here to enlarge figure

Figure 10. Permeability of PSf membranes with respect to bisphenol A. PSU has degree of sulfonation = 0.00 mol/mer; PSU1 has degree of sulfonation = 0.06 mol/mer; PSU2 has degree of sulfonation = 0.26 mol/mer; 5% is the amount of template (5 wt %).
Membranes 02 00440 g010 1024

Sergeyeva et al. [102] developed a portable biomimetic sensor device for the specific control of phenol content in water. The synthetic structure reproduced the active site of the enzyme tyrosinase in molecularly-imprinted polymer membranes. Those membranes with a catalytic activity were obtained by co-polymerizing the Cu(II)–catechol–urocanic acid ethyl ester complex with (tri)ethyleneglycoldimethacrylate, adding the elastic component oligourethaneacrylate: this procedure led to the creation of a thin, flexible, and mechanically stable highly cross-linked polymer membrane with catalytic activity. Investigation of the pH-influence demonstrated that pH-dependence peaked at neutral pH values: the oxidation of the catechol is inhibited at pH ≤ 5. In order to examine the selectivity of the new sensor system, catechol analogs (phenol, 4-nitrophenol, 1,2,3-trihydroxybenzol, 2-methoxyphenol, m-diphenol, p-diphenol, bisphenol A, 1,2-naphthalenediol, and 1,4-naphthalenediol) were added to the electrochemical cell. Unlike conventional biosensor devices made with mushroom tyrosinase that recognize different phenolic compounds, the sensor system developed had high selectivity: it gave catalytic oxidation of o-diphenols and no response was observed with their structural analogs (phenol, 4-nitrophenol, and 2-methoxyphenol, m-diphenol, p-diphenol, bisphenol A, 1,2- naphthalenediol, and 1,4-naphthalenediol).

3. Summary

In order to simplify the comprehension of this work, a summarizing table is proposed, with of template molecules, functional monomers, first authors and year of publication (Table 2).

Table Table 2. A summary of MIMs and templates.

Click here to display table

Table 2. A summary of MIMs and templates.
TemplateAuthorYearMonomer, Polymer Matrix And SupportRef.
Pharmaceutical And Food
α-amylaseSilvestri et al.2006poly(ethylene-co-vinyl alcohol), dextran blends[43]
Silvestri et al.2007poly(ethylene-co-vinyl alcohol)[44]
α-tocopherolFaizal et al.2008α-tocopherol methacrylate, acrylonitrile[46]
Faizal et al.2008α-tocopherol methacrylate, divinylbenzene, polysulfone, cellulose acetate and nylon supports[47]
Faizal et al.2009polysulfone and calix[4]resorcarenes[48]
(S)-5-benzylhydantoinLu et al.2007poly(styrene-stat-acrylonitrile-stat-vinyl-2,4-diamino-1,3,5-triazine[15]
BSAZhang et al.2010acrylamide, multi walled carbon nanotubes[31]
cholesterolSreenivasan et al.1998hydroxyethyl methacrylate[28]
cimetidineCeolin et al.2009methacrylic acid, hydroxyethyl methacrylate[24]
enrofloxacinKamel et al.2011methacrylic acid, 2-vinylpyridine[62]
folic acidDonato et al.2010acrylonitrile, acrylamide[49]
ibuprofenKochkodan et al.2010dimethylaminoethyl methacrylate, trimethylopropane trimethacrylate[90]
luteolinZhang et al.20093-aminopropyltriethoxysilane[55]
lysozymeChen et al.2010acrylamide, N,N-methylene-bis-acrylamide[58]
methyl orangeTakagishi et al.1972polyethyleneimine[3]
naproxenMa et al.2010poly(lactide-co-glycolide) and poly(D,L-lactide)[50]
naringinTrotta et al.2002acrylic acid, acrylonitrile[56]
Tasselli et al.2008acrylonitrile, itaconic acid, acrylic acid, acrylamide[40]
Ma et al.2011chitosan[16]
N-ethyl-o/p-toluensulfonamideGugliuzza et al.2007co-poly-(ether/amide)[9]
De Luca et al.2009co-poly-(ether/amide)[10]
oleanolic acidZhang et al.2011polyamide-6, poly(styrene-co-maleic acid)[53]
phosphatidylcolineSilvestri et al.2007poly(ethylene-co-vinyl alcohol)[44]
Pegoraro et al.2008poly(ethylene-co-vinyl alcohol)[45]
propanololYoshimatsu et al.2008poly(ethylene terephthalate)[19]
Jantarat et al.2008methacrylic acid[17]
Yoshimatsu et al.2008poly(ethylene terephthalate)[19]
Renkecz et al.2011methacrylic acid[60]
propofolPetcu et al.20044-acetoxystytrene[59]
puerarinQuin et al.2011acrylonitrile, acrylic acid[52]
rhodamine bMalaisamy et al.2004cellulose acetate, polysulfone[38]
Ulbricht et al.2005cellulose acetate, sulfonated polysulfone[36]
rutinZeng et al.2012acrylamide, 2-vinylpyridine, divinylbenzene[27]
sulfadiazineAlmeida et al.2011poly(vinyl chloride)[64]
sulfamethoxazoleAlmeida et al.2011poly(vinyl chloride)[64]
tetracyclineTrotta et al.2005acrylonitrile, acrylic acid[42]
Guerreiro et al.2011methacrylic acid, acrylamide[63]
theophyllineKobayashi et al.1995acrylonitrile, acrylic acid[32]
Wang et al.1996acrylonitrile, acrylic acid[5]
Wang et al.1997N,N-diethylaminodithiocarbamoylmethylstyrene, acrylic acid[33]
Kobayashi et al.1998acrylonitrile, acrylic acid[34]
Hattori et al.2004methacrylic acid, cellulose[56]
Silvestri et al.2006methyl methacrylate, methacrylic acid[43]
trimethoprimFan et al.2009methacrylic acid, polysulfone[29]
Rebelo et al.2011methacrylic acid, 2-vinylpyridine[61]
uric acidSilvestri et al.2006acrylonitrile, acrylic acid[43]
Aminoacids, Nucleotides And Sugars
alanineYu et al.2000acrylic acid[25]
AMPZayats et al.2002acrylamide, 3-(acrylamido)phenylboronic acid, N,N-methylene-bis-acrylamide, N,N,N',N'-tetramethylethylenediamine[23]
Sallacan et al.2002acrylamide-acrylamidephenylboronic acid copolymer[79]
5-benzylhydantoinLu et al.2007poly(styrene-stat-acrylonitrile-stat-vinyl-2,4-diamino-1,3,5-triazine)[15]
CMPZayats et al.2002acrylamide, 3-(acrylamido)phenylboronic acid, N,N-methylene-bis-acrylamide, N,N,N',N'-tetramethylethylenediamine[23]
Sallacan et al.2002acrylamide-acrylamidephenylboronic acid copolymer[79]
9-ethyladenineYoshikawa et al.2001polystyrene resin, cellulose acetate, polysulfone[78]
fructoseSallacan et al.2002acrylamide, acrylamidephenylboronic acid[79]
galactoseSallacan et al.2002acrylamide, acrylamidephenylboronic acid[79]
glucoseSallacan et al.2002acrylamide, acrylamidephenylboronic acid[79]
glutamic acidYoshikawa et al.1998carboxylated polysulfone[67]
Yoshikawa et al.1998chloromethylated polystyrene resin, divinylbenzene, dicyclohexylcarbodiimide[66]
Yu et al.2000methacrylic acid[25]
Yoshikawa et al.2007carboxylated polysulfone[18]
Yoshikawa et al.2007myrtenal polysulfone[74]
Sueyoshi et al.2010cellulose acetate[76]
Hatanaka et al.2011polyureas[75]
Sueyoshi et al.2012aldehydic polysulfone[77]
glutamineYoshikawa et al.1998chloromethylated polystyrene resin, divinylbenzene, dicyclohexylcarbodiimide[66]
Reddy et al.2002nylon-6[37]
GMPZayats et al.2002acrylamide, 3-(acrylamido)phenylboronic acid, N,N-methylene-bis-acrylamide, N,N,N',N'-tetramethylethylenediamine[23]
Sallacan et al.2002acrylamide-acrylamidephenylboronic acid copolymer[79]
leucineYoshikawa et al.1998chloromethylated polystyrene resin, divinylbenzene, dicyclohexylcarbodiimide[66]
lysineYoshikawa et al.1998chloromethylated polystyrene resin, divinylbenzene, dicyclohexylcarbodiimide[66]
NAD+, NADP+, NADH, NADPHPogorelova et al.2003acrylamide-acrylamidophenylboronic acid[80]
phenylalaninePark et al.2002acrylic acid[13]
Takeda et al.2005nylon-6, nylon-6,6, terephthalic phenylene polyamide[70]
Ul-Haq et al.2008carboxylated polysulfone[72]
Wu et al.2009sodium alginate, 3-aminopropyltriethoxysilane[30]
Ul-Haq et al.2010acrylonitrile, acrylic acid[73]
serineSon et al.2007polysulfone[71]
tryptophanYoshikawa et al.1997DLDE derivative[65]
Yu et al.2000acrylic acid, methacrylic acid[25]
Itou et al.2008polystyrene resin[68]
tyrosineDzgoev et al.19991,1,1-tris(hydroxymethyl)propane trimethacrylate, methacrylic acid[69]
Yu et al.2000acrylic acid, methacrylic acid[25]
UMPSallacan et al.2002acrylamide-acrylamidephenylboronic acid copolymer[79]
uracilWang et al.2004acrylonitrile, methacrylic acid[39]
Kobayashi et al.2008poly(styrene-co-maleic anhydride), poly(styrene-co-maleic acid)[41]
Metal Ions
[Ni-dipyridyl]2+ complexWang et al.2008N-vinyl-2-pyrrolidone[83]
Ag+Shawky et al.2009chitosan[86]
Wang et al.2009chitosan, poly(vinylalcohol)[87]
Cr(NO3)3·9H2OChen et al.2010sodium alginate, poly(vinylalcohol)[84]
Cu2+Li et al.2007nitrocellulose, poly(vinyl alcohol)[81]
Zhuqing et al.2010N-[3-(trimethoxysilyl) propyl]ethylenediamine[20]
metallothioneinCai et al.2008TiO2[21]
Ni(II)Vatanpour et al.2011methacrylic acid[85]
Zn(II)-(2,2'-bipyridyl)Zhai et al.20084-vinylpyridine[82]
Herbicides, Pesticides And Pollutants
ametrexPogorelova et al.2002acrylamide, sodium methacrylate, N,N-methylene-bis-acrylamide[93]
atranexPogorelova et al.2002acrylamide, sodium methacrylate, N,N-methylene-bis-acrylamide[93]
atrazineSergeyeva et al.2008methacrylic acid, itaconic acid, acrylamide[98]
Prasad et al.2007methacrylic acid,[91]
bisphenol ABryjak et al.2011polysulfone[100]
chlorpyrifosXie et al.2010polyaminothiophenol[22]
Cu(II)–catechol–urocanicSergeyeva et al.2010(tri)ethyleneglycoldimethacrylate and oligourethaneacrylate[102]
2,4-DPrasad et al.2007methacrylic acid[91]
desmetrynKochkodan et al.20012-acrylamido-2-methyl-1-propane sulfonic acid, N,N-methylene-bis-acrylamide[97]
Kochkodan et al.20102-acrylamido-2-methyl-1-propane sulfonic acid, N,N-methylene-bis-acrylamide[90]
diazinonPrasad et al.2007methacrylic acid,[91]
dibenzofuranKobayashi et al.2002polysulfone[35]
2,4-dichlorophenoxy acetic acidAyela et al.20074-vinylpyridine, trimethylacrylate[96]
Xie et al.2010polypyrrole polymers[95]
dichlorovosPrasad et al.2007methacrylic acid[91]
dimethoateDonato et al.2011acrylonitrile, methacrylic acid, acrylamide[89]
disulfotonPrasad et al.2007methacrylic acid[91]
ethionPrasad et al.2007methacrylic acid[91]
haloacetic acidsSuedee et al.20044-vinylpyridine[94]
4,4'-methylenedianilineDe Luca et al.2011acrylonitrile, acrylic acid[11]
Del Blanco et al.2012acrylonitrile, itaconic acid, acrylic acid, methacrylic acid[99]
monocrotophosZhu et al.2006methacrylic acid, Nylon-6[88]
N-benzyl-isopropylamineKalim et al.2005poly(vinyl alcohol), cellulose acetate[101]
parathionPrasad et al.2007methacrylic acid,[91]
phoratePrasad et al.2007methacrylic acid,[91]
pinacolyl methylphosphonateVishnuvardhan et al.2007methylmethacrylic acid[92]
prometrexPogorelova et al.2002acrylamide, sodium methacrylate, N,N-methylene-bis-acrylamide[93]
prozinexPogorelova et al.2002acrylamide, sodium methacrylate, N,N-methylene-bis-acrylamide[93]
simanexPogorelova et al.2002acrylamide, sodium methacrylate, N,N-methylene-bis-acrylamide[93]
terbutexPogorelova et al.2002acrylamide, sodium methacrylate, N,N-methylene-bis-acrylamide[93]
1,3,5-triazineKochkodan et al.20012-acrylamido-2-methyl-1-propane sulfonic acid, N,N-methylene-bis-acrylamide[97]
2,4,6-trichlorophenolFeng et al.20084-vinylpyridine, methyacrylic acid[26]
tyllanexPogorelova et al.2002acrylamide, sodium methacrylate, N,N-methylene-bis-acrylamide[93]
2,4,5-twerePrasad et al.2007methacrylic acid[91]

4. Conclusions

Molecular imprinting membranes appears to be one of the most promising separation and recognition technologies in terms of discrimination and versatility.

Moreover, the great number of polymers and techniques currently available allow the preparation of a large set of membranes with different functional groups and recognition sites, thus extending the application of such technology as proven by the number of papers reported by the literature in the past year.

Nomenclature

AAacrylic acid
AAmacrylamide
AIBN2,2'-azobisisobutyronitrile
AMPadenosine 5'-monophosphate
ANacrylonitrile
APTES3-aminopropyltriethoxysilane
α-TMAα-tocopherol methacrylate
Boc-N-α-tert-butoxycarbonyl protection
Bzlbenzyl protection
CAcellulose acetate
CMPcytosine 5'-monophosphate
CSchitosan
DLDEH-Asp(OcHex)-Leu-Asp(OcHex)-Glu(OBzl)-CH2-
DMFN,N'-dimethylformamide
DMSOdimethylsulfoxide
EGDMAethylene glycol dimethacrylate
ESDelectrospray deposition
EVApoly(ethylene-co-vinyl alcohol)
Glnglutamine
Gluglutamic acid
Glyglycine
GMPguanosine 5'-monophosphate
IAitaconic acid
iniferterinitiator-transfer agent-terminator
IPNinterpenetrating polymer
ISFETion sensitive field-effect transistor
Leuleucine
Lyslysine
MAAmethacrylic acid
MBAAN,N-methylene-bis-acrylamide
MIMmolecularly imprinted membrane
MIPmolecularly imprinted polymer
MIPCMmolecular imprinted polymer composite membrane
MMAmethylmethacrylic acid
NAD+/NADHnicotinamide adenine dinucleotide/reduced nicotinamide adenine dinucleotide
NADP+/NADPHnicotinamide adenine dinucleotide phosphate/reduced nicotinamide adenine dinucleotide phosphate
NGnaringin
NHDneohesperidin
NMIMnon molecularly imprinted membrane
NMIPnon molecularly imprinted particle
NMPN,N-methylpyrrolidone
Nynylon
P(AN-co-AA)poly(acrylonitrile-co-acrylic acid)
P(AN-co-AAm)poly(acrylonitrile-co-acrylamide)
P(AN-co-DTCS)poly(acrylonitrile-co-N,N'-diethylaminodithiocarbamoylmethylstyrene)
P(AN-co-IA)poly(acrylonitrile-co-itaconic acid)
P(AN-co-MAA)poly(acrylonitrile-co-methacrylic acid)
PA6polyamide-6
PANpolyacrylonitrile
PCphosphatidylcoline
PEGpolyethylene glycol
PETpoly(ethylene terephthalate)
Phephenylalanine
PPpoly(propylene)
PSfpolysulfone
PSMApoly(styrene-co-maleic acid)
PTFEpolytetrafluoroethylene
PUpolyurethane
PVApoly(vinyl alcohol)
PVCpoly(vinyl chloride)
PVDFpolyvinylidene fluoride (PVDF_phil: hydrophilized polyvinylidene fluoride; PVDF_phob: unmodified hydrophobic polyvinylidene fluoride)
QCMquartz crystal microbalance
RTrutin
SAsodium alginate
ScCO2supercritical carbon dioxide
Serserine
TCHtetracycline hydrochloride
TEOStetraethoxysilane
THFtetrahydrofuran
TMPtrimethoprim
Trptryptophan
Tyrtyrosine
UMPuridine 5'-monophosphate
VPvinylpyridine

Acknowledgments

The authors thank Claudio Baggiani (University of Torino) for useful discussions.

References

  1. Polyakov, M.V. Adsorption properties and structure of silica gel. Zhurnal fizicheskoi khimii 2 S. 1931, 799–804. [Google Scholar]
  2. Wulff, G.; Sarhan, A. Über die Anwendung von Enzymanalog Gebauten Polymeren zur Racemattrennung. Angew. Chem. 1972, 84, 364–365. [Google Scholar] [CrossRef]
  3. Takagishi, T.; Klotz, I.M. Macromolecule-small interactions: Introduction of additional binding sites in polyethyleneimine by disulfide cross-linkages. Biopolymers 1972, 11, 483–491. [Google Scholar] [CrossRef]
  4. Vasapollo, G.; Del Sole, R.; Mergola, L.; Lazzoi, M.R.; Scardino, A. Molecularly imprinted polymers: Present and future prospective. Int. J. Mol. Sc. 2011, 12, 5908–5945. [Google Scholar] [CrossRef]
  5. Wang, H.Y.; Kobayashi, T.; Fujii, N. Molecular imprint membranes prepared by the phase inversion precipitation technique. Langmuir 1996, 12, 4850–4856. [Google Scholar] [CrossRef]
  6. Varanasi, V.K. Molecularly imprinted polymers: The way forward. Organic Chem. Current Res. 2012, 1, 1–2. [Google Scholar]
  7. Haupt, K.; Mosbach, K. Molecularly imprinted polymers and their use in biomimetic sensors. Chem. Rev. 2000, 100, 2495–2504. [Google Scholar] [CrossRef]
  8. Yan, H.; Row, K.H. Characteristic and synthetic approach of molecularly imprinted polymer. Int. J. Mol. Sci. 2006, 7, 155–178. [Google Scholar] [CrossRef]
  9. Gugliuzza, A.; De Luca, G.; Tocci, E.; De Lorenzo, L.; Drioli, E. Intermolecular Interactions as Controlling Factor for Water Sorption into Polymer Membranes. J. Phys. Chem. B 2007, 111, 8868–8878. [Google Scholar] [CrossRef]
  10. De Luca, G.; Gugliuzza, A.; Drioli, E. Competitive hydrogen-bonding interactions in modified polymer membranes: A density functional theory investigation. J. Phys. Chem. B 2009, 113, 5473–5477. [Google Scholar] [CrossRef]
  11. De Luca, G.; Donato, L.; García Del Blanco, S.; Tasselli, F.; Drioli, E. On the cause of controlling affinity to small molecules of imprinted polymeric membranes prepared by noncovalent approach: A computational and experimental investigation. J. Phys. Chem. B 2011, 115, 9345–9351. [Google Scholar]
  12. Salam, A.; Ulbricht, M. Effect of surface modification on the synthesis of pore-filling polymeric monoliths in microfiltration membranes made from poly(propylene) and poly(ethylene terephthalate). Macromol. Mater. Eng. 2007, 292, 310–318. [Google Scholar] [CrossRef]
  13. Park, J.K.; Seo, J.I. Characteristics of Phe imprinted membrane prepared by the wet phase inversion method. KoreanJ. Chem. Eng. 2002, 19, 940–948. [Google Scholar] [CrossRef]
  14. Widawski, G.; Rawiso, B.; François, B. Self-organized honeycomb morphology of star-polymer polystyrene films. Nature 1994, 369, 387–389. [Google Scholar]
  15. Lu, Y.; Zhao, B.; Ren, Y.; Xiao, G.; Wang, X.; Li, C. Water-assisted formation of novel molecularly imprinted polymer membranes with ordered porous structure. Polymer 2007, 48, 6205–6209. [Google Scholar] [CrossRef]
  16. Ma, X.; Chen, R.; Zheng, X.; Youn, H.; Chen, Z. Preparation of molecularly imprinted CS membrane for recognizing naringin in aqueous media. Polym. Bull. 2011, 66, 853–863. [Google Scholar] [CrossRef]
  17. Jantarat, C.; Tangthong, N.; Songkro, S.; Martin, G.P.; Suedee, R. S-propranolol imprinted polymer nanoparticle-on-microsphere composite porous cellulose membrane for the enantioselectively controlled delivery of racemic propranolol. Int. J. Pharm. 2008, 349, 212–225. [Google Scholar] [CrossRef]
  18. Yoshikawa, M.; Nakai, K.; Matsumoto, H.; Tanioka, A.; Guiver, M.D.; Robertson, G.P. Molecularly imprinted nanofiber membranes from carboxylated polysulfone by electrospray deposition. Macromol. Rapid Commun. 2007, 28, 2100–2105. [Google Scholar] [CrossRef]
  19. Yoshimatsu, K.; Ye, L.; Lindberg, J.; Chronakis, I.S. Selective molecular adsorption using electrospun nanofiber affinity membranes. Biosens. Bioelectron. 2008, 23, 1208–1215. [Google Scholar] [CrossRef]
  20. Zhuqing, W.; Min, W.; Genhua, W.; Yuyong, S.; Chiyang, H. Ion imprinted sol-gel nanotubes membrane for selective separation of copper ion from aqueous solution. Microchim. Acta 2010, 169, 195–200. [Google Scholar] [CrossRef]
  21. Cai, Z.F.; Dai, H.J.; Si, S.H.; Ren, F.L. Molecular imprinting and adsorption of metallothionein on nanocrystalline titania membranes. Appl. Surf. Sci. 2008, 254, 4457–4461. [Google Scholar] [CrossRef]
  22. Xie, C.; Gao, S.; Guo, Q.; Xu, K. Electrochemical sensor for 2,4-dichlorophenoxy acetic acid using molecularly imprinted polypyrrole membrane as recognition element. Microchim. Acta 2010, 169, 145–152. [Google Scholar] [CrossRef]
  23. Zayats, M.; Lahav, M.; Kharitonov, A.B.; Willner, I. Imprinting of specific molecular recognition sites in inorganic and organic thin layer membranes associated with ion-sensitive field-effect transistors. Tetrahedron 2002, 58, 815–824. [Google Scholar] [CrossRef]
  24. Ceolin, G.; Navarro-Villoslada, F.; Moreno-Bondi, M.C.; Horvai, G.; Horvath, V. Accelerated development procedure for molecularly imprinted polymers using membrane filterplates. J. Comb. Chem. 2009, 11, 645–652. [Google Scholar] [CrossRef]
  25. Yu, C.; Mosbach, K. Influence of mobile phase composition and cross-linking density on the enantiomeric recognition properties of molecularly imprinted polymers. J. Chromatogr. A 2000, 888, 63–72. [Google Scholar] [CrossRef]
  26. Feng, Q.Z.; Zhao, L.X.; Chu, B.L.; Yan, W.; Lin, J.M. Synthesis and binding site characteristics of 2,4,6-trichlorophenol-imprinted polymers. Anal. Bioanal. Chem. 2008, 392, 1419–1429. [Google Scholar] [CrossRef]
  27. Zeng, H.; Wang, Y.; Liu, X.; Kong, J.; Nie, C. Preparation of molecular imprinted polymers using bi-functional monomer and bi-crosslinker for solid-phase extraction of rutin. Talanta 2012, 93, 172–181. [Google Scholar] [CrossRef]
  28. Sreenivasan, K. Synthesis and evaluation of a molecularly imprinted polyurethane-poly(HEMA) semi-interpenetrating polymer networks as membrane. J. Appl. Polym. Sci. 1998, 70, 19–22. [Google Scholar] [CrossRef]
  29. Fan, P.; Wang, B. Preparation of molecularly imprinted polymer membrane with blending trimethoprim-MIP and polysulfone and its transport properties Korean. J. Chem. Eng. 2009, 26, 1813–1820. [Google Scholar]
  30. Wu, H.; Zhao, Y.; Nie, M.; Jiang, Z. Molecularly imprinted organic-inorganic hybrid membranes for selective separation of Phe isomers and its analogue. Sep. Purif. Technol. 2009, 68, 97–104. [Google Scholar] [CrossRef]
  31. Zhang, M.; Huang, J.; Yu, P.; Chen, X. Preparation and characteristics of protein molecularly imprinted membranes on the surface of multiwalled carbon nanotubes. Talanta 2010, 81, 162–166. [Google Scholar] [CrossRef]
  32. Kobayashi, T.; Wang, H.Y.; Fujii, N. Molecular imprinting of theophylline in acrylonitrile-acrylic acid copolymer membrane. Chem. Lett. 1995, 24, 927–928. [Google Scholar]
  33. Wang, H.Y.; Kobayashi, T.; Fujii, N. Surface molecular imprinting on photosensitive dithiocarbamoyl polyacrylonitrile membranes using photograft polymerization. J. Chem. Tech. Biotechnol. 1997, 70, 355–362. [Google Scholar] [CrossRef]
  34. Kobayashi, T.; Wang, H.Y.; Fujii, N. Molecular imprint membranes of polyacrylonitrile copolymers with different acrylic acid segments. Anal. Chim. Acta 1998, 365, 81–88. [Google Scholar] [CrossRef]
  35. Kobayashi, T.; Reddy, P.S.; Ohta, M.; Abe, M.; Fujii, N. Molecularly imprinted polysulfone membranes having acceptor sites for donor dibenzofuran as novel membrane adsorbents: Charge transfer interaction as recognition origin. Chem. Mater. 2002, 14, 2499–2505. [Google Scholar] [CrossRef]
  36. Ulbricht, M.; Malaisamy, R. Insights into the mechanism of molecular imprinting by immersion precipitation phase inversion of polymer blends via a detailed morphology analysis of porous membranes. J. Mater. Chem. 2005, 15, 1487–1497. [Google Scholar] [CrossRef]
  37. Reddy, P.S.; Kobayashi, T.; Abe, M.; Fujii, N. Molecular imprinted Nylon-6 as a recognition material of amino acids. Eur. Polym. J. 2002, 38, 521–529. [Google Scholar] [CrossRef]
  38. Malaisamy, R.; Ulbricht, M. Evaluation of molecularly imprinted polymer blend filtration membranes under solid phase extraction conditions. Sep. Purif. Technol. 2004, 39, 211–219. [Google Scholar] [CrossRef]
  39. Wang, H.Y.; Xia, S.L.; Sun, H.; Liu, Y.K.; Cao, S.K.; Kobayashi, T. Molecularly imprinted copolymer membranes functionalized by phase inversion imprinting for uracil recognition and permselective binding. J. Chromatogr. B 2004, 804, 127–134. [Google Scholar] [CrossRef]
  40. Tasselli, F.; Donato, L.; Drioli, E. Evaluation of molecularly imprinted membranes based on different acrylic copolymers. J. Membrane Sci. 2008, 320, 167–172. [Google Scholar] [CrossRef]
  41. Kobayashi, T.; Leong, S.S.; Zhang, Q. Using polystyrene-co-maleic acid for molecularly imprinted membranes prepared in supercritical carbon dioxide. J. Appl. Polym. Sci. 2008, 108, 757–768. [Google Scholar] [CrossRef]
  42. Trotta, F.; Baggiani, C.; Luda, M.P.; Drioli, E.; Massari, T. A molecular imprinted membrane for molecular discrimination of tetracycline hydrochloride. J. Membrane Sci. 2005, 254, 13–19. [Google Scholar] [CrossRef]
  43. Silvestri, D.; Barbani, N.; Cristallini, C.; Giusti, P.; Ciardelli, G. Molecularly imprinted membranes for an improved recognition of biomolecules in aqueous medium. J. Membrane Sci. 2006, 282, 284–295. [Google Scholar] [CrossRef]
  44. Silvestri, D.; Barbani, N.; Coluccio, M.L.; Pegoraro, C.; Giusti, P.; Cristallini, C.; Ciardelli, G. poly(Ethylene-co-vinyl alcohol) membranes with specific adsorption properties for potential clinical application. Separ. Sci. Technol. 2007, 42, 2829–2847. [Google Scholar] [CrossRef]
  45. Pegoraro, C.; Silvestri, D.; Ciardelli, G.; Cristallini, C.; Barbani, N. Molecularly imprinted poly(ethylene-co-vinyl alcohol) membranes for the specific recognition of phospholipids. Biosens. Bioelectron. 2008, 24, 748–755. [Google Scholar] [CrossRef]
  46. Faizal, C.K.M.; Hoshina, Y.; Kobayashi, T. Scaffold membranes for selective adsorption of α-tocopherol by phase inversion covalently imprinting technique. J. Membrane Sci. 2008, 322, 503–511. [Google Scholar] [CrossRef]
  47. Faizal, C.K.M.; Kobayashi, T. Tocopherol-targeted membrane adsorbents prepared by hybrid molecular imprinting. Polym. Eng. Sci. 2008, 48, 1085–1093. [Google Scholar] [CrossRef]
  48. Faizal, C.K.M.; Kikuchic, Y.; Kobayashi, T. Molecular imprinting targeted for α-tocopherol by calix[4]resorcarenes derivative in membrane scaffold prepared by phase inversion. J. Membrane Sci. 2009, 334, 110–116. [Google Scholar] [CrossRef]
  49. Donato, L.; Tasselli, F.; Drioli, E. Molecularly imprinted membranes with affinity properties for folic acid. Separ. Sci. Technol. 2010, 45, 2273–2279. [Google Scholar] [CrossRef]
  50. Ma, D.; McHugh, A.J. The interplay of membrane formation and drug release in solution-cast films of polylactide polymers. Int. J. Pharm. 2010, 388, 1–12. [Google Scholar] [CrossRef]
  51. Saljoughi, E.; Amirilargani, M.; Mohammadi, T. Asymmetric cellulose acetate dialysis membranes: Synthesis, characterization, and performance. J. Appl. Polym. Sci. 2010, 116, 2251–2259. [Google Scholar]
  52. Quin, P.; Jie, Y.; Kairm, M.N. Characterization and selectivity studies of molecular imprinted membranes of puerarin using scanning electron microscopy. Scanning 2011, 33, 7–12. [Google Scholar] [CrossRef]
  53. Zhang, Q.; Zhang, X.; Zhang, W.; Pan, J.; Liu, L.; Zhang, H.; Zhao, D.; Li, Z. Preparation and adsorption properties of PA6/PSMA-OA molecularly imprinted composite membranes in supercritical CO2. Bull. Korean Chem. Soc. 2011, 32, 3348–3354. [Google Scholar] [CrossRef]
  54. Hattori, K.; Hiwatari, M.; Iiyama, C.; Yoshimi, Y.; Kohori, F.; Sakai, K.; Piletsky, A.A. Gate effect of theophylline-imprinted polymers grafted to the cellulose by living radical polymerization. J. Membrane Sci. 2004, 233, 169–173. [Google Scholar] [CrossRef]
  55. Zhang, Y.; Xiang, L.; Zhang, Y.; Gao, X. Study on preparation of composite membrane with molecular recognizing property and its selective permeance mechanism. Sep. Purif. Technol. 2009, 65, 130–136. [Google Scholar] [CrossRef]
  56. Trotta, F.; Drioli, E.; Baggiani, C.; Lacopo, D. Molecular imprinted polymeric membrane for naringin recognition. J. Membrane Sci. 2002, 201, 77–84. [Google Scholar] [CrossRef]
  57. Donato, L.; Chiappetta, G.; Drioli, E. Surface functionalization of PVDF membrane with a naringin-imprinted polymer layer using photo-polymerization method. Separ. Sci. Technol. 2011, 46, 1555–1562. [Google Scholar] [CrossRef]
  58. Chen, R.R.; Qin, L.; Jia, M.; He, X.W.; Li, W.Y. Novel surface modified molecularly imprinted membrane prepared with iniferter for permselective separation of lysozyme. J. Membrane Sci. 2010, 363, 212–220. [Google Scholar] [CrossRef]
  59. Petcu, M.; Schaare, P.N.; Cook, C.J. Propofol-imprinted membranes with potential application in biosensors. Analy. Chim. Acta 2004, 504, 73–79. [Google Scholar] [CrossRef]
  60. Renkecz, T.; Ceolin, G.; Horvàth, V. Selective solid phase extraction of propranolol on multiwell membrane filter plates modified with molecularly imprinted polymer. Analyst 2011, 136, 2175–2182. [Google Scholar] [CrossRef]
  61. Rebelo, T.S.C.R.; Almeida, S.A.A.; Guerreiro, J.R.L.; Montenegro, M.C.B.S.M.; Sales, M.G.F. Trimethoprim-selective electrodes with molecularly imprinted polymers acting as ionophores and potentiometric transduction on graphite solid-contact. Microchem. J. 2011, 98, 21–28. [Google Scholar] [CrossRef]
  62. Kamel, A.H.; Moreira, F.T.C.; Rebelo, T.S.C.R.; Sales, M.G.F. Molecularly-imprinted materials for potentiometric transduction: Application to the antibiotic enrofloxacin. Anal. Lett. 2011, 44, 2107–2123. [Google Scholar] [CrossRef]
  63. Guerreiro, J.R.L.; Freitas, V.; Sales, M.G.F. New sensing materials of molecularly-imprinted polymers for the selective recognition of chlortetracycline. Microchem. J. 2011, 97, 173–181. [Google Scholar] [CrossRef]
  64. Almeida, S.A.A.; Moreira, F.T.C.; Heitor, A.M.; Montenegro, M.C.B.S.M.; Aguilar, G.G.; Sales, M.G.F. Sulphonamide-imprinted sol-gel materials as ionophores in potentiometric transduction. Mater. Sci. Eng. C 2011, 31, 1784–1790. [Google Scholar] [CrossRef]
  65. Yoshikawa, M.; Izumi, J.; Kitao, T.; Sakamoto, S. Alternative molecularly imprinted polymeric membranes from a tetrapeptide residue consisting of D- or L-amino acids. Macromol. Rapid Commun. 1997, 18, 761–767. [Google Scholar] [CrossRef]
  66. Yoshikawa, M.; Fujisawa, T.; Izumi, J.; Kitao, T.; Sakamoto, S. Molecularly imprinted polymeric membranes involving tetrapeptide EQKL derivatives as chiral-recognition sites toward amino acids. Anal.Chim. Acta 1998, 365, 59–67. [Google Scholar] [CrossRef]
  67. Yoshikawa, M.; Izumi, J.; Ooi, T.; Kitao, T.; Guiver, M.D.; Robertson, G.P. Carboxylated polysulfone membranes having a chiral recognition site induced by an alternative molecular imprinting technique. Polym. Bull. 1998, 40, 517–524. [Google Scholar] [CrossRef]
  68. Itou, Y.; Nakano, M.; Yoshikawa, M. Optical resolution of racemic amino acid derivatives with molecularly imprinted membranes from tetrapetide consisting of glycinyl residues. J. Membrane Sci. 2008, 325, 371–375. [Google Scholar] [CrossRef]
  69. Dzgoev, A.; Haupt, K. Enantioselective molecularly imprinted polymer membranes. Chirality 1999, 11, 465–469. [Google Scholar] [CrossRef]
  70. Takeda, K.; Abe, M.; Kobayashi, T. Molecular-imprinted nylon membranes for the permselective binding of phe as optical- resolution membrane adsorbents. J. Appl. Polym. Sci. 2005, 97, 620–626. [Google Scholar] [CrossRef]
  71. Son, S.H.; Jegal, J. Chiral Separation of D,L-serine racemate using a molecularly imprinted polymer composite membrane. J. Appl. Polym. Sci. 2007, 104, 1866–1872. [Google Scholar] [CrossRef]
  72. Ul-Haq, N.; Khan, T.; Park, J.K. Enantioseparation with D-Phe- and L-Phe-imprinted PAN-based membranes by ultrafiltration. J. Chem. Technol. Biotechnol. 2008, 83, 524–533. [Google Scholar] [CrossRef]
  73. Ul-Haq, N.; Park, J.K. Chiral resolution of Phe by D-Phe imprinted membrane considering rejection property. Bioprocess Biosyst. Eng. 2010, 33, 79–86. [Google Scholar] [CrossRef]
  74. Yoshikawa, M.; Murakoshi, K.; Kogita, T.; Hanaoka, K.; Guiver, M.D.; Robertson, G.P. Chiral separation membranes from modified polysulfone having myrtenal-derived terpenoid side groups. Eur. Polym. J. 2006, 42, 2532–2539. [Google Scholar] [CrossRef]
  75. Hatanaka, M.; Nishioka, Y.; Yoshikawa, M. Polyurea with L-lysinyl residues as components: Application to membrane separation of enantiomers. Macromol. Chem. Phys. 2011, 212, 1351–1359. [Google Scholar] [CrossRef]
  76. Sueyoshi, T.; Fukushima, C.; Yoshikawa, M. Molecularly imprinted nanofiber membranes from cellulose acetate aimed for chiral separation. J. Membrane Sci. 2010, 357, 90–97. [Google Scholar] [CrossRef]
  77. Sueyoshi, Y.; Utsunomiya, A.; Yoshikawa, M.; Robertson, G.P.; Guiver, M.D. Chiral separation with molecularly imprinted polysulfone-aldehyde derivatized nanofiber membranes. J. Membr. Sci. 2012, 401–402, 89–96. [Google Scholar] [CrossRef]
  78. Yoshikawa, M.; Izumi, J.; Guiver, M.D.; Robertson, G.P. Recognition and selective transport of nucleic acid components through molecularly imprinted polymeric membranes. Macromol. Mater. Eng. 2001, 286, 52–59. [Google Scholar] [CrossRef]
  79. Sallacan, N.; Zayats, M.; Bourenko, T.; Kharitonov, A.B.; Willner, I. Imprinting of nucleotide and monosaccharide recognition sites in acrylamidephenylboronic acid-AAm copolymer membranes associated with electronic transducers. Anal. Chem. 2002, 74, 702–712. [Google Scholar]
  80. Pogorelova, S.P.; Zayats, M.; Bourenko, T.; Kharitonov, A.B.; Lioubashevski, O.; Katz, E.; Willner, I. Analysis of NAD(P)+/NAD(P)H cofactors by imprinted polymer membranes associated with ion-sensitive field-effect transistor devices and Au–quartz crystals. Anal. Chem. 2003, 75, 509–517. [Google Scholar]
  81. Li, Z.M.; Liu, J.M.; Liu, Z.B.; Liu, Q.Y.; Lin, X.; Li, F.M.; Yang, M.L.; Zhu, G.H.; Huang, X.M. Preparation for nitrocellulose membrane-poly (vinyl alcohol)-ionic imprinting and its application to determine trace copper by room temperature phosphorimetry. Anal. Chim. Acta 2007, 589, 44–50. [Google Scholar] [CrossRef]
  82. Zhai, Y.; Liu, Y.; Chang, X.; Ruan, X.; Liu, J. Metal ion-small molecule complex imprinted polymer membranes: Preparation and separation characteristics. React. Funct. Polym. 2008, 68, 284–291. [Google Scholar] [CrossRef]
  83. Wang, X.J.; Xu, Z.L.; Bing, N.C.; Yang, Z.G. Preparation and characterization of metal-complex imprinted PVDF hollow fiber membranes. J. Appl. Polym. Sci. 2008, 109, 64–73. [Google Scholar] [CrossRef]
  84. Chen, J.H.; Li, G.P.; Liu, Q.L.; Ni, J.C.; Wu, W.B.; Lin, J.M. Cr(III) ionic imprinted polyvinyl alcohol/sodium alginate (PVA/SA) porous composite membranes for selective adsorption of Cr(III) ions. Chem. Eng. J. 2010, 165, 465–473. [Google Scholar]
  85. Vatanpour, V.; Madaeni, S.S.; Zinadini, S.; Rajabi, H.R. Development of ion imprinted technique for designing nickel ion selective membrane. J. Membrane Sci. 2011, 373, 36–42. [Google Scholar] [CrossRef]
  86. Shawky, H.A. Synthesis of ion-imprinting chitosan/PVA crosslinked membrane for selective removal of Ag(I). J. Appl. Polym. Sci. 2009, 114, 2608–2615. [Google Scholar] [CrossRef]
  87. Wang, X.; Zhang, L.; Ma, C.; Song, R.; Hou, H.; Li, D. Enrichment and separation of silver from waste solutions by metal ion imprinted membrane. Hydrometallurgy 2009, 100, 82–86. [Google Scholar] [CrossRef]
  88. Zhu, X.; Su, Q.; Cai, J.; Yang, J.; Gao, Y. Molecularly imprinted polymer membranes for substance-selective solid-phase extraction from aqueous solutions. J. Appl. Polym. Sci. 2006, 101, 4468–4473. [Google Scholar] [CrossRef]
  89. Donato, L.; Greco, M.C.; Drioli, E. Preparation of molecularly imprinted membranes and evaluation of their performance in the selective recognition of dimethoate. Desalination and Water Treatment 2011, 30, 171–177. [Google Scholar]
  90. Kochkodan, V.; Hilal, N.; Melnik, V.; Kochkodan, O.; Vasilenko, O. Selective recognition of organic pollutants in aqueous solutions with composite imprinted membranes. Advan. Colloid Interface Sci. 2010, 159, 180–188. [Google Scholar] [CrossRef]
  91. Prasad, K.; Prathish, K.P.; Gladis, J.M.; Naidu, G.R.; Rao, T.P. Design and development of imprinted polymer inclusion membrane-based field monitoring device for trace determination of phorate (O,O-Diethyl S-Ethyl Thiomethyl Phophorodithioate)in Natural Waters. Electroanalysis 2007, 19, 1195–1200. [Google Scholar] [CrossRef]
  92. Vishnuvardhan, V.; Prathish, K.P.; Naidu, G.R.K.; Prasada Rao, T. Fabrication and topographical analysis of non-covalently imprinted polymer inclusion membranes for the selective sensing of pinacolyl methylphosphonate—A simulant of soman. Electrochim. Acta 2007, 52, 6922–6928. [Google Scholar]
  93. Pogorelova, S.P.; Bourenko, T.; Kharitonov, A.B.; Willner, I. Selective sensing of triazine herbicides in imprinted membranes using ion-sensitive field-effect transistors and microgravimetric quartz crystal microbalance measurements. Analyst 2002, 127, 1484–1491. [Google Scholar] [CrossRef]
  94. Suedee, R.; Srichana, T.; Sangpagai, C.; Tunthana, C.; Vanichapichat, P. Development of trichloroacetic acid sensor based on molecularly imprinted polymer membrane for the screening of complex mixture of haloacetic acids in drinking water. Anal. Chim. Acta 2004, 504, 89–100. [Google Scholar] [CrossRef]
  95. Xie, C.; Li, H.; Li, S.; Wu, J.; Zhang, Z. Surface Molecular Self-assembly for organophosphate pesticide imprinting in electropolymerized poly(p-aminothiophenol) membranes on a gold nanoparticle modified glassy carbon electrode. Anal. Chem. 2010, 82, 241–249. [Google Scholar]
  96. Ayela, C.; Vandevelde, F.; Lagrange, D.; Haupt, K.; Nicu, L. Combining resonant piezoelectric micromembranes with molecularly impronte polymers. Angew. Chem. Int. Ed. 2007, 46, 9271–9274. [Google Scholar]
  97. Kochkodan, V.; Weigel, W.; Ulbricht, M. Thin layer molecularly imprinted microfiltration membranes by photofunctionalization using a coated a-cleavage photoinitiator. Analyst 2001, 126, 803–809. [Google Scholar] [CrossRef]
  98. Sergeyeva, T.A.; Piletska, O.V.; Piletsky, S.A.; Sergeeva, L.M.; Brovko, O.O.; El’ska, G.V. Data on the structure and recognition properties of the template-selective binding sites in semi-IPN-based molecularly imprinted polymer membranes. Mater. Sci. Eng. C 2008, 28, 1472–1479. [Google Scholar] [CrossRef]
  99. Del Blanco, S.G.; Donato, L.; Drioli, E. Development of molecularly impronte membranes for selective recognition of primary amines in organic medium. Sep. Purif. Technol. 2012, 87, 40–46. [Google Scholar] [CrossRef]
  100. Bryjak, M.; Duraj, I. Molecularly imprinted membranes for removal of bisphenol A. Solvent Extr. Ion Exch. 2011, 29, 432–439. [Google Scholar] [CrossRef]
  101. Kalim, R.; Schomäcker, R.; Yüce, S.; Brüggemann, O. Catalysis of α-elimination applying membranes with incorporated molecularly imprinted polymer particles. Polym. Bull. 2005, 55, 287–297. [Google Scholar] [CrossRef]
  102. Sergeyeva, T.A.; Slinchenko, O.A.; Gorbach, L.A.; Matyushov, V.F.; Brovko, O.O.; Piletsky, S.A.; Sergeeva, L.M.; Elsk, G.V. Catalytic molecularly imprinted polymer membranes: Development of the biomimetic sensor for phenols detection. Anal. Chim. Acta 2010, 659, 274–279. [Google Scholar] [CrossRef]
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