Molecularly Imprinted Polymer Particles Research Articles

An Overview of Microfluidic‐assisted Strategies for Synthesis and Applications of Molecularly Imprinted Polymers

This review gives an overview of using microfluidics in conjunction with molecularly imprinted polymers (MIP), which covers two aspects: on the one hand, on‐chip synthesis of polymer and MIP particles on the nano and the micro scale. This comprises both approaches using two different immiscible solvents and homogeneous matrices to obtain the desired particle morphologies. On the other hand, especially paper‐based microfluidic systems have attracted increasing interest as low‐cost analytical tools that are inherently useful for applying at the point of care. By now, there have been several successful attempts to combine them with MIP (instead of biological recognition systems) and to successfully apply them in environmental samples, food matrices, and for diagnostic applications.

3D inkjet printing of hybrid electroactive ink based on molecularly imprinted polymers for lipopolysaccharides detection

A hybrid electroactive ink based on molecularly imprinted polymer (MIP) hollow microparticles, zinc oxide nanoparticles (ZnO NPs) and conductive carbon paste (CP) is reported herein for the first time. The MIP/ZnO NPs/CP and corresponding non-imprinted NIP/ZnONPs/CP modified inks were screen-printed on plastic substrates via 3D inkjet technology to cover around 40 working screen-printed carbon electrodes (SPCE) pieces in a single batch. The custom-made electrochemical MIP/ZnONPs/CP@SPCE sensor was designed for the detection of bacterial endotoxins, i.e., lipopolysaccharides (LPS), derived from Pseudomonas aeruginosa. Hollow MIP silica microparticles with specific properties for 3D printing application, in terms of granulation and morphology, were synthesized via sol-gel method using tetraethyl orthosilicate and (3-aminopropyl) triethoxysilane as monomers. Following the structural and morphological characterization of microparticles, the evaluation of template rebinding indicated a clear specificity of MIPs for LPS compared to the NIPs. Hybrid MIP/ZnONPs/CP and NIP/ZnONPs/CP inks were characterized using morphological and structural methods, which confirmed a viscosity of 25.000 mPa.s, a granulation of <20 µm, and a solid powder content of <27 %, as well as a homogenous incorporation of MIP particles and ZnONPs in the conductive CP. Finally, the electrochemical evaluation of the modified MIP/ZnONPs/CP@SPCE sensor revealed a good sensitivity to LPS molecules in PBS at pH 7.4, in the linear working range 1 - 100 µM, where a 0.058 µM limit of detection (LOD) and a response time less than or equal to 1 min were determined. The selectivity of the MIP/ZnONPs/CP@SPCE sensor towards LPS from Salmonella enterica and Escherichia coli was also assessed, highlighting a clear difference between these structural resembling species.

Efficient synthesis of the undiluted vegetable juice-compatible hydrophilic quantum dot-labeled fluorescent molecularly imprinted polymer microspheres via facile one-pot surface-initiated ARGET ATRP

The development of fluorescent molecularly imprinted polymers (MIPs) applicable for herbicide optosensing in the undiluted vegetable juices is highly important for food safety control, but still remains a challenging task. Herein, we report on a facile and efficient new strategy for the synthesis of hydrophilic quantum dot (QD)-labeled fluorescent MIP microspheres capable of directly and selectively optosensing a widely used herbicide (i.e., 2,4-dichlorophenoxyacetic acid, 2,4-D) in the undiluted vegetable juices. Such fluorescent MIP particles were readily prepared through one-step grafting of a red CdTe QD-labeled 2,4-D-MIP layer with hydrophilic polyethylene glycol brushes onto the preformed uniform “living” polymer microspheres (with surface-bound alkyl halide groups) via one-pot surface-initiated activator regenerated by electron transfer (ARGET) atom transfer radical polymerization (ATRP) (SI-ARGET ATRP). They proved to be a highly useful optosensor with high 2,4-D selectivity and sensitivity (the limit of detection ≤ 0.14 μM) in the undiluted Chinese cabbage and cucumber juices. They also showed excellent photostability and reusability and could be directly utilized for 2,4-D detection with high recoveries (98.2 %-102.4 %) and accuracy (RSD≤3.8 %) in the undiluted Chinese cabbage and cucumber juices at three spiking levels of both 2,4-D and its mixtures with several analogues. The use of SI-ARGET ATRP significantly reduced the applied copper catalyst concentration (about 5 μM), which greatly alleviated the quenching effect of the copper catalyst on the fluorescence of the QD-labeled MIP (usually observed for those prepared via normal ATRPs that typically use several hundreds of μM of copper catalysts), thus making this facile new strategy highly efficient for developing advanced fluorescent MIPs that hold much promise in various bioanalytical and diagnostic applications.

Preparation of a surface molecularly imprinted thermo-sensitive polymer for selective trypsin capture

Molecularly imprinted polymers (MIPs) are innovative porous materials created through polymerization templating methods for highly selective, sensitive detection and separation of the desired chemical species, known as template molecules. Surface imprinting over nano-sized substrates with special functional groups is an effective approach for improving the mass transfer and rebinding capacity. In this study, we successfully performed surface imprinting using methacrylic acid (MAA) and thermoresponsive N-isopropyl acrylamide (NIPAm) as functional monomers on acrylic-functionalized silica nanoparticles and served as a Trypsin artificial receptor. The resulting Trypsin imprinted polymer exhibited a binding capacity of 1022.44 mg/g, surpassing the non-imprinted polymer’s capacity of 292.41 mg/g within 45 min. Moreover, the imprinting factor, the main influence factor in MIP performance, was 3.5, demonstrating the significant selectivity of the polymeric products. In addition, due to the temperature sensitivity of NIPAm the template removing process was simply done by changing pore size. The silica nanoparticles and the synthesized MIP particles had diameters of approximately 95 nm and 105 nm, respectively, with the polymer layer thickness being around 5 nm. The MIP adsorption model followed the Freundlich isotherm and pseudo-second-order kinetics resulting in efficiencies of 93.0 % and 95.4 %, respectively. The developed Trypsin imprinted polymer was reusable for four consecutive uses,demonstrating both resilience and selectivity towards Trypsin.

Electrochemical Detection of Pseudomonas aeruginosa Quorum Sensing Molecule (S)-N-Butyryl Homoserine Lactone Using Molecularly Imprinted Polymers.

Pseudomonas aeruginosa is a multidrug-resistant Gram-negative bacterium that poses a significant threat to public health, necessitating rapid and on-site detection methods for rapid recognition. The goal of the project is therefore to indirectly detect the presence of P. aeruginosa in environmental water samples targeting one of its quorum-sensing molecules, namely, (S)-N-butyryl homoserine lactone (BHL). To this aim, molecularly imprinted polymers (MIPs) were synthesized via bulk free-radical polymerization using BHL as a template molecule. The obtained MIP particles were immobilized onto screen-printed electrodes (MIP-SPEs), and the BHL rebinding was analyzed via electrochemical impedance spectroscopy (EIS). To study the specificity of the synthesized MIPs, isotherm curves were built after on-point rebinding analysis performed via LC-MS measurements for both MIPs and NIPs (nonimprinted polymers, used as a negative control), obtaining an imprinting factor (IF) of 2.8 (at C f = 0.4 mM). The MIP-SPEs were integrated into an electrochemical biosensor with a linear range of 1 × 101-1 × 103 nM and a limit of detection (LoD) of 31.78 ± 4.08 nM. Selectivity measurements were also performed after choosing specific interferent molecules, such as structural analogs and potential interferents, followed by on-point analysis performed in spiked tap water to prove the sensor's potential to detect the presence of the quorum-sensing molecule in environmentally related real-life samples.

Malathion Detection Using Molecularly-Imprinted Polymer Quartz Crystal Microbalance Sensor

The extensive use of pesticides can result in overexposure and soil, water, and produce residues. For instance, residues of malathion were found on some vegetables. Molecularly-imprinted polymers (MIP) have been recently developed for sensing of pesticide residues. This study prepared malathion-imprinted polymers via precipitation polymerization and deposited on quartz crystal microbalance (QCM) electrodes. FTIR spectroscopy proved the incorporation and removal of malathion in the matrix of MIP. SEM images revealed that MIP particles are larger than the non-imprinted polymer (NIP) particles due to the incorporation of malathion. Binding experiments were done using standard malathion solutions of 10 to 60 ppm. The MIP-QCM sensor had a greater response than the NIP-QCM sensor. This is due to the specific binding sites in the MIP matrix. On the other hand, the response of NIP-QCM sensor is attributed to the non-specific adsorption sites in its matrix. A sensitivity and detection limit of 1.62 Hz·L/mg and 5.67 ppm, respectively were determined for the MIP-QCM sensor. Lastly, the MIP-QCM sensor is stable and reusable up to three (3) cycles.

Microwave‐assisted molecularly imprinted polymer synthesis for chemometric and rebinding mechanism of drug release applications

AbstractSynthesis of molecularly imprinted polymers (MIP) has gained wide interest as drug delivery vehicles in recent years. The conventional one‐variable‐at‐a‐time method for determining the best formulation ratio of MIP templates is resource‐ and time‐consuming. Thus, this study focused on the response surface methodology optimization of the best formulation for MIP preparation using methacrylic acid and divinylbenzene as functional monomer and cross‐linker, respectively. Two preparation systems were studied, namely microwave (MW)‐assisted and conventional synthesis. The MIPs showed spherical particles with smaller particle sizes (500 nm–1.45 μm) and higher yields (0.5–1.2 g) via MW‐assisted synthesis as compared to the conventional synthesis (size 660 nm–3.65 μm, yield 0.5–1.15 g). MW‐assisted synthesis is faster and more efficient to synthesize controlled shapes and sizes of MIP particles. The rebinding properties of prepared MIP via MW were higher (7.15 ± 0.02 mg/g) than conventional synthesis (3.00 ± 0.31 mg/g). The empirical models were developed to correlate the output response of rebinding properties and input variables. The analysis of variance confirmed that experimental data were superbly fitted to the proposed response models. A satisfactory correlation between the experimental and predicted values was obtained by both MIP prepared via MW‐assisted and conventional synthesis.

A molecularly imprinted polymer for microextraction by packed sorbent of sulfonylureas herbicides from corn samples

A molecularly imprinted polymer (MIP) was synthesized and assessed as a selective extraction phase in the microextraction by packed sorbent (MEPS) of sulfonylureas herbicides (SUHs) — Thifensulfuron, Chlorosulfuron, Tribenuron, and Bensulfuron — from grounded corn samples. Bensulfuron was employed as the template for the MIP preparation. MIP particles were chemically and structurally characterized. Distribution (Kd), selectivity (k), and relative selectivity (k') coefficients were estimated using binary mixtures of bensulfuron/betazon and bensulfuron/prometon. The most significant parameters affecting the MEPS performance were systematically studied in univariate and multivariate experiments. Analyses were performed by liquid chromatography coupled to time-of-flight mass spectrometry (LC-ToF). Under selected conditions, the developed MIP-MEPS-LC-ToF method demonstrated suitable analytical confidence and reliability. Determination coefficients (r2) higher than 0.9940, and limits of detection (LODs) of 2.5 µg kg-1 were obtained. Intra- and interday precision was lower than 14.2%, and accuracy ranged between 89.6% and 113.6%. The synthesized MIP demonstrated enhanced selectivity and higher SUHs uptake capability compared to the non-imprinted polymer (NIP) and tested commercial sorbents. Besides, the method is a cheap, feasible, and environmentally friendly analytical tool. A single MEPS device packed with 1.0 mg of MIP was reused more than 180 times without loss in its extraction capabilities.

Dipstick Sensor Based on Molecularly Imprinted Polymer‐Coated Screen‐Printed Electrodes for the Single‐Shot Detection of Glucose in Urine Samples—From Fundamental Study toward Point‐of‐Care Application

AbstractGlucose biosensors play an extremely important role in health care systems worldwide. Therefore, the field continues to attract significant attention leading to the development of innovative technologies. Due to their characteristics, Molecularly Imprinted Polymers (MIPs) represent a promising alternative to commercial enzymatic sensors. In this work, a low‐cost, flexible MIP‐based platform for glucose sensing by integrating MIP particles directly into screen‐printed electrodes (SPEs) is realized. The sensor design allows the detection of glucose via two different transducer principles, the so‐called “heat‐transfer method” (HTM) and electrochemical impedance spectroscopy (EIS). The sensitivity and selectivity of the sensor are demonstrated by comparing the responses obtained toward three different saccharides. Furthermore, the application potential of the MIP‐SPE sensor is demonstrated by analyzing the response in urine samples, showing a linear range of 14.38–330 µm with HTM and 1.37–330 µm with EIS. To bring the sensor closer to a real life application, a handheld dipstick sensor is developed, allowing the single‐shot detection of glucose in urine using EIS. This study illustrates that the simplicity of the dipstick readout coupled with the straightforward manufacturing process opens up the possibility for mass production, making this platform a very attractive alternative to commercial glucose sensors.

Direct analysis of tobacco specific nitrosamines in tobacco products using a molecularly imprinted polymer-packed column.

Tobacco specific nitrosamines (TSNAs) are highly carcinogenic by-products in tobacco samples, and their presence is regulated by the Food and Drug Administration. Molecularly imprinted polymers (MIPs) are synthetic polymers that have been "imprinted" with a template analyte in a co-polymer system, and can selectively extract analytes from complex matrices. MIPs can be incorporated into online systems, replacing traditional high performance liquid chromatography (HPLC) columns. MIP material specific for TSNAs was packed into an empty HPLC column using a slurry packing technique. The developed method with the MIP-packed HPLC column was validated on a LC-MS/MS system for the quantitation of N-nitrosonornicotine (NNN) and 4- (methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) in commercial tobacco products. The method was linear over .1-10 ng/ml (.4-10 μg/g) for NNN and NNK. The limit of detection (LOD) was .03 ng/ml (12 μg/g) and the limit of quantitation (LOQ), .1 ng/ml (.4 μg/g). All column uniformity parameters with the exception of theoretical plate number were within the accepted criteria (% RSD values <15%). Theoretical plate number was <250, owing to the large (50 μm) sized MIP particles. Twenty-six tobacco products contained TSNA concentrations that were consistent with reported literature values. The TSNA-MIP based HPLC column effectively replaced a traditional reverse phase HPLC column, and was used for the direct analysis of nicotine and tobacco products without extensive sample preparation prior to instrumental analysis.

Thermal Pyocyanin Sensor Based on Molecularly Imprinted Polymers for the Indirect Detection of Pseudomonas aeruginosa

Pseudomonas aeruginosa is a ubiquitous multi-drug-resistant bacterium, capable of causing serious illnesses and infections. This research focuses on the development of a thermal sensor for the indirect detection of P. aeruginosa infection using molecularly imprinted polymers (MIPs). This was achieved by developing MIPs for the detection of pyocyanin, the main toxin secreted by P. aeruginosa. To this end, phenazine was used as a dummy template, evaluating several polymeric compositions to achieve a selective MIP for pyocyanin recognition. The sensitivity of the synthesized MIPs was investigated by UV-vis analysis, with the best composition having a maximum rebinding capacity of 30 μmol g-1 and an imprinting factor (IF) of 1.59. Subsequently, the MIP particles were immobilized onto planar aluminum chips using an adhesive layer, to perform thermal resistance measurements at clinically relevant concentrations of pyocyanin (1.4-9.8 μM), achieving a limit of detection (LoD) of 0.347 ± 0.027 μM. The selectivity of the sensor was also scrutinized by subjecting the receptor to potential interferents. Furthermore, the rebinding was demonstrated in King's A medium, highlighting the potential of the sensor for the indirect detection of P. aeruginosa in complex fluids. The research culminates in the demonstration of the MIP-based sensor's applicability for clinical diagnosis. To achieve this goal, an experiment was performed in which the sensor was exposed to pyocyanin-spiked saliva samples, achieving a limit of detection of 0.569 ± 0.063 μM and demonstrating that this technology is suitable to detect the presence of the toxin even at the very first stage of its production.

A Molecularly Imprinted Polymer-Based Thermal Sensor for the Selective Detection of Melamine in Milk Samples.

In recent years, melamine-sensing technologies have increasingly gained attention, mainly due to the misuse of the molecule as an adulterant in milk and other foods. Molecularly imprinted polymers (MIPs) are ideal candidates for the recognition of melamine in real-life samples. The prepared MIP particles were incorporated into a thermally conductive layer via micro-contact deposition and its response towards melamine was analyzed using the heat-transfer method (HTM). The sensor displayed an excellent selectivity when analyzing the thermal response to other chemicals commonly found in foods, and its applicability in food safety was demonstrated after evaluation in untreated milk samples, demonstrating a limit of detection of 6.02 μM. As the EU/US melamine legal limit in milk of 2.5 mg/kg falls within the linear range of the sensor, it can offer an innovative solution for routine screening of milk samples in order to detect adulteration with melamine. The results shown in this work thus demonstrate the great potential of a low-cost thermal platform for the detection of food adulteration in complex matrices.

Facile Fabrication of Hollow Molecularly Imprinted Polymer Particles with Multicore Structure via Miniemulsion Polymerization

Facile Fabrication of Hollow Molecularly Imprinted Polymer Particles with Multicore Structure via Miniemulsion Polymerization

An ultra-sensitive and highly selective impedimetric sensor for vitamin D measurement based on a novel imprinted polymer synthesized utilizing template-derived functional monomer

A novel vitamin D3-imprinted (VD)-polymer was synthesized utilizing a functional monomer derived from vitamin D3. Acryloyl chloride reacted with VD leading to a functional monomer capable of interaction with VD during the molecularly imprinted polymer (MIP) synthesis step. Vitamin D3-derived functional monomer and divinylbenzene were copolymerized in the presence of vitamin D3 in order to create a new MIP, holding VD selective cavities, after template (VD) removal from the polymer. The MIP nanoparticles were used for the modification of a carbon paste electrode to fabricate VD selective sensor. The charge transfer resistance of Fe(CN)63-/Fe(CN)64−couple for the MIP-modified electrode increased significantly in the presence of VD; whereas, the non-imprinted polymer (NIP)-CPE electrode was not affected by VD, suggesting well acting of recognition sites of the MIP nanoparticles, incorporated into the electrode. The sensing mechanism was attributed to a gate effect principle. Interring of VD molecules to the selective sites of the MIP nanoparticles, existing on the electrode surface, makes the MIP particles swell and this leads to blocking the majority of routes via which the probe electroactive species accesses the carbon particles at the electrode surface. The MIP electrode was not sensitive to some molecules structurally similar to VD, suggesting a highly selective nature of the designed sensor. The new VD sensor impedimetric response as a function of the logarithm of VD concentration was found to be linear in the range of 1.0–100.0 pM. The detection limit of the sensor was estimated to be 0.22 pM. The sensor was used for VD level estimation in plasma samples.

Modern and Dedicated Methods for Producing Molecularly Imprinted Polymer Layers in Sensing Applications

Molecular imprinting (MI) is the most available and known method to produce artificial recognition sites, similar to antibodies, inside or at the surface of a polymeric material. For this reason, scholars all over the world have found MI appealing, thus developing, in this past period, various types of molecularly imprinted polymers (MIPs) that can be applied to a wide range of applications, including catalysis, separation sciences and monitoring/diagnostic devices for chemicals, biochemicals and pharmaceuticals. For instance, the advantages brought by the use of MIPs in the sensing and analytics field refer to higher selectivity, sensitivity and low detection limits, but also to higher chemical and thermal stability as well as reusability. In light of recent literature findings, this review presents both modern and dedicated methods applied to produce MIP layers that can be integrated with existent detection systems. In this respect, the following MI methods to produce sensing layers are presented and discussed: surface polymerization, electropolymerization, sol–gel derived techniques, phase inversionand deposition of electroactive pastes/inks that include MIP particles.

A highly sensitive plastic optic-fiber with a molecularly imprinted polymer coating for selective detection of 4-chlorophenol in water

To realize the selective detection of 4-chlorophenol (4-CP) in water, a highly sensitive plastic optical fiber (POF) evanescent wave sensor was prepared using a D-shaped POF coated selective adsorption film of 4-CP. The film was composed of molecularly imprinted polymer (MIP) particles and PEBA2533 matrix. The MIP particles were employed to realize the selective adsorption and enrichment of 4-CP molecules, which lead to the changes in the refractive index of the MIP-PEBA2533 coating. These, in turn, resulted in changes in the light transmission in the D-shaped region and caused the attenuation of the evanescent field intensity on the surface of the sensing region. To illustrate the measurement principle, a theoretical model of the sensor was established. Furthermore, the performance parameters of the sensors, such as sensitivity, repeatability, selectivity and low limit of detection (LOD), were experimentally studied. The results highlighted that the proposed sensor exhibited a good sensitivity of -0.56 × 10-6 (μg/L)-1 and LOD of 100 μg/L for the detection of 4-CP in water. Moreover, this optic-fiber sensor has high specific recognition ability for 4-CP. The results of this study could inform the development of methods for on-line and accurate detection of 4-CP.

Thermal Detection of Glucose in Urine Using a Molecularly Imprinted Polymer as a Recognition Element.

Glucose bio-sensing technologies have received increasing attention in the last few decades, primarily due to the fundamental role that glucose metabolism plays in diseases (e.g., diabetes). Molecularly imprinted polymers (MIPs) could offer an alternative means of analysis to a field that is traditionally dominated by enzyme-based devices, posing superior chemical stability, cost-effectiveness, and ease of fabrication. Their integration into sensing devices as recognition elements has been extensively studied with different readout methods such as quartz-crystal microbalance or impedance spectroscopy. In this work, a dummy imprinting approach is introduced, describing the synthesis and optimization of a MIP toward the sensing of glucose. Integration of this polymer into a thermally conductive receptor layer was achieved by micro-contact deposition. In essence, the MIP particles are pressed into a polyvinyl chloride adhesive layer using a polydimethylsiloxane stamp. The prepared layer is then evaluated with the so-called heat-transfer method, allowing the determination of the specificity and the sensitivity of the receptor layer. Furthermore, the selectivity was assessed by analyzing the thermal response after infusion with increasing concentrations of different saccharide analogues in phosphate-buffered saline (PBS). The obtained results show a linear range of the sensor of 0.0194–0.3300 mM for the detection of glucose in PBS. Finally, a potential application of the sensor was demonstrated by exposing the receptor layer to increasing concentrations of glucose in human urine samples, demonstrating a linear range of 0.0444–0.3300 mM. The results obtained in this paper highlight the applicability of the sensor both in terms of non-invasive glucose monitoring and for the analysis of food samples.

Encapsulation of Molecularly Imprinted Polymer Particles in Microcapsule by Facile Pickering Emulsion Polymerization

Encapsulation of Molecularly Imprinted Polymer Particles in Microcapsule by Facile Pickering Emulsion Polymerization

A rapid and sensitive method for separation of Cu2+ ions from industrial wastewater sample and water samples with methacrylamide-ethylene glycol dimethacrylate: A new synthesis of molecularly imprinted polymer.

In this study, new molecularly imprinted polymer particles (MIP) were synthesised to extract Cu2+ ions from aqueous solutions using radical polymerisation. MIP was developed using the methacrylamide‐ethylene glycol dimethacrylate (EGDMA) cross linking agent, methacrylamide monomer, and ACV initiator by the radical polymerisation method. A comparison of various cross linking agents in MIP production showed that the best cross linking agents are EGDMA and gallic acid. The template ions were removed by leaching with 0.100 M HCl. The polymer particles were characterised by FTIR spectroscopy, thermogravimetric analysis (TGA) and scanning electron microscopy (SEM). The effect of different parameters such as cross linkers, pH, time, maximum adsorption capacity, and kinetic and isotherm adsorption were investigated. The best conditions were determined (pH = 8.0, t = 10 min, and q m = 262.53 mg g−1). The adsorption data were best fitted by Freundlich isotherm and pseudo second order kinetic models, as well. Due to its high adsorption capacity and multi‐layer behaviour, this method is an easy, fast and safe way to extract cations. Removal of Cu2+ in certified tap water and rain water was demonstrated and the industrial wastewater sample (Charmshahr, Iran) with which the MIP was developed using Methacrylamide‐ Ethylene Glycol Dimethacrylate (EGDMA) was good enough for Cu2+ determination in matrices containing components with similar chemical property such as Co2+, Zn2+, Fe2.

Colorimetric Sensing of Amoxicillin Facilitated by Molecularly Imprinted Polymers.

The scope of the presented research orientates itself towards the development of a Molecularly Imprinted Polymer (MIP)-based dye displacement assay for the colorimetric detection of the antibiotic amoxicillin in aqueous medium. With this in mind, the initial development of an MIP capable of such a task sets focus on monolithic bulk polymerization to assess monomer/crosslinker combinations that have potential towards the binding of amoxicillin. The best performing composition (based on specificity and binding capacity) is utilized in the synthesis of MIP particles by emulsion polymerization, yielding particles that prove to be more homogenous in size and morphology compared to that of the crushed monolithic MIP, which is an essential trait when it comes to the accuracy of the resulting assay. The specificity and selectivity of the emulsion MIP proceeds to be highlighted, demonstrating a higher affinity towards amoxicillin compared to other compounds of the aminopenicillin class (ampicillin and cloxacillin). Conversion of the polymeric receptor is then undertaken, identifying a suitable dye for the displacement assay by means of binding experiments with malachite green, crystal violet, and mordant orange. Once identified, the optimal dye is then loaded onto the synthetic receptor, and the displaceability of the dye deduced by means of a dose response experiment. Alongside the sensitivity, the selectivity of the assay is scrutinized against cloxacillin and ampicillin. Yielding a dye displacement assay that can be used (semi-)quantitatively in a rapid manner.