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Moxifloxacin evaluation in pharmaceuticals and biological fluids is in high demand. It is important to fabricate a simple, sensitive, selective, miniaturized, and cost-effective chemical sensor to detect moxifloxacin in the environment. In this study, an electrochemical sensor based on molecularly imprinted polymer (MIP) was fabricated for the detection of moxifloxacin in which interdigital electrodes (IDEs) were used as transducers. Thermal free-radical bulk polymerization was used to synthesize MIP, methacrylic acid (MAA) was used as a functional monomer, ethylene glycol dimethacrylate (EGDMA) as a crosslinker, azobisisobutyronitrile (AIBN) as a free radical initiator, and dimethyl sulfoxide (DMSO) as a porogenic solvent in a poly (methacrylic acid) system for efficient recognition. The LCR meter was used to measure various electrical properties such as inductance and resistance. A concentration-dependent linear response was observed by the fabricated sensor having a lower limit of detection of 240 and 63 ppb for series and parallel resistance, respectively. Meanwhile, series and parallel inductance had lower detection limits of 48 and 8 ppb, respectively. Furthermore, in the presence of competing agents such as uric acid, ascorbic acid, and paracetamol, the fabricated sensor showed a selective response for moxifloxacin. The fabricated sensor also showed reversible and reproducible response. [ABSTRACT FROM AUTHOR]

Teicoplanin has been banned in the veterinary field due to the drug resistance of antibiotics. However, teicoplanin residue from the antibiotic abuse of humans and animals poses a threat to people's health. Therefore, it is necessary to develop an efficient way for the highly accurate and reliable detection of teicoplanin from humans, food, and water. In this study, novel imprinted quantum dots of teicoplanin were prepared based on boronate affinity-based precisely controlled surface imprinting. The imprinting factor (IF) for teicoplanin was evaluated and reached a high value of 6.51. The results showed excellent sensitivity and selectivity towards teicoplanin. The relative fluorescence intensity was inversely proportional to the concentration of teicoplanin, in the range of 1.0–17 μM. And its limit of detection (LOD) was obtained as 0.714 μM. The fluorescence quenching process was mainly controlled by a static quenching mechanism via the non-radiative electron-transfer process between QDs and the five-membered cyclic boronate esters. The recoveries for the spiked urine, milk, and water samples ranged from 95.33 to 104.17%, 91.83 to 97.33, and 94.22 to 106.67%, respectively. [ABSTRACT FROM AUTHOR]

In this paper, we developed a paper-based fluorescent sensor using functional composite materials composed of graphene quantum dots (GQDs) coated with molecularly imprinted polymers (MIPs) for the selective detection of tetracycline (TC) in water. GQDs, as eco-friendly fluorophores, were chemically grafted onto the surface of paper fibers. MIPs, serving as the recognition element, were then wrapped around the GQDs via precipitation polymerization using 3-aminopropyltriethoxysilane (APTES) as the functional monomer. Optimal parameters such as quantum dot concentration, grafting time, and elution time were examined to assess the sensor's detection performance. The results revealed that the sensor exhibited a linear response to TC concentrations in the range of 1 to 40 µmol/L, with a limit of detection (LOD) of 0.87 µmol/L. When applied to spiked detection in actual water samples, recoveries ranged from 103.3% to 109.4%. Overall, this paper-based fluorescent sensor (MIPs@GQDs@PAD) shows great potential for portable, multi-channel, and rapid detection of TC in water samples in the future. [ABSTRACT FROM AUTHOR]

A method was developed to fabricate a glassy carbon electrode with electrodeposited palladium particles and a molecularly imprinted polymer derived from nicotinamide. This approach enables the determination of dopamine in the presence of structurally related compounds. The incorporation of a polymer featuring specific recognition sites tailored to the template molecule significantly enhanced the sensitivity and selectivity of dopamine detection. The immobilization of palladium particles on the electrode surface further improved the selectivity of voltammetric dopamine determination, even in the presence of adrenaline and noradrenaline, which exhibited a 200 mV difference in oxidation peak potentials. The analytical signal showed a linear bilogarithmic dependence on dopamine concentration within the range 5.0 × 10–9 to 5.0 × 10–3 M. This method was successfully applied to an analysis of urine samples, demonstrating its practical utility in real-world applications. [ABSTRACT FROM AUTHOR]

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A novel graphene-modified molecularly imprinted polymer-based electrochemical sensor (MIP/RGO-GCE) was developed for the sensitive and selective detection of sibutramine in sports doping control. The sensor was fabricated by electropolymerizing o-phenylenediamine on a reduced graphene oxide-modified glassy carbon electrode in the presence of sibutramine as the template molecule. Under optimized conditions, the MIP/RGO-GCE sensor exhibited a wide linear range (0.05 to 20 μM), low detection limit (0.02 μM), high sensitivity (1.27 μA/μM), good precision (RSD < 2.7%), and long-term stability (93.5% retention after two weeks). The sensor's applicability was successfully demonstrated by analyzing spiked human urine and serum samples, with recoveries ranging from 95.8 to 103.2% and good agreement with the reference HPLC method. Furthermore, the sensor showed a rapid response time of 5 s and excellent reproducibility with an RSD of 1.5% for repeated measurements. The proposed sensor offers a rapid, cost-effective, and reliable alternative to traditional chromatographic methods for sibutramine detection in sports doping control. [ABSTRACT FROM AUTHOR]

A novel magnetic molecular-imprinted polymer (MMIP) was used to selectively extract folic acid directly from real samples. Folic acid was used as template molecule, Fe3O4/SiO2-3-triethoxysilyl-propyl-acrylamide as functional monomer, azobisisobutyronitrile as initiation, ethylene glycol dimethacrylate as crosslinker agent, and acrylamide as the secondary monomer in a mixed ethanol-water solvent. The effect of different parameters on the extraction efficiency was studied, and the optimum conditions were established as follows: the concentrations of crosslinking and template were fixed at 0.05 and 0.06 g, absorption percentage was 96.5, pH was adjusted to 8, and extraction time was 8 h with a temperature of 25 °C. By examining the effect of pH, we tried to investigate the effect of the amide groups that present in MMIP and its intermolecular hydrogen interaction with folic acid. After optimising the effective parameters in polymer synthesis and adsorption rate, a magnetic imprinting dispersive solid-phase extraction method combined with fluorescence spectrophotometry at λem = 367 nm (MMIP-DSPE-FL) was constructed for sensitive determination of folic acid in tomato samples. The limit of quantification (LOQ) and limit of detection (LOD) values were 30.00 ± 0.01 μg L−1 and 10.00 ± 0.03 μg L−1, respectively, after the MMIP-DSPE preconcentration. Three tomato samples were analysed to give recoveries in the range of 80.2–81.6%, with relative standard deviation values below 0.6% (n = 3). The prepared MMIP-DSPE showed high selectivity toward folic acid, which could be used six times without changing adsorption capacity. The adsorption isotherm of the folic acid-imprinted polymer pursued the Langmuir model (RL = 0.029), and the kinetics model followed pseudo-first-order (R 2 = 0.9974). [ABSTRACT FROM AUTHOR]

AbstractNanosurface-imprinted polymer nanoprobes (Fe3O4@MIP) were prepared by microwave synthesis using Fe3O4 as a nanosubstrate, aspirin as a template, α-methacrylic acid (MAA) as a functional monomer, ethylene glycol dimethacrylate (EGDMA) as a cross-linking agent, and 2,2'-azobisisobutyronitrile (AIBN) as an initiator. Characterization of Fe3O4@MIP revealed that the spectral probe exhibited strong resonance Rayleigh scattering (RRS) for aspirin. With the increase in aspirin concentration, the RRS energy transfer (RRS-ET) was enhanced, and the signal at 370 nm decreased, providing a linear range from 0.25 to 12.5 μmol/L and a detection limit (DL) of 0.08 μmol/L. The developed protocol was used for the determination of aspirin in drugs with recoveries from 93.2 to 102.6. [ABSTRACT FROM AUTHOR]

Molecularly imprinted polymers (MIPs) are synthetic polymers that mimic the functions of antibodies. Though MIPs are promising tools in various areas, achieving high selectivity in MIPs can be difficult. To improve selectivity, various approaches have been implemented; however, the role of polymerization methods or synthetic techniques in enhancing the selectivity of MIPs has not been studied and remains a crucial area for further research. MIPs are typically prepared from free radical reactions. Recently, we found that Dielectric Barrier Discharge (DBD) plasma can be used to initiate the polymerization of vinyl monomers. The DBD plasma method allows the monomers to associate with the template molecules and initiate polymerization with minimal disruption to the positioning of the monomers. We hypothesize that this could be a preferred method to prepare MIPs over the traditional radical reaction that may cause a disturbance of the pre-associated monomers on the templates for the polymerization. Chicken egg white serum albumin (CESA) was used as the template protein for the MIPs. Our results show that in all test conditions, approximately twofold improvement in selectivity was achieved, which is the primary performance metric for MIPs. This enhancement was evident across all categories, including MIPs prepared from various monomer combinations. [ABSTRACT FROM AUTHOR]

Owing to their potential to transform traditional medical diagnostics and health monitoring, wearable biosensors have become an alternative evolutionary technology in the field of medical care. However, it is still necessary to overcome some key technique challenges, such as the selectivity, sensitivity, and stability of biometric identification. Herein, a novel, wearable electrochemical sensor based on a molecularly imprinted polymer (MIP) integrated with a copper benzene-1,3,5-tricarboxylate metal–organic framework (MOF) was designed for the detection of stress through the on-body monitoring of cortisol in sweat. The MOF was used as the substrate for MIP deposition to enhance the stability and sensitivity of the sensor. The sensor consisted of two layers, with a microfluidic layer as the top layer for spontaneous sweating and a modified electrode as the bottom layer for sensing. The sensor measured cortisol levels by detecting the current change that occurred when the target molecules bound to the imprinted cavities, using Prussian blue nanoparticles embedded in the MIP framework as the REDOX probe. The proposed sensor exhibited a linear detection range of 0.01–1000 nM with a detection limit of 0.0027 nM, and favorable specificity over other analogies. This facile anti-body free sensor showed excellent stability, and can be successfully applied for in situ cortisol monitoring. [ABSTRACT FROM AUTHOR]

Transferrin (TRF), recognized as a glycoprotein clinical biomarker and therapeutic target, has its concentration applicable for disease diagnosis and treatment monitoring. Consequently, this study developed boronic acid affinity magnetic surface molecularly imprinted polymers (B-MMIPs) with pH-responsitivity as the "capture probe" for TRF, which have high affinity similar to antibodies, with a dissociation constant of (3.82 ± 0.24) × 10−8 M, showing 7 times of reusability. The self-copolymerized imprinted layer synthesized with dopamine (DA) and 3-Aminophenylboronic acid (APBA) as double monomers avoided nonspecific binding sites and produced excellent adsorption properties. Taking the gold nanostar (AuNS) with a branch tip "hot spot" structure as the core, the silver-coated AuNS functionalized with the biorecognition element 4-mercaptophenylboronic acid (MPBA) was employed as a surface-enhanced Raman scattering (SERS) nanotag (AuNS@Ag-MPBA) to label TRF, thereby constructing a double boronic acid affinity "sandwich" SERS biosensor (B-MMIPs-TRF-SERS nanotag) for the highly sensitive detection of TRF. The SERS biosensor exhibited a detection limit for TRF of 0.004 ng/mL, and its application to spiked serum samples confirmed its reliability and feasibility, demonstrating significant potential for clinical TRF detection. Moreover, the SERS biosensor designed in this study offers advantages in stability, detection speed (40 min), and cost efficiency. The portable Raman instrument for SERS detection fulfills the requirements for point-of-care testing. [ABSTRACT FROM AUTHOR]

An ultrasensitive and selective voltammetric platform combined a molecularly imprinted poly(pyrrole) membrane with Ag-nanoparticle-functionalized black phosphorus nanosheets (MIP/BPNS-AgNPs) was developed for trace GAT detection. The physicochemical properties of the MIP/BPNS-AgNPs were studied by various spectroscopic and electrochemical techniques. BPNS-AgNPs improved the ambient stability and electrochemical activity of the BPNS and possessed a large surface area for accommodating abundant templates to produce specific imprinted sites. The resulting MIP/BPNS-AgNP-modified glassy carbon electrode (GCE) greatly enhanced voltammetric responses for GAT. The MIP/BPNS-AgNP/GCE exhibited admirable GAT determination performance, with two linear responses (0.001–1 and 1–50 μM), high sensitivity (9.965 and 0.5378 μA μM−1), and a low detection limit of 0.2 nM. In addition, the MIP electrode could selectively detect GAT in complex matrices and retain roust responses for a month. The applicability of MIP/BPNS-AgNP/GCE toward the detection of GAT in pharmaceutical formulations, milk, and human serum was verified with satisfactory results.

Statins reduce cholesterol synthesis by inhibiting the enzyme hydroxymethylglutaryl-CoA (HMG-CoA) reductase. Rosuvastatin (ROS) is a statin drug used to prevent cardiovascular diseases and treat abnormal lipids. This study describes the design and fabrication of a nanomaterial-assisted molecularly imprinted polymer (MIP)-based electrochemical sensor for ROS determination. In addition, MIP-based electrochemical sensors were designed to detect ROS in both standard solutions and serum samples. In the MIP-based electrochemical sensor developed via the photopolymerization (PP) technique on the glassy carbon electrode (GCE) surface, were used zinc oxide nanoparticles (ZnO NPs) as a pore former, p-aminobenzoic acid (p-ABA) as functional monomer, ROS as template molecule. Electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and scanning electron microscopy (SEM) techniques were used to carry out detailed characterizations concerning surface morphology and electrochemistry. Under optimized experimental conditions, the linearity range of the designed sensor was found 1.0 × 10−13–1.0 × 10−12 M. The superior selectivity of the MIP-based sensor against ROS in the presence of their binary mixtures was confirmed by interference studies. The recovery rates of the MIP-based sensors were calculated as 100.35 % and 99.16 % in commercial tablet form and serum samples, respectively. Moreover, the proposed sensor's relative selectivity coefficient (k′) was calculated, and it provided good selectivity for ROS over the NIP sensor. In conclusion, this newly developed sensor offers an advantageous approach for selective, sensitive, rapid and cost-effective analysis of ROS from binary mixtures. Additionally, this study is the first electrochemical sensor using nanomaterial-assisted MIP technology for ROS analysis, and its sensitivity is higher than that of other studies in the literature.

Abstract The integration of advanced materials and photonic nanostructures can lead to enhanced biodetection capabilities, crucial in clinical scenarios and point‐of‐care diagnostics, where simplified strategies are essential. Herein, a molecularly imprinted polymer (MIP) photonic nanostructure is demonstrated, which selectively binding to transforming growth factor‐beta (TGF‐β), in which the sensing transduction is enhanced by bound states in the continuum (BICs). The MIP operating as a synthetic antibody matrix and coupled with BIC resonance, enhances the optical response to TGF‐β at imprinted sites, leading to an augmented detection capability, thoroughly evaluated through spectral shift and optical lever analogue readout. The validation underscores the MIP‐BIC sensor capability to detect TGF‐β in spiked saliva, achieving a limit of detection of 10 fM and a resolution of 0.5 pM at physiological concentrations, with a precision of two orders of magnitude above discrimination threshold in patients. The MIP tailored selectivity is highlighted by an imprinting factor of 52, showcasing the sensor resistance to interference from other analytes. The MIP‐BIC sensor architecture streamlines the detection process eliminating the need for complex sandwich immunoassays and demonstrates the potential for high‐precision quantification. This positions the system as a robust tool for biomarker detection, especially in real‐world diagnostic scenarios.

Abstract In this study, a sensitive and selective fluorescent chemosensor was developed for the determination of pirimicarb pesticide by adopting the surface molecular imprinting approach. The magnetic molecularly imprinted polymer (MIP) nanocomposite was prepared using pirimicarb as the template molecule, CuFe2O4 nanoparticles, and graphene quantum dots as a fluorophore (MIP-CuFe2O4/GQDs). It was then characterized using X-ray diffraction (XRD) technique, Fourier transforms infrared (FT-IR) spectroscopy, scanning electron microscope (SEM), and transmission electron microscopy (TEM). The response surface methodology (RSM) was also employed to optimize and estimate the effective parameters of pirimicarb adsorption by this polymer. According to the experimental results, the average particle size and imprinting factor (IF) of this polymer are 53.61 nm and 2.48, respectively. Moreover, this polymer has an excellent ability to adsorb pirimicarb with a removal percentage of 99.92 at pH = 7.54, initial pirimicarb concentration = 10.17 mg/L, polymer dosage = 840 mg/L, and contact time = 6.15 min. The detection of pirimicarb was performed by fluorescence spectroscopy at a concentration range of 0–50 mg/L, and a sensitivity of 15.808 a.u/mg and a limit of detection of 1.79 mg/L were obtained. Real samples with RSD less than 2 were measured using this chemosensor. Besides, the proposed chemosensor demonstrated remarkable selectivity by checking some other insecticides with similar and different molecular structures to pirimicarb, such as diazinon, deltamethrin, and chlorpyrifos.

Furosemide (FUR), banned in sports events by the World Anti‐Doping Agency, is a key target in drug tests, necessitating a pretreatment material capable of selectively, rapidly, and sufficiently separating/enriching analytes from complex matrices. Herein, a metal‐mediated magnetic molecularly imprinted polymer (mMIP) was rationally designed and synthesized for the specific capture of FUR. The preparations involved the utilization of chromium (III) as the binding pivot, (3‐aminopropyl)triethoxysilane as functional monomer, and Fe3O4 as core, all assembled via free radical polymerization. Both the morphologies and adsorptive properties of the mMIP were characterized using multiple methods. The resulting Cr(III)‐mediated mMIP (ChM‐mMIP) presented excellent selectivity and specificity toward FUR. Under optimized conditions, the adsorption capacity reached 128.50 mg/g within 10 min, and the imprinting factor was 10.41. Moreover, it was also successfully applied as a dispersive solid‐phase extraction material, enabling the detection of FUR concentration as low as 20 ng/mL in human urine samples when coupled with a high‐performance liquid chromatography/photodiode array. Overall, this study offers a valuable strategy for the development of novel recognition material. [ABSTRACT FROM AUTHOR]

Owing to the demand for chemical analysis of low concentrations of the Brilliant Green (BG) dye released into the environment, molecularly imprinted polymer (MIP) materials have been investigated for their use in SPME preconcentration devices. Thin coatings of MIP on solid supports allow fast adsorption of the analyte and higher selectivity of adsorption. Biosourced fibers of Posidonia oceanica (Pos) were taken as a the solid support to which a thin film of MIP was chemically attached. The material synthesis involved two steps: chemical grafting of methacrylate groups onto Pos by a silane coupling, and copolymerization with the free functional monomer and cross-linker in the presence of BG. Polymerization of the functional monomers methacrylic acid and acrylamide yielded the materials PosMAA@MIP and PosAA@MIP respectively. The strength of their interaction with BG and the stoichiometry of the pre-polymerization complex were assessed by 1H NMR experiments in DMSO-d6 solution. Characterization by IR spectroscopy and thermogravimetric analysis validated the successful syntheses. The points of zero charge were at pH 3.31 and 4.50 for PosMAA@MIP and PosAA@MIP, respectively, influencing the optimal adsorption of BG at pH 4. Kinetic studies revealed the rapid adsorption of more than 90% of the BG within 20 min. All MIPs exhibited higher adsorption capacity for BG compared to non-imprinted materials. PosAA@MIP showed the highest adsorption efficiency and selectivity, with an imprinting factor of 1.9. The thermodynamics of adsorption was studied by fitting the Langmuir–Volmer and Volmer models to the experimental data, from which the selective adsorption capacities of BG on PosMAA@MIP and PosAA@MIP were 289 and 313 µmol·g−1, respectively. Additionally, PosAA@MIP exhibited higher extraction efficiency for BG than for its metabolites eosin and methylene blue, underscoring its superior ability to selectively capture target molecules. [ABSTRACT FROM AUTHOR]

Chronic kidney disease (CKD) is one of the most serious non‐communicable diseases affecting the population. In the early‐stages patients have no obvious symptoms, until it becomes life‐threatening leading end‐stage kidney failure. Therefore, it is important to early diagnose CKD to allow therapeutic interventions and progression monitoring. Here, a point‐of‐care (POC) sensing platform is reported for the simultaneous detection of three CKD biomarkers, namely creatinine, urea, and human serum albumin (HSA), using reduced graphene oxide/polydopamine‐molecularly imprinted polymer (rGO/PDA‐MIP) fabricated with novel surface‐molecularly imprinting technology. A multi‐channel electrochemical POC readout system with differential pulse voltammetry (DPV) function is developed, allowing the simultaneous detection of the three biomarkers, in combination with the surface‐MIP electrodes. This sensing platform achieves the record low limit‐of‐detection (LoD) at a femtomolar level for all three analytes, with wide detection ranges covering their physiological concentrations. Clinical validation is performed by measuring these analytes in serum and urine from healthy controls and patients with CKD. The average recovery rate is 81.8–119.1% compared to the results obtained from the hospital, while this platform is more cost‐effective, user‐friendly, and requires less sample‐to‐result time, showing the potential to be deployed in resource‐limited settings for the early diagnosis and tracking progression of CKD. [ABSTRACT FROM AUTHOR]

Acne vulgaris, a prevalent skin condition, arises from an imbalance in skin flora, fostering bacterial overgrowth. Addressing this issue, clindamycin molecularly imprinted polymeric nanoparticles (Clin-MIP) loaded onto polyurethane nanofiber scaffolds were developed for acne treatment. Clin-MIP was synthesized via precipitation polymerization using methacrylic acid (MAA), ethylene glycol dimethacrylate (EGDMA), and azoisobutyronitrile (AIBN) as functional monomers, crosslinkers, and free-radical initiators, respectively. MIP characterization utilized Fourier-transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM) before being incorporated into polyurethane nanofibers through electrospinning. Further analysis involved FTIR, scanning electron microscopy (SEM), in vitro release studies, and an ex vivo study. Clin-MIP showed strong antibacterial activity against S. aureus, with inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values of 0.39 and 6.25 μg/mL, respectively. It significantly dropped the bacterial count from 1 × 108 to 39 × 101 CFU/mL in vivo and has bactericidal activity within 180 min of incubation in vitro. The pharmacodynamic and histopathology studies revealed a significant decrease in infected animal skin inflammation, epidermal hypertrophy, and congestion upon treatment with Clin-MIP polyurethane nanofiber and reduced pro-inflammatory cytokines (NLRP3, TNF-α, IL-1β, and IL-6) conducive to acne healing. Consequently, the recently created Clin-MIP polyurethane nanofibrous scaffold. This innovative approach offers insight into creating materials with several uses for treating infectious wounds caused by acne. [ABSTRACT FROM AUTHOR]

This research investigates the usage of pipette tip micro solid phase extraction for the separation of 6-mercaptopurine of complicated matrices before its spectrophotometric detection. To overcome the non-selectivity of spectrophotometry, an ethylene glycol dimethacrylatebased molecularly imprinted polymer was prepared and applied as an adsorbent, which enabled selective and fast extraction of the analyte. To improve the transfer of the analyte to the adsorbent, a salting-out effect was employed by the addition of 300 mg of NaCl to the sample before performing microextraction. Variables affecting the microextraction of the protocol were investigated utilizing two ways one-factorat-a-time and response surface methodology, which showed good consistency with each other. Extraction parameters were optimized as pH of sample = 9.0, sample volume = 10 ml, amount of adsorbent = 2.0 mg, eluent = 250 µl of methanol:acetonitrile (1:5 v/v), and extraction and elution cycles of 10 and 12 times, respectively. The dynamic linear range of the protocol was 1.0-1000.0 µg l-1, with a limit of detection of 0.25 µg l-1. The method was compared with extraction by a non-imprinted polymer. The extraction efficiency of the analyte was obtained from 96.0% to 99.8%, by relative standard deviations better than 5.3%. The suggested technique was employed to determine 6-mercaptopurine in seawater and body fluid samples, and the results were validated by comparing them to a standard HPLC method. The whole analysis time, including microextraction, was about 25 min and to perform this method, the sole instrument required is a conventional spectrophotometer. [ABSTRACT FROM AUTHOR]

Epitope imprinting has shown better prospects to synthesize synthetic receptors for proteins. Here, dual epitope imprinted polymer electrode (DEIP) matrix was fabricated on gold surface of electrochemical quartz crystal microbalance (EQCM) for recognition of target epitope sequence in blood samples of patients suffering from brain fever. Epitope sequences from outer membrane protein Por B of Neisseria meningitidis (MC58) bacteria predicted through immunoinformatic tools were chosen for imprinting. Self‐assembled monolayers (SAM) of cysteine appended epitope sequences on gold nanoparticles were subjected to polymerization prior to electrodeposition on gold coated EQCM electrode. The polymeric matrix was woven around the cysteine appended epitope SAMs through multiple monomers (3‐sulfo propyl methacrylate potassium salt (3‐SPMAP), benzyl methacrylate (BMA)) and crosslinker (N, N′‐methylene‐bis‐acrylamide). On extraction of the peptide sequences, imprinted cavities were able to selectively and specifically bind targeted epitope sequences in laboratory samples as well as 'real' samples of patients. Selectivity of sensor was examined through mismatched peptide sequences and certain plasma proteins also. The sensor was able to show specific binding towards the blood samples of infected patients, even in the presence of 'matrix' and other plasma proteins such as albumin and globulin. Even other peptide sequences, similar to epitope sequences only with one or two amino acid mismatches were also unable to show any binding. The analytical performance of DEIP‐EQCM sensor was tested through selectivity, specificity, matrix effect, detection limit (0.68–1.01 nM), quantification limit (2.05–3.05 nM) and reproducibility (RSD ~ 5%). Hence, a diagnostic tool for bacterium causing meningitis is successfully fabricated in a facile manner which will broaden the clinical access and make efficient population screening feasible. [ABSTRACT FROM AUTHOR]

This study focuses on the synthesis, fabrication, and characterization of a molecularly imprinted polymer (MIP) sensor tailored for the selective determination of 4,4′-oxydianiline (4,4′-ODA) in plastic products. Notably, by integrating the sensor matrix with pyrolyzed copper/carbon material derived from Cu-BTC MOF, a remarkable enhancement in electrochemical performance is achieved. The Cu-BTC material is grown successfully on the surface of carbon nanotubes (CNTs) and subjected to calcination at 800 °C, yielding a CNT/Cu/C composite. This composite exhibits an increased surface area and enhanced electron transfer capability, resulting in an improved current response. To augment the selective detection capability of the modified electrodes for 4,4′-ODA, molecularly imprinted polymers (MIPs) were incorporated onto the composite surface. The modified electrode (CNT-2/Cu/C/MIP/GCE) was synthesized using acrylamide (AM) and methacrylic acid (MAA) as dual-functional monomers with 4,4′-ODA as a template molecule via precipitation polymerization. The differential pulse voltammetric (DPV) current response to 4,4′-ODA showed a favorable linear relationship within the concentration range of (0.15–10 μM,10–100 μM), with a detection limit of 0.05 μM. Moreover, the CNT-2/Cu/C/MIP/GCE sensor demonstrates exceptional sensitivity, specificity, consistency, and durability. Furthermore, this approach has proven effective in detecting 4,4′-ODA in spiked nylon spatula samples, with recovery rates ranging from 86.3% to 103.5%. [ABSTRACT FROM AUTHOR]

Introduction: Luteolin (LTL) is the primary active ingredient in honeysuckle, which exhibited wide pharmacological activities, including heat-clearing, detoxifying, anti-inflammatory and anti-oxidant effects. The conventional method for the extraction of LTL consumed a substantial amount of time and organic solvents, and poor selectivity. Therefore, fabrication of novel material with simple preparation process, low cost and excellent selectivity is of great significance for the extraction and enrichment of LTL from honeysuckle. Results: In this system, a novel surface imprinting polymer for luteolin, denoted as Fe3O4@SiO2@MIP, was synthesized using covalent-noncovalent synergistic imprinting strategies. 3-acrylamidephenylboric acid was adopted as covalent functional monomer, deep eutectic solvent (choline chloride/methacrylic acid (ChCl/MAA, 1/2, n/n)) and methacrylic acid as the non-covalent functional monomers, and Fe3O4@SiO2 nanoparticles as the magnetic support. The resultant Fe3O4@SiO2@MIP displayed a uniform morphology, good crystallinity, and excellent magnetic properties. Meanwhile, the binding experiments demonstrated that Fe3O4@SiO2@MIP exhibited high binding performance and the maximum adsorption capacity was 20.97 mg/g. Moreover, the selectivity and reusability behavior of them were satisfactory. In addition, this polymer, serving as an adsorbent, presented practical application potential in separation and enrichment of LTL from honeysuckle. Conclusion: The covalent-noncovalent synergistic imprinting strategy could greatly facilitate the preparation of imprinted nanoparticles for the specific recognition of LTL, providing a valuable approach for the enrichment of LTL in complex samples. [ABSTRACT FROM AUTHOR]

A unique and selective molecularly imprinted polymer (MIP) was fabricated to detect melamine using a quartz crystal microbalance (QCM) surface. The MIP was synthesized by sol–gel technique utilizing 3‐(trimethoxysilyl) propyl methacrylate (TMSPMA) as the functional monomer bearing the methacrylate head group. To identify the melamine, we applied a coating of the as‐synthesized MIP over the silicon crystal of the quartz crystal microbalance (QCM) detector. High‐affinity adsorption of template molecules from the aqueous solution is the basis of the detection. Adsorption experiments performed in real‐time on MIP surfaces indicate that melamine forms strong bonds with its template molecule. We have evaluated the MIP surface using contact angle, BET, RAMAN and AFM investigations regarding wettability, reactivity, surface area, and smoothness. The real‐time adsorption experiments of template molecules on the MIP substrate reveal enhanced attachments with MIP, whereas the NIP demonstrates no interactions with the template molecules. Melamine detection in tainted milk samples further validated the MIP QCM sensor effectiveness. Melamine at a concentration ranging from 1–20 mg/L is tested. Findings conclude that the polymerization method and the QCM nanosensor for selective melamine detection were adequate substitutes for the technologies currently used for detecting melamine. [ABSTRACT FROM AUTHOR]

Stanozolol, a synthetic derivative of testosterone, is one of the common doping drugs among athletes and bodybuilders. It is metabolized to a large extent and metabolites are detected in urine for a longer duration than the parent compound. In this study, a novel dummy molecularly imprinted polymer (DMIP) is developed as a sorbent for solid-phase extraction of stanozolol metabolites from spiked human urine samples. The optimized DMIP is composed of stanozolol as the dummy template, methacrylic acid as the functional monomer, and ethylene glycol dimethacrylate as the cross-linker in a ratio of 1:10:80. The extracted analytes were quantitively determined using a newly developed and validated ultrahigh-performance liquid chromatography tandem mass spectrometry method, where the limits of detection and quantitation were 0.91 and 1.81 ng mL−1, respectively, fulfilling the minimum required performance limit decided on by the World Anti-Doping Agency. The mean percentage extraction recoveries for 3'-hydroxystanozolol, 4β-hydroxystanozolol, and 16β-hydroxystanozolol are 97.80% ± 13.80, 83.16% ± 7.50, and 69.98% ± 2.02, respectively. As such, the developed DMISPE can serve as an efficient cost-effective tool for doping and regulatory agencies for simultaneous clean-up of the stanozolol metabolites prior to their quantification. [ABSTRACT FROM AUTHOR]

Flavonol and flavonoid compounds are important natural compounds with various biomedical activities. Therefore, it is of great significance to develop a strategy for the specific extraction of flavonol and flavonoid compounds. Quercetin is a well-studied flavonoid possessing many health benefits. This compound is a versatile antioxidant known to possess protective abilities against body tissue injury induced by pathological situations and various drug toxicities. Although quercetin is widely distributed in many plants, its content generally is not very high. Therefore, the specific extraction of quercetin as well as other flavonol and flavonoid compounds has profound significance. In this work, the quercetin molecularly imprinting polymer (QMIP) was successfully prepared, in which a typical flavonol quercetin was selected as the template molecule. QMIP was synthesized by performing the surface molecular imprinting technology on the surface of NH2-MIL-101(Fe). Our study results showed that QMIP exhibited quick binding kinetic behavior, a high adsorption capacity (57.04 mg/g), and the specific recognition ability toward quercetin compared with structurally distinct compounds (selective factor > 2). The specific adsorption ability of quercetin by QMIP was further explained using computation simulation that molecules with non-planar 3D conformations hardly entered the molecularly imprinted cavities on QMIP. Finally, QMIP was successfully used for the specific extraction of quercetin and five other flavonol and flavonoid compounds in the crude extracts from Sapium sebiferum. This study proposes a new strategy to synthesize the molecularly imprinted polymer based on a single template for enriching and loading a certain class of active ingredients with similar core structures from variable botanicals. [ABSTRACT FROM AUTHOR]

This study addresses the necessity to monitor the presence of glyphosate (Gly) in waters, highlighting the need for on-site detection of Gly by using electrochemical sensors in environmental and agricultural monitoring programs. Two approaches were employed: (1) modification with graphene decorated with gold nanoparticles (AuNPs-Gr) and dispersed in either dimethylformamide (DMF) or a solution containing Nafion and isopropanol (NAF), and (2) molecularly imprinted polymers (MIPs) based on polypyrrole (PPy) deposited on gold SPEs (AuSPE). Electrochemical characterization revealed that sensors made of AuNPs-Gr/SPCE exhibited enhanced conductivity, larger active area, and improved charge transfer kinetics compared to unmodified SPEs and SPEs modified with graphene alone. However, the indirect detection mechanism of Gly via complex formation with metallic cations in AuNPs-Gr-based sensors introduces complexities and compromises sensitivity and selectivity. In contrast, MIPPy/AuSPE sensors demonstrated superior performance, offering enhanced reliability and sensitivity for Gly analysis. The MIPPy/AuSPE sensor allowed the detection of Gly concentrations as low as 5 ng/L, with excellent selectivity and reproducibility. Moreover, testing in real surface water samples from the Olt River in Romania showed recovery rates ranging from 90% to 99%, highlighting the effectiveness of the detection method. Future perspectives include expanding the investigation to monitor Gly decomposition in aquatic environments over time, providing insights into the decomposition's long-term effects on water quality and ecosystem health, and modifying regulatory measures and agricultural practices for mitigating its impact. This research contributes to the development of robust and reliable electrochemical sensors for on-site monitoring of Glyphosate in environmental and agricultural settings. [ABSTRACT FROM AUTHOR]

Nifedipine (NIF), as one of the dihydropyridine calcium channel blockers, is widely used in the treatment of hypertension. However, misuse or ingestion of NIF can result in serious health issues such as myocardial infarction, arrhythmia, stroke, and even death. It is essential to design a reliable and sensitive detection method to monitor NIF. In this work, an innovative molecularly imprinted polymer dual-emission fluorescent sensor (CDs@PDA-MIPs) strategy was successfully designed for sensitive detection of NIF. The fluorescent intensity of the probe decreased with increasing NIF concentration, showing a satisfactory linear relationship within the range 1.0 × 10−6 M ~ 5.0 × 10−3 M. The LOD of NIF was 9.38 × 10−7 M (S/N = 3) in fluorescence detection. The application of the CDs@PDA-MIPs in actual samples such as urine and Qiangli Dingxuan tablets has been verified, with recovery ranging from 97.8 to 102.8% for NIF. Therefore, the fluorescent probe demonstrates great potential as a sensing system for detecting NIF. [ABSTRACT FROM AUTHOR]

The first electrochemical sensor application in the literature is described for the sensitive and selective determination of the selective Janus kinase (JAK)-1 inhibitor abrocitinib (ABR). ABR is approved by the U.S. Food and Drug Administration (FDA) for the treatment of atopic dermatitis. The molecularly imprinted polymer (MIP)-based sensor was designed to incorporate zinc nanoflower (ZnNFs)-graphene oxide (GO) conjugate (ZnNFs@GO), synthesized from the root methanolic extract (RME) of the species Alkanna cappadocica Boiss. et Bal. to improve the porosity and effective surface area of the glassy carbon electrode (GCE). Furthermore, the MIP structure was prepared using ABR as a template molecule, 4-aminobenzoic acid (4-ABA) as a functional monomer, and other additional components. Scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) were used to characterize the surface and structure of the synthesized nanomaterial and MIP-based surface. Among the electrochemical methods, cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were preferred for detailed electrochemical characterization, and differential pulse voltammetry (DPV) was preferred for all other electrochemical measurements using 5.0 mM [Fe(CN)6]3–/4– solution as the redox probe. The MIP-based sensor, which was the result of a detailed optimization phase, gave a linear response in the 1.0 × 10–13 – 1.0 × 10–12 M range in standard solution and serum sample. The obtained limit of detection (LOD) and limit of quantification (LOQ) values and recovery studies demonstrated the sensitivity, accuracy, and applicability of the sensor. Selectivity, the most important feature of the MIP-based sensor, was verified by imprinting factor calculations using ibrutinib, ruxolitinib, tofacitinib, zonisamide, and acetazolamide. [ABSTRACT FROM AUTHOR]

This work presents an electrochemical sensor detecting a fungicide-azoxystrobin (AZO) in aqueous environments. This AZO sensor utilizes a thin-film metal electrode (TFME) combined with an AZO-selective molecularly imprinted polymer (AZO–MIP). The AZO–MIP was directly generated on TFME through electrochemical polymerization from the solution containing two functional monomers: aniline (Ani) and m-phenylenediamine (mPD), and the template: AZO, which was afterwards removed to form AZO-selective cavities in the polymer matrix. The AZO–MIP preparation was characterized by electrochemical and ellipsometry measurements. Optimization of the synthesis parameters, including the charge density applied during electrodeposition, the monomer-to-template ratio, was performed to enhance the sensor's performance. The results demonstrated that the AZO sensor achieved a low limit of detection (LOD) of 3.6 nM and a limit of quantification (LOQ) of 11.8 nM in tap water, indicating its sensitivity in a complex aqueous environment. The sensor also exhibited satisfactory selectivity for AZO in both ultrapure and tap-water samples and achieved a good recovery (94–119%) for the target analyte. This study highlights the potential of MIP-based electrochemical sensors for the rapid and accurate detection of fungicide contaminants in water, contributing to the advancement of analytical tools for water-quality monitoring and risk assessment. [ABSTRACT FROM AUTHOR]

This experiment addresses the pressing issue of milk safety, integrating cutting-edge molecular imprinting technology into undergraduate laboratory classes. A comprehensive experiment is designed, combining molecular imprinting, protein exclusion, and magnetic separation techniques to synthesize lightweight magnetic molecularly imprinted polymers. The polymers' performance is evaluated, and they are utilized as solid-phase extraction adsorbents in conjunction with high-performance liquid chromatography to establish a novel method for the direct and selective detection of trace tetracycline in milk samples. This interdisciplinary study spans materials chemistry, analytical chemistry, instrumental chemistry, and food chemistry, fostering students' scientific literacy, problem-solving abilities, and innovative thinking. The innovative design of the imprinting material and magnetic separation process ensures cost-effectiveness, ease of operation, and high safety throughout the experiment. Through this hands-on experience, students gain insight into molecular imprinting technology, learn new detection methods, refine basic laboratory skills, enhance data collection and analysis capabilities, and deepen their understanding of the interplay between components, performance, and application. [ABSTRACT FROM AUTHOR]

This study aimed to develop an electrochemical sensor based on a derivative of graphene oxide (GO) and a molecularly imprinted polymer (MIP) on a pencil graphite electrode (PGE) for the detection of ascorbic acid (AA). MIP was fabricated onto the surface of the electrode by electropolymerization technique using cyclic voltammetry with a scan rate of 10 mV/s consisting of template molecule (ascorbic acid), functional monomer (polypyrrole), cross-linker (LiClO4) and citrate buffer at pH 4. Then, the template removal process was conducted to create the imprinted cavities for detecting the analyte. Differential pulse voltammetry (DPV) and cyclic voltammetry (CV) methods were used to perform quantitative analyses of the modified electrodes. CV analysis was performed at the optimum scan rate of 10 mV/s, and the electrolyte concentration at 1.0 mM K3[Fe(CN)6] in 0.1 M KCl. MIP-PGE (2) produced the best performance by having the highest redox peak current response when scanning with the CV compared to other modified electrodes. The optimum parameters for DPV measurement are 100 mV pulse amplitude, 200 ms pulse period, and 10 mV/s scan rate. The straightforward instrumentation and easy preparation of the proposed sensor make it a valuable system for constructing simple devices for determining ascorbic acid. [ABSTRACT FROM AUTHOR]

This study presents the initial attempt at introducing a magnetic molecularly imprinted polymer (MIP) designed specifically for lamotrigine with the purpose of functioning as a drug carrier. First, the composition of the magnetic polymer underwent optimization based on bulk polymer adsorption studies and theoretical analyses. The magnetic MIP was synthesized from itaconic acid and ethylene glycol dimethacrylate exhibiting a drug loading capacity of 3.4 ± 0.9 μg g−1. Structural characterization was performed using powder X-ray diffraction analysis, vibrating sample magnetometry, and Fourier transform infrared spectroscopy. The resulting MIP demonstrated controlled drug released characteristics without a burst effect in the phospahe buffer saline at pH 5 and 8. These findings hold promise for the potential nasal administration of lamotrigine in future applications. [ABSTRACT FROM AUTHOR]

In the global market era, food product control is very challenging. It is impossible to track and control all production and delivery chains not only for regular customers but also for the State Sanitary Inspections. Certified laboratories currently use accurate food safety and quality inspection methods. However, these methods are very laborious and costly. The present review highlights the need to develop fast, robust, and cost-effective analytical assays to determine food contamination. Application of the molecularly imprinted polymers (MIPs) as selective recognition units for chemosensors' fabrication was herein explored. MIPs enable fast and inexpensive electrochemical and optical transduction, significantly improving detectability, sensitivity, and selectivity. MIPs compromise durability of synthetic materials with a high affinity to target analytes and selectivity of molecular recognition. Imprinted molecular cavities, present in MIPs structure, are complementary to the target analyte molecules in terms of size, shape, and location of recognizing sites. They perfectly mimic natural molecular recognition. The present review article critically covers MIPs' applications in selective assays for a wide range of food products. Moreover, numerous potential applications of MIPs in the food industry, including sample pretreatment before analysis, removal of contaminants, or extraction of high-value ingredients, are discussed. [ABSTRACT FROM AUTHOR]

Widely used organophosphorus pesticide triazophos (TAP) can easily cumulate in aquatic system due to its high stability chemically and photochemically and thus posing significant threat to aquatic creatures and humans' health. Urging demand for rapid determining TAP in water has risen. Photoelectrochemical (PEC) sensing turns out to be a good candidate for its simplicity in fabrication and swiftness in detection. Nevertheless, traditional PEC sensors often lack selectivity as their signal generation primarily relies on the oxidation of organic compounds in the electrolyte by photo-induced holes. To address this limitation, molecularly imprinted polymers (MIPs) can be in combined with PEC sensors to significantly enhance the selectivity. Here, we present a novel approach utilizing a PEC sensor enhanced by carbon-modified titanium dioxide molecularly imprinted polymers (MIP/C/TiO2 NTs). Carbon quantum dot (CQD) modification of titanium dioxide nanotube arrays (C/TiO2 NTs) was achieved through a one-step anodization process, effectively enhancing visible light absorption by narrowing the band gap of TiO2, and CQDs also function as sensitizer accelerating charge transfer for improved and stable photocurrent signals during detection. Our method further incorporates MIPs to heighten the selectivity of the PEC sensor. Electro-polymerization using cyclic voltammetry was employed to polymerize MIPs with pyrrole as the functional monomer and triazophos as the target molecule. The resultant MIP/C/TiO2 NT sensor exhibited remarkable sensitivity, with a detection limit of 0.03 nM (S/N = 3), alongside exceptional selectivity and stability for triazophos detection in water. This offers a promising avenue for efficient, cost-effective, and rapid monitoring of pesticide contaminants in aquatic environments, contributing to the broader goals of environmental preservation and public health. [ABSTRACT FROM AUTHOR]

A comparative analysis of molecularly imprinted polymers based on different synthesis techniques was performed for the recognition of molnupiravir (MOL). The polymerizations were performed with 3-thienyl boronic acid (3-TBA) as a functional monomer by electropolymerization (EP) and with guanine methacrylate (GuaM) as a functional monomer by photopolymerization (PP). Morphological and electrochemical characterizations of the developed sensors were investigated to verify the constructed sensors. Moreover, quantum chemical calculations were used to evaluate changes on the electrode surface at the molecular and electronic levels. The dynamic linear range of both designed sensors under optimized experimental conditions was found to be 7.5 × 10−12–2.5 × 10−10 M and 7.5 × 10−13–2.5 × 10−11 M for EP and PP, respectively. The effect of various interfering agents on MOL peak current was assessed for the selectivity of the study. In the presence of 100 times more interfering agents, the RSD and recovery values were determined. The RSD values of GuaM/MOL@MIP/GCE and poly(Py-co-3-PBA)/MOL@MIP/GCE sensors were found to be 1.99% and 1.72%, respectively. Furthermore, the recovery values of the MIP-based sensors were 98.18–102.69% and 98.05–103.72%, respectively. In addition, the relative selectivity coefficient (k′) of the proposed sensor was evaluated, and it exhibited good selectivity for MOL with respect to the NIP sensor. The prepared sensor was successfully applied to determine MOL in commercial serum samples and capsule form. In conclusion, the developed sensors provided excellent reproducibility, repeatability, high sensitivity, and selectivity against the MOL molecule. [ABSTRACT FROM AUTHOR]

Alumina inorganic molecularly imprinted polymer (MIP) modified multi-walled carbon nanotubes (MWCNTs) on a glassy carbon electrode (MWCNTs-Al2O3-MIP/GCE) was firstly designed and fabricated by one-step electro deposition technique for the detection of uric acid (UA) in sweat. The UA templates were embedded within the inorganic MIP by co-deposition with Al2O3. Through the evaluation of morphology and structure by Field Emission Scanning Electron Microscope (SEM), Energy Dispersive X-ray Spectroscopy (EDS), X-ray Photoelectron Spectroscopy (XPS) and Transmission Electron Microscopy (TEM), it was verified that the specific recognition sites can be fabricated in the electrodeposited Al2O3 molecular imprinted layer. Due to the high selectivity of molecular imprinting holes, the MWCNTs-Al2O3-MIP/GCE electrode demonstrated an impressive imprinting factor of approximately 2.338 compared to the non-molecularly imprinted glassy carbon electrode (MWCNTs-Al2O3-NIP/GCE) toward uric acid detection. Moreover, it exhibited a remarkable limit of detection (LOD) of 50 nM for UA with wide detection range from 50 nM to 600 μM. The MWCNTs-Al2O3-MIP/GCE electrode also showed strong interference resistance against common substances found in sweat. These results highlight the excellent interference resistance and selectivity of MWCNTs-Al2O3-MIP/GCE sensor, positioning it as a novel sensing platform for non-invasive uric acid detection in human sweat. [ABSTRACT FROM AUTHOR]

High cholesterol grades are a significant threat factor for coronary heart disease, which leads to heart attacks. General practices focus on lowering cholesterol and saturated fatty acids in the diet to decrease the incidence of cardiovascular diseases. Milk is a primary food with high nutritional value and high consumption. Molecularly imprinted cryogels are an excellent alternative according to non-selective methods such as liquid–liquid and/or solid-phase extraction to elute cholesterol selectively from milk. Because the cryogels are low cost, they can be synthesized easily, and the sample can be applied directly to the cryogel without needing any pre-treatment. In this study, we synthesized cholesterol-imprinted (Chl-MIP) cryogel membranes employing aminoacid-based hydrophobic functional comonomer N-methacryloyl-L-phenylalanine to be used as a selective adsorbent to remove cholesterol from milk samples. Chl-MIP cryogel exhibited a maximum Chl adsorption capacity of 12.01 mg/g at 25 °C with an interaction time of 60 min. The selectivity of the cryogel was 2.89 times greater for estradiol molecules and 4.99 times greater for progesterone molecules. Chl-MIP cryogel provides a rapid mass transfer by a short diffusion path without any diffusion restrictions. This process is simple to implement, efficient, affordable, and feasible for use on modern manufacturing lines. [ABSTRACT FROM AUTHOR]

In this study, a novel magnetic molecularly imprinted polymeric material (Fe3O4@MOF@MIP-160) with a metal-organic backbone (Fe3O4@MOF) carrier was prepared using dibutyl phthalate (DBP) as a template. The material can be used for the efficient, rapid, and selective extraction of trace amounts of phthalic acid esters (PAEs) in food and can detect them via gas chromatography-mass spectrometry (GC-MS). The synthesis conditions of the materials were optimized to prepare the Fe3O4@MOF@MIP160 with the highest adsorption performance. Transmission electron microscopy (TEM), Fourier Transform Infrared Spectra (FT-IR), Vibration Sample Magnetic (VSM), and the Brunauer–Emmett–Teller (BET) method were used to characterize the materials. Compared with Fe3O4@MOF and the magnetic non-imprinted polymeric material (Fe3O4@MOF@NIP), Fe3O4@MOF@MIP-160 possesses the advantages of easy and rapid manipulation of magnetic materials, the advantages of high specific surface area and the stability of metal–organic frameworks, and the advantages of high selectivity of molecularly imprinted polymers. Fe3O4@MOF@MIP-160 has good recognition and adsorption capacity for di-butyl phthalate (DBP) and diethylhexyl phthalate (DEHP): the adsorption capacity for DBP and DEHP is 260 mg·g−1 and 240.2 mg·g−1, and the adsorption rate is fast (reaching equilibrium in about 20 min). Additionally, Fe3O4@MOF@MIP160 could be recycled six times, making it cost-effective, easy to operate, and time-saving as compared to traditional solid-phase extraction materials. The phthalate ester content in drinking water, fruit juice, and white wine was analyzed, with recoveries ranging from 70.3% to 100.7%. This proved that Fe3O4@MOF@MIP160 was suitable for detecting and removing PAEs from food matrices. [ABSTRACT FROM AUTHOR]

In this study, a novel methodology has been developed for the rapid and sensitive analysis of bongkrekic acid (BA), a highly toxic bacterial metabolite, using a molecularly imprinted polymer-coated wooden-tip coupled with electrospray ionization mass spectrometry (MIPWT-ESI-MS). A MIPWT solid phase microextraction (SPME) probe specifically tailored for BA was fabricated, by employing dummy template molecules/functional monomers in the imprinting coating modification. This approach exhibits an enrichment factor (EF) of 683 ± 53 for efficient extraction of BA from aqueous matrices, demonstrating the utility of dummy templates in enhancing the selectivity and sensitivity of the MIPWT-ESI-MS method. The analytical performance of the MIPWT-ESI-MS method was evaluated, demonstrating a desirable linear correlation (r = 0.9988), along with remarkable sensitivity by a limit of detection (LOD) and limit of quantitation (LOQ) at 0.05 μg/L and 0.16 μg/L in pure water, respectively. Additionally, the method demonstrated high repeatability with a relative standard deviation (RSD) < 3.9 % (n = 6) and reproducibility with an RSD < 13.4 %. The practical application of the method was confirmed through the successful analysis of real-world samples, including tap water, wastewater from a food processing factory, and the aqueous extracts of food samples, with BA detected at 0.296 µg/L in Tremella. Spiking experiments further validated the accuracy of the method, with recoveries ranging from 81 % to 97 %. This study integrates MIP with ambient mass spectrometry, offering a robust, selective, and sensitive tool for the monitoring of trace BA levels in complex food and environmental samples, contributing significantly to public health safety and food quality control.

Cardiovascular disease (CVD) is the leading cause of mortality around the world. Diagnosis of CVD using biosensing strategy poised to improve the precision and efficiency of CVD treatment in standard clinical practice. Electrochemical biosensors show great promise for early and accurate diagnosis of cardiovascular diseases, paving the way for personalized medicine and improved patient outcomes. Nanomaterials are emerging as a must need tool in biosensor fabrication. Graphene-based nanomaterials exhibit exceptional electrical conductivity, large surface area, and enhanced biofunctionalization ability for the receptor molecules, serving as an ideal platform for sensitive and selective biosensing applications, which in turn offers high sensitivity, rapid response times, and portability, making them ideal for point-of-care testing. The use of aptamers or molecularly imprinted polymers over antibodies as receptor can provide tool to develop innovative, highly stable biosensors over classical biosensors. In this review, electrochemical state-of-art technology for biosensor development incorporating graphene-related nanomaterials are discussed. Recently developed graphene-based electrochemical nanobiosensors for cardiac biomarker detection are reviewed. Current trends in biosensing strategy and future perspectives are outlined, with a focus on the potential use of graphene-related nanomaterials in electrochemical biosensing platforms.

In this work, the authors represent a comprehensive approach for the development and validation of a novel graphite-supported molecularly imprinted poly(methyl methacrylate) electrode for the selective and sensitive detection of aloe emodin (AE) in aloe-based cosmetic products. The electrocatalytic activity of the electrode was evaluated using cyclic voltammetry and differential pulse voltammetry techniques in phosphate buffer saline. Surface morphology, structural characteristics, and imprinting endorsement were investigated using field emission scanning electron microscopy, Fourier-transform infrared spectroscopy, and UV-Vis spectroscopy. Under the optimal conditions, the electrode showed an oxidative differential pulse voltammetry peak at -0.2931±0.011 V (vs. Ag/AgCl, saturated KCl). The current was increased linearly with increasing concentrations of AE from 0.0005 to 350 µM, with a low detection limit of 0.0003 µM. The voltammetric analysis has been validated by reverse-phase high-performance liquid chromatography (RP-HPLC) methods. A partial least square regression model was developed to correlate the results obtained from the proposed system with the reference values obtained by RP-HPLC. The model showed a high prediction accuracy of 95.95 % for the detection of AE in cosmetic samples. The developed electrode provides a low-cost, rapid, easy, and convenient method for the detection of AE in cosmetic products, offering potential benefits for quality control and safety assessment in the cosmetic industry.

Abstract The antiretroviral drugs (ARVDs) have been reported to be among the emerging water pollutants as a results attention is being paid on their analysis. This work therefore explored for the first time the multi-template MIP for the selective removal of selected ARVDs (abacavir, efavirenz and nevirapine) in wastewater, river water and tap water. The adsorption studies of a multi-template MIP were conducted by determining the effect of an increase in ARVDs concentration in solution and the effect of an increase in contact time between the sorbent and the ARVDs. High adsorption efficiencies were observed for abacavir, efavirenz and nevirapine analytes within 5 min and the maximum adsorption efficiency was observed at 60 min ranging from 94.76 to 96.93%. Adsorption kinetics showed that pseudo-second rate order was the best fitting model, while adsorption isotherms indicated that the Freundlich isotherm (R 2 = 0.94–0.98) best described the adsorption mechanism of ARVDs onto the MIPs. These results indicated that the electrostatic attractions influenced the multilayer coverage and chemisorption process. Selectivity studies conducted in the presence of competitors gave the recoveries between 92 and 98% for the target analytes, while they were 63–79% for competitors indicating good selectivity and strong affinity of the polymer towards the target analytes. Reusability studies showed that the MIP can be reused for up to 8 cycles with recoveries above 92% for all target ARVDs. The application of the MIP-DSPE method to wastewater, river and tap water samples gave concentrations of 28.75–178.02, 1.95–13.15 and 2.17–6.27 µg L−1, respectively. These results indicate the potential unplanned consumption of ARVDs upon drinking contaminated water which could result to their resistance by the human body. Therefore, their continuous monitoring as well as investigation of their removal strategies is of paramount importance.

Abstract Glyphosate (GLY) is a widely used herbicide with an important role in agriculture. It effectively controls weeds, enhancing agricultural yield and product quality. However, its use raises significant concerns such as potential risks to non-target ecosystems and human health. In response to these concerns, we develop an electrochemical sensor with a molecularly imprinted polymer (MIP) and gold nanoparticles for GLY detection. The sensor includes a screen-printed carbon electrode (SPCE) functionalized with gold nanoparticles and a self-assembled polyvinyl carboxylic acid chloride (PVC-COOH) layer. GLY compounds interact with carboxylic groups and are encapsulated by a polymer of methacrylic acid (MAA) cross-linked with ethylene glycol dimethacrylate (EGDMA). Electrochemical performance was assessed using differential pulse voltammetry (DPV), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). Morphological characterization was performed using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and atomic force microscopy (AFM). The sensor exhibits impressive selectivity, detecting GLY within a range of 273–1200 pg/mL with minimal interference from other pesticides. It boasts a low detection limit of 0.8 pg/mL (signal-to-noise ratio S/N = 3) by DPV and 0.001 pg/mL by EIS. The sensor’s versatility extends to various sample types, including surface water, agricultural wastewater, soil, and cucumber, demonstrating high recovery rates (> 96.05%) and low relative standard deviation (RSD) (