The authors report on a surface molecular imprinting strategy for synthesizing magnetic and molecularly imprinted core-shell polymer nanoparticles (MMIPs) with a typical size of 320 nm. The triazophos-imprinted polymer shell on 180-nm magnetite particles (modified with 3-methacryloxypropyl trimethoxysilane) was obtained by radical polymerization of ethylene glycol dimethacrylate in the presence of triazophos, this followed by extractive removal of triazophos. The resulting MMIPs possess large binding capacity, high recognition selectivity, and fast binding kinetics for triazophos. They can be easily separated from a solution by using a magnet. These features result in a convenient and selective solid-phase extraction procedure for triazophos prior to its determination by UV spectrometry or by GC analysis. The method was successfully applied to the extraction and clean-up of triazophos residues in spiked homogenates of vegetables with recoveries in the range of 89.2 ~ 99.0%. The detection limits for triazophos by the UV assay and GC assay are 0.93 nM and 0.32 nM, respectively.
Graphical abstract The core-shell magnetic molecularly imprinted polymer nanoparticles (MMIPs) with a nanoscale triazophos-imprinted polymer shell were prepared by surface imprinting onto the surfaces of 3-methacryloxypropyl trimethoxysilane (MATS) modified Fe3O4 magnetic nanoparticles. They were successfully applied for the extraction and clean-up of ultra trace triazophos residues in spiked homogenates of vegetable samples. MMIPs exhibit the larger binding capacity, faster binding kinetics, higher recognition selectivity, good reusability and stability, and excellent magnetic responses.
A magnetic nanosorbent was prepared from Fe3O4 nanoparticles and polyacrylamide using a solvothermal process. Two functions are achieved simultaneously in this process: The first consists in the formation of a carbon layer around the Fe3O4 nanoparticles, and the second one in the functionalization with an amido group. This combination allows the protection of Fe3O4 nanoparticles from dissolution in acid medium during heavy metal adsorption. The adsorbent was characterized by SEM, TEM, EDS, FTIR, TGA, and in terms of surface area. Results showed the Fe3O4 nanoparticles to be embedded in a sheet of carbon with folded surfaces which is functionalized with amido groups. The nanosorbent was applied to the enrichment of Cr(III), Co(II), Cd(II), Zn(II) and Pb(II) via magnetic solid phase extraction (mag-SPE). The effects of pH value, eluent type and sample volume were optimized. The validation of the procedure was verified by the analysis of a wheat gluten certified reference material (8418). The limits of detection for the above ions range from 1 to 110 ng L?1. The relative standard deviations are <10%. The procedure was successfully applied to the enrichment of Cr(III), Co(II), Cd(II), Zn(II) and Pb(II) from various water and food samples.
Graphical abstract Schematic of a new magnetic nanosorbent synthesized from Fe3O4 nanoparticles and polyacrylamide using a solvothermal method. The sorbent was used for the enrichment of Cr(III), Co(II), Cd(II), Zn(II) and Pb(II) in water and food samples for their ICP-MS detection.
A magnetic glassy carbon electrode (mGCE) was modified with a ternary composite prepared from Prussian blue (PB), magnetite (Fe3O4) nanoparticles, and reduced graphene oxide (rGO) in order to obtain an amperometric sensor for hydrazine. The utilization of Fe3O4 facilitates the magnetic immobilization and separation of sensing material, while the use of rGO enhances sensitivity. The surface coverage and the stability of the PB on the modified electrode were considerably improved. The electro-oxidative response to hydrazine was investigated with this modified mGCE using cyclic voltammetry and amperometric. The sensor, typically operated at a voltage of 0.2 V (vs. SCE), displays superior response hydrazine, with a response time of 4 s, a sensitivity of 97.73 μA μM?1 cm?2 and a 13.7 nM detection limit.
Graphical abstract A magnetic glassy carbon electrode was modified with a ternary composite prepared from Prussian blue, magnetite nanoparticles, and reduced graphene oxide to obtain a selective amperometric sensor for dissolved hydrazine.
An ion imprinted polymer coated onto magnetite (Fe3O4) nanoparticles is shown to be a useful magnetic sorbent for the fairly selective preconcentration of vanadium. The sorbent was prepared by radical copolymerization of 3-(triethoxysilyl)propyl methacrylate (the monomer), ethylene glycol dimethacrylate (the cross-linker), and the vanadium(IV) complex of 1-(2-pyridylazo-2-naphthol) in the presence of magnetite nanoparticles. The material was characterized by IR spectroscopy, scanning electron microscopy, and thermal analysis. The vanadium(IV) ions were removed from the imprint by a solution containing thiourea and HCl, and the eluent was submitted to AAS. The analytical efficiency and relative standard deviation are 99.4 and ±2.3 %, respectively, under optimum conditions, and the limit of detection is 20 ng mL−1. The method was successfully applied to the preconcentration and determination of vanadium(IV) ions in crude oil.
An ion imprinted polymer is coated on to magnetite nanoparticles as a useful magnetic sorbent for the fairly selective preconcentration of vanadium which can be used for vanadium determination in crude oil.
We describe a colorimetric assay for mercury(II) ion. It is based on a hybridization chain reaction (HCR) and the use of Fe3O4@Au nanoparticles (NPs). Aptamers specific for Hg(II) were immobilized on the surface of the Fe3O4@AuNPs. The presence of Hg(II) inhibits the HCR process and this enables less Methylene Blue (MB) to intercalate into the dsDNA structure. After magnetic separation of the DNA-loaded NPs carrying Hg(II), the change in the absorbance of the residual MB solution is measured at 663 nm. The respective calibration plot is linear in the 1 to 300 nM concentration range, with a 0.7 nM detection limit (at a signal-to-noise ratio of 3). The method displays excellent selectivity over other metal ions. It was applied to the analysis of Hg(II) in spiked river water.
Graphical abstract Fe3O4@Au nanoparticles (NPs) were fabricated, then aptamers were modified on the surface of Fe3O4@AuNPs. The absence of Hg2+ leads to the formation of dsDNA polymers via hybridization chain reaction (HCR) process on the surface of Fe3O4@AuNPs, Methylene Blue (MB) intercalates into these DNA polymers, which can be easily separated from MB solution by applying a magnet, thereby inducing a color change of the MB solution.
The authors describe an aptamer-based fluorescent assay for adenosine (Ade). It is based on the interaction between silver nanoparticles (AgNPs) and CdTe quantum dots (QDs). The beacon comprises a pair of aptamers, one conjugated to Fe3O4 magnetic nanoparticles, the other to AgNPs. In the presence of Ade, structural folding and sandwich association of the two attachments takes place. After magnetic separation, the associated sandwich structures are exposed to the QDs. The AgNPs in sandwich structures act as the signaling label of Ade by quenching the fluorescence of QDs (at excitation/emission wavelengths of 370/565 nm) via inner filter effect, electron transfer and trapping processes. As a result, the fluorescence of QDs drops with increasing Ade concentration. The assay has a linear response in the 0.1 nM to 30 nM Ade concentration range and a 60 pM limit of detection. The assay only takes 40 min which is the shortest among the aptamer-based methods ever reported. The method was successfully applied to the detection of Ade in spiked biological samples and satisfactory recoveries were obtained.
Graphical abstract Schematic of a highly efficient and convenient adenosine (Ade) fluorometric assay. It is based on the interaction between Ag nanoparticles (NPs) and CdTe quantum dots (QDs). Ade aptamers (ABA1 and ABA2) are used as recognition unit and Fe3O4 magnetic nanoparticles act as magnetic separator. The assay exhibits superior sensitivity and speediness.
An electrochemical quercetin (QR) sensor is described that is based on the use of magnetic reduced graphene oxide (MrGO) incorporated into a molecularly imprinted polymer (MIP) on the surface of a screen-printed electrode (SPE). The MrGO consists of reduced graphene oxide (rGO), magnetite (Fe3O4) and silver nanoparticles (Ag). The analyte (QR) is electrostatically adsorbed on the surface of the MrGO. Finally, the MIP was deposited via in-situ polymerization. The composite was characterized by X-ray diffraction, Fourier transform infrared spectroscopy and Vibrating sample magnetometry. The morphologies and electrochemical properties of different electrodes were characterized by Field emission scanning electron microscopy, Electrochemical impedance spectroscopy and differential pulse voltammetry. Under optimal conditions, the modified electrode has a linear response in the 20 nM to 250 μM QR concentration range. The limit of detection is 13 nM (at an S/N ratio of 3). The electrode is selective, stable, regenerable and reliable. It was applied to the determination of QR in spiked pharmaceutical samples and gave satisfactory results.
Graphical abstract Schematic presentation of a method for sensing quercetin. It is based on the use of screen printed electrode modified with magnetized reduced graphene oxide and a molecularly imprinted polymer.
An electrochemical microsensor for chloramphenicol (CAP) was fabricated by introducing magnetic Fe3O4 nanoparticles (NPs) onto the surface of activated carbon fibers. This microsensor exhibited increased electrochemical response toward CAP because of the synergetic effect of the Fe3O4 NPs and the carbon fibers. Cyclic voltammograms were acquired and displayed three stable and irreversible redox peaks in pH 7.0 solution. Under optimized conditions, the cathodic current peaks at ?0.67 V (vs. Ag/AgCl). The calibration plot is linear in the 40 pM to 1 μM CAP concentration range, with a 17 pM detection limit (at a signal-to-noise ratio of 3). The sensor was applied to the determination of CAP in spiked sediment samples. In our perception, this electrocatalytic platform provided a useful tool for fast, portable, and sensitive analysis of chloramphenicol.
Graphical abstract A sensitive carbon fiber microsensor modified with Fe3O4 nanoparticles is found to display two cathodic peaks when detecting chloramphenicol at 100 mV·s?1 and at pH 7.0. The sensor was applied to the determination of chloramphenicol in sediment samples.
This review (with 144 refs.) focuses on the recent advances in the preparation and application of magnetic micro/nanoparticles. Specifically, it covers (a) methods for preparation (such as by coprecipitation, pyrolysis, hydrothermal, solvothermal, sol-gel, micro-emulsion, sonochemical, medium dispersing or emulsion polymerization methods), and (b) applications such as magnetic resonance imaging, magnetic separation of biomolecules (nucleic acids; proteins; cells), separation of metal ions and organic analytes, immobilization of enzymes, biological detection, magnetic catalysis and water treatment. Finally, the existing challenges and possible trends in the field are addressed.
Graphical abstract This review focuses on the recent advances in the preparation and application of magnetic micro/nano particles. Finally, the existed problems and possible trends in the field were discussed. a: Fe3O4@SiO2-PVAm: polyvinyl amine-coated Fe3O4@SiO2 b: CTS/MMT-Fe3O4 microsphere: chitosan/montmorillonite-Fe3O4 microsphere c: MTAMs: magnetic targeted antibiotic microspheres d: SM: the code of iron oxide-silica composite microspheres e: PSt: poly styrene f: gamma-PGA- PLA: poly(gamma-glutamic acid) and poly(lactide) g: poly(-MMA–DVB–GMA) microspheres: poly(methylmethacrylate–divinylbenzene–glycidylmethacrylate) microspheres h: AEAPS: N-(2-aminoethyl)-3-aminopropyltrimethoxysilane
Photonic encoding magnetized silica microspheres were synthesized from a polydisperse system containing silica and Fe3O4 nanoparticles by using a microfluidic self-assembly device. The optical and structural properties of the magnetized microspheres were characterized by scanning electron microscopy and reflection spectra. The concentration of Fe3O4 nanoparticles in polydisperse system was found to strongly affect the characteristics of magnetized microspheres. They possess a Janus face, are porous, and possess structural color (red). The magnetic characteristic of the synthesized microspheres is not lost after they are immersed in piranha solution for 12 h. The magnetized microspheres were applied to aptamer-based enrichment of the food toxin Ochratoxin A (OTA). Methods for immobilization of OTA aptamer on the microsphere surfaces were investigated. The modified microspheres can extract up to 80% of OTA if the surface of the microspheres is loaded with 275 ng·cm?2 of aptamer and the number of microspheres is 200. The work provides a new pathway for aptamer-based enrichment of small molecules from complex matrixes.
Graphical abstract Photonically encoded magnetized silica microspheres were synthesized by using microfluidic self-assembly device. The optical, magnetic and structural properties of the microspheres were investigated. The three-dimensional porous magnetized microspheres were applied to aptamer-based enrichment of the food toxin Ochratoxin A.
The article describes the synthesis of core-shell magnetic nanoparticles (MNPs) of the type Fe3O4@MIL-100 (MIL standing for Material Institut Lavoisier), and their application as sorbent for magnetic solid-phase extraction (MSPE) of triclosan. The MNPs were prepared via circular self-assembly of ferric chloride and benzenetricarboxylic acid. The functionalized MNPs were characterized by transmission electron microscopy, FTIR and thermogravimetry. Following extraction, triclosan was eluted with ammoniacal methanol and then submitted to HPLC with UV detection. The amount of magnetic microspheres, sample pH and ionic strength, adsorption time, desorption time, desorption solvent and the volume of the eluent were optimized. Under optimum conditions, the method showed good linearity in the 0.1 to 50 mg·kg?1 triclosan concentration range in toothpaste samples. Other features include (a) intra-day and inter-day relative standard deviations (RSD, for n = 4) of <5.5 %, (b) a 30 μg·kg?1 limit of detection, and (c) extraction recoveries between 90.86 % and 101.1 %. The method was successfully applied to the determination of triclosan in children’s toothpaste.
Graphical abstract The article describes the synthesis of core-shell magnetic nanoparticles (MNPs) of the type Fe3O4@MIL-100, and their application as sorbent for magnetic solid-phase extraction (MSPE) of triclosan.
A polydopamine-based molecularly imprinted polymer was deposited on the surface of magnetite (ferroferric oxide) nanoparticles (Fe3O4@PDA MIPs) and is shown to be an efficient and fairly specific sorbent for the extraction of various ochratoxins. The MIPs were characterized by IR spectroscopy and transmission electron microscopy. The adsorption capacities, evaluated through the langmuir adsorption isotherm model, are 1.8, 0.23 and 0.17 mg·g?1 for ochratoxin A, ochratoxin B and ochratoxin C, respectively. Parameters such as the amount of magnetic MIPs, pH value, time for ultrasonication, elution solvent and volume were optimized. Following desorption from the MIP with acetonitrile, the ochratoxins were quantified by HPLC with fluorometric detection. Under optimal experimental conditions, the calibration plots are linear in the range of 0.01–1.0 ng·mL?1 of OTA, 0.02–2.0 ng·mL?1 of OTB, and 0.002–0.2 ng·mL?1 of OTC. The LODs are between 1.8 and 18 pg·mL?1, and the recoveries from spiked samples are 71.0% - 88.5%, with RSDs of 2.3–3.8% in case of rice and wine samples. The MIPs can be re-used for at least 7 times.
Graphical abstract Schematic of the preparation of a magnetic molecularly imprinted polymer based on self-polymerization of dopamine in weakly alkaline solution. Ochratoxins are recognized owing to homologous cavities in the MIPs, and quantified by HPLC after desorption with acetonitrile.
A multifunctional fluorescent probe is synthesized for the determination of adenosine 5′-triphosphate (ATP). The 6-carboxyfluorescein-labeled aptamer (FAM-aptamer) was bound to the surface of magnetite nanoparticles coated with polydopamine (Fe3O4@PDA) by π-π stacking interaction to form the multifunctional probe. The probe has three functions including recognition, magnetic separation, and yielding a fluorescent signal. In the presence of ATP, FAM-aptamer on the surface of the probe binds to ATP and returns to the solution. Thus, the fluorescence of the supernatant is enhanced and can be related to the concentration of ATP. Fluorescence intensities were measured at excitation/emission wavelengths of 494/526 nm. Response is linear in the 0.1–100 μM ATP concentration range, and the detection limit is 89 nM. The probe was applied to the quantitation of ATP in spiked human urine and serum samples, with recoveries ranging between 94.8 and 102%.
Graphical abstract A multifunctional fluorescent probe based on the use of FAM-aptamer and Fe3O4@PDA is described for the determination of ATP in spiked human urine and serum samples. FAM-aptamer: 6-carboxyfluorescein-labeled aptamer; Fe3O4@PDA: magnetite nanoparticles coated with polydopamine. ATP: adenosine 5′-triphosphate.
The author describes the preparation of a magnetic metal organic framework of type MOF-199 containing magnetite (Fe3O4) nanoparticles carrying covalently immobilized 4-(thiazolylazo) resorcinol (Fe3O4@TAR). This material is shown to represent a viable sorbent for separation and preconcentration of Cd(II), Pb(II), and Ni(II) ions. Box-Behnken design was applied to optimize the parameters affecting preconcentration. Following elution with 0.6 mol L?1 EDTA, the ions were quantified by FAAS. The capacity of the sorbent ranged between 185 and 210 mg g?1. The limits of detection are 0.15, 0.40, and 0.8 ng mL?1 for Cd(II), Ni(II), and Pb(II) ions, respectively. The relative standard deviations are <8.5 %. The method was successfully applied to the rapid extraction of trace amounts of these ions from sea food and agri food.
Graphical abstract (a) A schematic diagram of Fe3O4 functionalization by TAR (4-(thiazolylazo) resorcinol). (b) The schematic illustration of the magnetic metal organic framework-TAR nanocomposite. H3BTC: benzene-1,3,5-tricarboxylic acid; TEA: triethylamine; 3-CPS: 3-chloropropyl triethoxysilane.
Magnetic microspheres (Fe3O4) were coated with polydopamine (PDA) and loaded with the metal ions Ti(IV) and Nb(V) to give a material of type Fe3O4@PDA-Ti/Nb. It is shown to be useful for affinity chromatography and for enrichment of phosphopeptides from both standard protein solutions and real samples. For comparison, such microspheres loaded with single metal ions only (Fe3O4@PDA-Ti and Fe3O4@PDA-Nb) and their physical mixtures were also investigated under identical conditions. The binary metal ion-loaded magnetic microspheres display better enrichment efficiency than the single metal ion-loaded microspheres and their physical mixture. Both multiphosphopeptides and monophosphopeptides can be extracted. The Fe3O4@PDA-Ti/Nb microspheres exhibit ultra-high sensitivity (the lowest detection amount being 2 fmol) and selectivity at a low mass ratio such as in case of β-casein/BSA (1:1000).
Graphical abstract Magnetic microspheres (Fe3O4) were coated with polydopamine (PDA) and loaded with the metal ions Ti(IV) and Nb(V) to give a material of type Fe3O4@PDA-Ti/Nb. Results showed its great potential as an affinity probe in phosphoproteome research due to rapid magnetic separation of phosphopeptides, ultrahigh sensitivity and selectivity, and remarkable reusability.
Magnetic knitting aromatic polymers (Fe3O4/KAPs) are introduced here as a new kind of sorbents. KAPs are hyper-cross-linked-polymers that were prepared via a Friedl-Crafts reaction from triphenylphosphine and benzene as building blocks. The Fe3O4/KAP composite was obtained by coprecipitation of KAP with magnetite nanoparticles. The resulting Fe3O4/KAP is shown to be a viable magnetic sorbent for various organic materials such as the phenylurea herbicides (PUHs), including metoxuron, monuron, chlortoluron, monolinuron and buturon, and also for various phthalates, polycyclic aromatic hydrocarbons and chlorophenols. The Fe3O4/KAP was characterized by means of Brunauer-Emmett-Teller surface area measurements, Fourier-transform infrared spectroscopy, thermogravimetry, X-ray diffraction, scanning electron microscopy and transmission electron microscopy. Following desorption with acetonitrile, the analytes were quantified by using HPLC with UV detection. The effects of adsorbent dosage, extraction time, sample pH, ionic strength, desorption solvent and desorption time were optimized for the PUHs. Under optimal conditions, response is linear from 0.5–1.0 up to 50 ng·mL?1 for the five PUHs. Lower limits of detection range between 0.05 and 0.30 ng·mL?1. Other figures of merit include (a) high enrichment factors (60–297), (b) good recoveries (91.8–106.5%), and (c) relative standard deviations of <8.4%. The method was successfully applied to analysis of the PUHs in real samples (bottled mixed juice, milk and soymilk). The results indicate that such Fe3O4/KAPs have a wide application scope as an adsorbent for use in magnetic solid phase extraction.
Graphical abstract A magnetic knitting aromatic polymer based nanocomposite (Fe3O4/KAP) was prepared by a one-pot method and explored as an absorbent for magnetic solid-phase extraction (MSPE) of phenylurea herbicides (PUHs) from bottled mixed juice, milk and soymilk samples before quantitation by HPLC with UV detection.
Magnetite nanoparticles were surface-modified with mercaptoacetic acid (MAA), complexed with Zn(II), and then treated with the dual Schiff base (referred to as imine-based ligand; IBL; obtained by reaction of p-aminobenzoic acid and 2,3-butanedione) to give particles with an architecture of type Fe3O4@MAA@IBL. These are shown to be viable sorbents for magnetic solid phase extraction of organochlorine pesticides (OCPs) from seawater samples. Efficient extraction of the OCPs probably is due to lone pair-π, π-complexation and π-interactions. The sorbent was characterized by transmission electron microscopy, scanning electron microscopy, FT-IR and energy-dispersive X-ray spectroscopy. The effects of the volumes of sample, sorbent dosage and eluent, adsorption and desorption times, and the salinity of the sample on the extraction efficiencies were optimized. The OCPs (heptachlor, aldrin, dieldrin, p,p’-DDE and p,p’-DDT) were quantified by gas chromatography with microelectron capture detection. Under optimal conditions, the limit of detections range was between 1.0 and 1.9 ng L?1. The enrichment factors are between 84.1 and 99.9 %. The sorbent was applied to the rapid extraction of trace quantities of OCPs from seawater samples and gave good relative recoveries (78 to 108 %) and relative standard deviations (<8.3 %).
Graphical Abstract Fe3O4 nanoparticles were functionalized with mercaptoacetic acid. The carboxylate was coordinated with Zn(II) and the ligands were immobilized via coordination with Zn(II). The lone pair-π, π-complexation and π-interaction of modified magnetite nanoparticles made this sorbent effective for extraction of organochlorine pesticides.
We are presenting magnetic molecularly imprinted polymer nanoparticles (m-MIPs) for solid-phase extraction and sample clean-up of paracetamol. The m-MIPs were prepared from magnetite (Fe3O4) as the magnetic component, paracetamol as the template, methacrylic acid as a functional monomer, and 2-(methacrylamido) ethyl methacrylate as a cross-linker. The m-MIPs were then characterized by transmission electron microscopy, FT-IR spectroscopy, X-ray diffraction and vibrating sample magnetometry. The m-MIPs were applied to the extraction of paracetamol from human blood plasma samples. Following its elution from the column loaded with the m-MIPs with an acetonitrile-buffer (9:1) mixture, it was submitted to HPLC analysis. Paracetamol can be quantified by this method in the 1 μg L−1 to 300 μg L−1 concentration range. The limit of detection and limit of quantification in plasma samples are 0.17 and 0.4 μg L−1. The preconcentration factor of the m-MIPs is 40. The HPLC method shows good precision (4.5 % at 50 μg L−1 levels) and recoveries (between 83 and 91 %) from spiked plasma samples.
We are presenting magnetic molecularly imprinted polymer nanoparticles (m-MIPs) for solid-phase extraction and sample clean-up of paracetamol. The m-MIPs were applied to the extraction of paracetamol from human blood plasma samples
Hetero-dimeric magnetic nanoparticles of the type Au-Fe3O4 have been synthesised from separately prepared, differently shaped (spheres and cubes), monodisperse nanoparticles. This synthesis was achieved by the following steps: (a) Mono-functionalising each type of nanoparticles with aldehyde functional groups through a solid support approach, where nanoparticle decorated silica nanoparticles were fabricated as an intermediate step; (b) Derivatising the functional faces with complementary functionalities (e.g. amines and carboxylic acids); (c) Dimerising the two types of particles via amide bond formation. The resulting hetero-dimers were characterised by high-resolution TEM, Fourier transform IR spectroscopy and other appropriate methods.
Graphical Abstract Nano-LEGO: Assembling two types of separately prepared nanoparticles into a hetero-dimer is the first step towards complex nano-architectures. This study shows a solid support approach to combine a gold and a magnetite nanocrystal.
Graphite-like carbon nitride ? Fe3O4 magnetic nanocomposites were synthesized by a chemical co-precipitation method. The nanocomposites were characterized by transmission electron microscopy, X-ray diffraction, FTIR spectroscopy, X-ray photoelectron spectroscopy and magnetization hysteresis loops. The nanocomposites exhibit enhanced peroxidase-like activity (compared to that of graphite-like carbon nitride or Fe3O4 NPs). More specifically, they are capable of catalyzing the oxidation of different peroxidase substrates (such as TMB, ABTS or OPD) by H2O2 to produce the typical color reactions (blue, green or orange). The nanocomposites retain their magnetic properties and can be separated by an external magnet. On the basis of these findings, a highly sensitive and selective method was applied to the determination of H2O2 and glucose (by using glucose oxidase). It was successfully applied to the determination of glucose in (spiked) human serum. Compared to other nanomaterial-based peroxidase mimetics, the one described here provides distinctly higher sensitivity for both H2O2 and glucose, with detection limits as low as 0.3 μM and 0.25 μM, respectively.
Graphical abstract The magnetic carbon nitride nanocomposite exhibits enhanced peroxidase-like activity that is much larger than that of graphite-like carbon nitride or Fe3O4 NPs alone. This finding was applied to design a highly sensitive and selective colorimetric assay for H2O2 and glucose.
