Developing an exclusive sensor based on molecularly imprinted polymer/Multi-walled carbon nanotubes/Fe3O4@Au nanocomposite for the selective determination of an anti-cancer drug imatinib.

Determination of pharmaceuticals especially anticancer drugs is one of the important issues in environmental and medical investigation and creating good information about human health. The presence sturdy introducing an electroanalytical sensor based on molecularly imprinted polymer (MIP)/Multi-walled carbon nanotubes (MWCNTs)/Au@Fe3O4 nanoparticles modified carbon paste electrode (PE) to determine imatinib (IMA). The MIP/MWCNTs/Au@Fe3O4/PE showed catalytic activity and also a sensitive strategy to sensing IMA in the concentration range 1-1000 µM with a limit of detection of 0.013 µM. The MIP/MWCNTs/Au@Fe3O4/PE has shown interesting results in the analysis of IMA in real samples, and the interference investigations results show the high selectivity of the MIP/MWCNTs/Au@Fe3O4/PE in the monitoring of IMA in complex fluids such as tablet and blood serum and results approved by F-test and t-test as statistical methods.

Nanohybrid of antimonene@Ti3C2Tx-based electrochemical aptasensor for lead detection.

Lead ions (Pb2+), as one of many common heavy metallic environmental pollutants, can cause serious side-effects and result in chronic poisoning to people's health, so it is highly significant to monitor Pb2+ efficiently and sensitively. Here, we proposed an antimonene@Ti3C2Tx nanohybrid-based electrochemical aptamer sensor (aptasensor) for high sensitive Pb2+ determination. The sensing platform of nanohybrid was synthesized by ultrasonication, possessing the advantages of both antimonene and Ti3C2Tx, which not only can vastly enlarge the sensing signal of the proposed aptasensor, but also greatly simplified its manufacturing flow, because antimonene can strongly interact with aptamer through noncovalently bound. The surface morphology and microarchitecture of the nanohybrid were perused by several methods such as scanning electron microscope (SEM), energy-dispersive X-ray mapping spectroscopy (EDS), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and atomic force microscope (AFM). Under optimal empirical conditions, the proposed aptasensor exhibited a wide linear correlation of the current signals with the logarithm of CPb2+ (Log CPb2+) over the span from 1 × 10-12 to 1 × 10-7 M and provided a trace discernment limit of 3.3 × 10-13 M. Moreover, the constructed aptasensor displayed superior repeatability, great consistency, eminent selectivity, and beneficial reproducibility, implying its extreme potential application for water quality control and the environmental monitoring of Pb2+.

Calf thymus ds-DNA intercalation with pendimethalin herbicide at the surface of ZIF-8/Co/rGO/C3N4/ds-DNA/SPCE; A bio-sensing approach for pendimethalin quantification confirmed by molecular docking study.

Pendimethalin (PND) is a herbicide that is regarded to be possibly carcinogenic to humans and toxic to the environment. Herein, we fabricated a highly sensitive DNA biosensor based on ZIF-8/Co/rGO/C3N4 nanohybrid modification of a screen-printed carbon electrode (SPCE) to monitor PND in real samples. The layer-by-layer fabrication pathway was conducted to construct ZIF-8/Co/rGO/C3N4/ds-DNA/SPCE biosensor. The physicochemical characterization techniques confirmed the successful synthesis of ZIF-8/Co/rGO/C3N4 hybrid nanocomposite, as well as the appropriate modification of the SPCE surface. The utilization of ZIF-8/Co/rGO/C3N4 nanohybrid as a modifier was analyzed using. The electrochemical impedance spectroscopy results showed that the modified SPCE exhibited significantly lowered charge transfer resistance due to the enhancement of its electrical conductivity and facilitation of the transfer of charged particles. The proposed biosensor successfully quantified PND in a wide concentration range of 0.01-35 µM, with a limit of detection (LOD) value of 8.0 nM. The PND monitoring capability of the fabricated biosensor in real samples including rice, wheat, tap, and river water samples was verified with a recovery range of 98.2-105.6%. Moreover, to predict the interaction sites of PND herbicide with DNA, the molecular docking study was performed between the PND molecule and two sequence DNA fragments and confirmed the experimental findings. This research sets the stage for developing highly sensitive DNA biosensors that will be used to monitor and quantify toxic herbicides in real samples by fusing the advantages of nanohybrid structures with crucial knowledge from a molecular docking investigation.

A Modified Electrochemical Sensor Based on N,S-Doped Carbon Dots/Carbon Nanotube-Poly(Amidoamine) Dendrimer Hybrids for Imatinib Mesylate Determination.

Imatinib mesylate, an anticancer drug, is prescribed to treat gastrointestinal stromal tumors and chronic myelogenous leukemia. A hybrid nanocomposite of N,S-doped carbon dots/carbon nanotube-poly(amidoamine) dendrimer (N,S-CDs/CNTD) was successfully synthesized and used as a significant modifier to design a new and highly selective electrochemical sensor for the determination of imatinib mesylate. A rigorous study with electrochemical techniques, such as cyclic voltammetry and differential pulse voltammetry, was performed to elucidate the electrocatalytic properties of the as-prepared nanocomposite and the preparation procedure of the modified glassy carbon electrode (GCE). A higher oxidation peak current was generated for the imatinib mesylate on a N,S-CDs/CNTD/GCE surface compared to the GCE and CNTD/GCE. The N,S-CDs/CNTD/GCE showed a linear relationship between the concentration and oxidation peak current of the imatinib mesylate in 0.01-100 µM, with a detection limit of 3 nM. Finally, the imatinib mesylate's quantification in blood-serum samples was successfully performed. The N,S-CDs/CNTD/GCE's reproducibility and stability were indeed excellent.

Engineering and application of polysaccharides and proteins-based nanobiocatalysts in the recovery of toxic metals, phosphorous, and ammonia from wastewater: A review.

Global waste production is anticipated reach to 2.59 billion tons in 2030, thus accentuating issues of environmental pollution and health security. 37 % of waste is landfilled, 33 % is discharged or burned in open areas, and only 13.5 % is recycled, which makes waste management poorly efficient in the context of the circular economy. There is, therefore, a need for methods to recycle waste into valuable materials through the resource recovery process. Progress in the field of recycling is strongly dependent on the development of efficient, stable, and reusable yet inexpensive catalysts. In this case, growing attention has been paid to the development and application of nanobiocatalysts with promising features. The main purpose of this review paper is to: (i) introduce nanobiomaterials and describe their effective role in the preparation of functional nanobiocatalysts for the recourse recovery aims; (ii) provide production methods and the efficiency improvement of nanobaiocatalysts; (iii) give a comprehensive description of valued resource recovery for reducing toxic chemicals from the contaminated environment; (iv) describe various technologies for the valued resource recovery; (v) state the limitation of the valued resource recovery; (vi) and finally economic importance and current scenario of nanobiocatalysts strategies applicable for the resource recovery processes.

Highly effectual photocatalytic degradation of tartrazine by using Ag nanoparticles decorated on Zn-Cu-Cr layered double hydroxide@ 2D graphitic carbon nitride (C3N5).

Pollution of water resources is one of the main concerns of many countries. This issue originates from the entry of diverse pollutants, including dye compounds, into water sources. In this work, ternary Zn-Cu-Cr layered double hydroxides (LDH) supported on graphitic carbon nitride (g-C3N5) decorated by silver nanoparticles (C3N5-LDH-Ag) was first prepared. Application of various characterization techniques such as SEM, XRD, and FT-IR revealed that the synthesized nanocomposite was composed of Zn-Cu-Cr LDH nanoparticles, g-C3N5 nanosheets, and Ag nanoparticles. The prepared nanomaterials were employed for the photodegradation of tartrazine in aqueous solutions. It was found that the C3N5-LDH-Ag catalyst outperformed their pure g-C3N5, Zn-Cu-Cr LDH, and C3N5-LDH composite in photocatalytic degradation of tartrazine under visible light irradiation. Tartrazine (20 mg/L) can be entirely removed by 0.25 g/L C3N5-LDH-Ag photocatalyst under 1 h visible light irradiation (200 W) at pH 6 with a rapid degradation rate constant (k) that is 4.4, 3.9, and 2.6 times higher than that of pure C3N5, Zn-Cu-Cr LDH, and C3N5-LDH component, respectively. The formation of hydroxyl radicals on the surface of C3N5-LDH-Ag as the main active species was approved by the capturing experiment. The finding results approved the stability and reusability of C3N5-LDH-Ag in four photocatalytic degradation cycles. In general, our findings revealed that the synthesized nanocomposite could be employed as an efficient photocatalyst in environmental remediation.

Preparation of a Highly Sensitive Electrochemical Aptasensor for Measuring Epirubicin Based on a Gold Electrode Boosted with Carbon Nano-Onions and MB.

Epirubicin is prescribed as an essential drug for treating breast, prostate, uterine, and gastrointestinal cancers. It has many side effects, such as heart failure, mouth inflammation, abdominal pain, fever, and shortness of breath. Its measurement is necessary by straightforward and cheap methods. The application of aptamer-based electrochemical sensors is accounted as a selective option for measuring different compounds. In this work, a thiol-modified aptamer was self-assembled on the surface of the gold electrode (AuE) boosted with carbon nano-onions (CNOs), and coupled with methylene blue (MB) as an electroactive tracker to achieve a sensitive and selective aptasensor. In the absence of the epirubicin, CNOs binds to the aptamer through a π-π interaction enhancing the MB electrochemical signal. When epirubicin binds to the aptamer, the adsorption of CNOs and MB to the aptamer is not well established, so the electrochemical signal is reduced, consequently, the epirubicin value can be measured. The prepared aptasensor demonstrated an excellent sensitivity with a curve slope of 0.36 µI/nM, and 3 nM limit of detection in the linear concentration range of 1-75 nM. The prepared aptasensor was accurately capable of measuring epirubicin in blood serum samples.

Fabrication of sensor based on polyvinyl alcohol functionalized tungsten oxide/reduced graphene oxide nanocomposite for electrochemical monitoring of 4-aminophenol.

4-aminophenol (4-AP) is one of the major environmental pollutants which is broadly exploited as drug intermediate in the pharmaceutical formulations. The extensive release of 4-AP in the environment without treatment has become a serious issue that has led several health effects on humans. This work describe the determination of 4-AP through a new chemically modified sensor based on polyvinyl alcohol functionalized tungsten oxide/reduced graphene oxide (PVA/WO3/rGO) nanocomposite. The fabricated nanocomposite was characterized through XRD and HR-TEM to confirm the crystalline structure with average size of 35.9 nm and 2D texture with ultra-fine sheets. The electrochemical characterization of fabricated sensor was carried out by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) to ensure the charge transfer kinetics of modified sensor that revealed high conductivity of PVA/WO3/rGO/GCE. Under optimized conditions e.g. scan rate 80 mV/s, phosphate buffer (pH 6) as supporting electrolyte and potential window from -0.2 to 0.8 V, the prepared sensor showed excellent response for 4-AP. The linear dynamic range of developed method was optimized as 0.003-70 µM. The LOD of fabricated sensor based on PVA/WO3/rGO/GCE for 4-AP was calculated as 0.51 nM. The practical application of PVA/WO3/rGO/GCE was tested in real water and pharmaceutical samples. The fabricated sensor presented here, exhibited exceptional stability and sensitivity than the reported sensors and could be effectively used for the monitoring 4-AP without interferences.

Evaluation of MXene as an adsorbent in dispersive solid phase extraction of several pesticides from fresh fruit juices prior to their determination by HPLC-MS/MS.

This study aimed to introduce a dispersive solid phase extraction method based on MXene nanoparticles as a novel sorbent for the simultaneous extraction and determination of twelve pesticides from fresh fruit juices. In the following, a high performance liquid chromatography-tandem mass spectrometry was used for their determination in the samples. In this method, two-dimensional nanomaterials of Ti2AlC were exfoliated in an acidic solution and then they were added into the sample solution. To enhance the sample solution and sorbent contact area, the mixture was vortexed for a few minutes. Then the adsorbed analytes onto the sorbent were eluted using acetone and then analyzed. Under optimal conditions, the calibration curves of the method were linear within the range of 3.0-1000 µg L-1. The limits of detection, intra- and inter-day relative standard deviations, and extraction recoveries were in the ranges of 0.08-1.0 µg L-1, 2.5-4.2%, 2.5-5.5%, and 69-75%, respectively. Performing the method verified the presence of some of the analytes in several samples. This method can help to monitor pesticides in juice samples as well as to improve our understanding the safety of foods.

Architecting of an aptasensor for the staphylococcus aureus analysis by modification of the screen-printed carbon electrode with aptamer/Ag-Cs-Gr QDs/NTiO2.

Given the many issues bacterial infections cause to humans and the necessity for their detection, in this work we developed a robust aptasensor for prompt, ultrasensitive, and selective analysis of staphylococcus aureus bacterium (S. aureus). A nanocomposite of Ag nanoparticles, chitosan, graphene quantum dots, and nitrogen-doped TiO2 nanoparticles (Ag-Cs-Gr QDs/NTiO2) was synthesized, and thoroughly characterized by XRD, FT-IR, and FE-SEM spectroscopic methods. The surface of screen-printed carbon electrodes modified with Ag-Cs-Gr QDs/NTiO2 nanocomposite was utilized as a compatible platform for aptamer attachment. The aptasensor accurately determined S. aureus in the dynamic range of 10-5 × 108 CFU/mL with detection limit of 3.3 CFU/mL. The monitoring of the practical performance of aptasensor in human serum samples revealed its superiority over the conventional methods (relative recovery of 96.25-103.33%). The Ag-Cs-Gr QDs/NTiO2-based aptasensor offers facile, biocompatibility, good repeatability, reproducibility (RSD = 3.66%), label free and stabile strategy for sensitive S. aureus analysis free from biomolecules interferences in actual specimens.

Recent advances in Ponceau dyes monitoring as food colorant substances by electrochemical sensors and developed procedures for their removal from real samples.

Ponceau dyes are one of the food coloring materials that are added to various pharmaceutical, health and food products and give them an appearance. These dyes contain contaminants such as Benzidine, 4-Aminobiphenyl, and 4-Aminoazobenzene that are safe in small amounts, but they are not approved by the US Food and Drug Administration (US-FDA) for human consumption. This study comprehensively was reviewed the properties, applications, chemistry, and toxicity of Ponceau dyes as food colorant substances. Electroanalysis of Ponceau dyes was discussed in detail, and the various electrochemical sensors used to detect and monitor these dyes as food colorant were examined. The applied methods of removing and degradation of these dyes in municipal and industrial wastes were also discussed. Conclusions and future perspectives to motivate future research were also explored.

Application of Nanomaterials in Development of Electrochemical Sensors and Drug Delivery Systems for Anticancer Drugs and Cancer Biomarkers.

Worldwide occurrence of cancer has initiated a global effort for the development and production of various anticancer drugs. Unfortunately, high potential toxicity and mutagenic and carcinogenic side effects have been reported for most of the anticancer drugs, which cause many problems for the patient even at a slight dosage. Considering this, thanks to their outstanding features such as high sensitivity, selectivity, and cheapness, electrochemical methods have received much attention in the development of quick, precise, and reliable (bio) sensors for the monitoring of anticancer drugs and cancer biomarkers. Here, procedures and approaches presented for the development of modified electrodes based on nanomaterials employed for the anticancer drugs and cancer biomarkers sensing are reviewed. The analytical performance of the constructed electrodes including physical and electrochemical properties together with their figures of merits is highlighted. Nanomaterials offer excellent features for anticancer drugs. They improve multi-drug resistance, site-specificity and enhance efficient delivery. The premature degradation, preventing interaction with biological systems, absorption of the drugs into the selected tissues, controlling of the pharmacokinetic properties and skipping distribution profile can be performed with nanomaterials. In this review, detailed features of nanomaterials in anticancer drug delivery systems will be presented together with the application of nanomaterials in electrochemical sensors.

Green synthesis of nonprecious metal-doped copper hydroxide nanoparticles for construction of a dopamine sensor.

Background: Copper oxide nanoparticles doped with nonprecious metal species (Ni and Mn) were synthesized. Method: A glassy carbon electrode (GCE) was modified by drop-casting of nanostructure suspensions, constructing Ni:Cu(OH)2/GCE, Mn:Cu(OH)2/GCE and Cu(OH)2/GCE. Results: The voltammetric oxidation of dopamine (DA) by the constructed electrodes confirmed that the electrocatalytic oxidation of DA is a reversible, pH-dependent, diffusion-controlled process; the best response was obtained by Mn:Cu(OH)2/GCE. A sensitive calibration graph (0.664 µA/µM) was produced for DA in the concentration range of 0.3-10.0 µM, with a detection limit of 79 nM using Mn:Cu(OH)2/GCE. Conclusion: The Mn:Cu(OH)2/GCE possessed an accurate response toward DA with an acceptable selectivity, stability and antifouling effect, revealing the applicability of the Mn:Cu(OH)2/GCE for DA analysis in biological samples.

A noble electrochemical sensor based on TiO2@CuO-N-rGO and poly (L-cysteine) nanocomposite applicable for trace analysis of flunitrazepam.

Flunitrazepam or date rape medication with trade name of Rohypnol belongs to the benzodiazepines branch that is used as a sedative, anesthetic, anticonvulsant, muscle relaxant, and antianxiety drug. It is known as "drug of aggression" because of its very strong and long-lasting effects on the central nervous system. The sedative influence of flunitrazepam drug increases with alcohol drinking, which causes mental and motor disorders and causes the victim to become silent. Due to its criminals use, its accurate measurement is crucial. In this work, a novel electrochemical sensor based on TiO2@CuO-N doped rGO, TiO2@CuO-N-rGO, nano-composite and poly (L-cysteine), poly (L-Cys), is presented for trace analysis of flunitrazepam in aqueous solution. At first, TiO2@CuO-N-rGO nano-composite was synthesized by the sol-gel method and characterized by Raman spectroscopy, Fourier transform infrared, field emission scanning electron microscope, and X-ray diffraction analysis. Then, the suspension of the TiO2@CuO-N-rGO nano-composite was drop casted on the surface of the glassy carbon electrode (GCE/TiO2@CuO-N-rGO). After that, electro-polymerization of l-cysteine on the GCE/TiO2@CuO-N-rGO surface was performed by cyclic voltammetry (CV) method. The electrochemical characteristics of the GCE/TiO2@CuO-N-rGO/poly (L-Cys) surface were evaluated in the solution of ferri/ferrocyanide by electrochemical impedance spectroscopy (EIS) and CV techniques. The increase in current, change in oxidation peak potential, and the appearance of two reduction peaks indicated higher electron transfer rate with well-performed electrochemical process of flunitrazepam at the modified electrode surface compared to the bare GCE. These improvements originate from the synergistic effect of TiO2@CuO-N-rGO nano-composite and poly (L-Cys). Finally, a linear relationship was resulted between the oxidation peak current and the concentration of flunitrazepam in the wide concentration range of 1 nM to 50 µM with a detection limit of 0.3 nM.

Withdrawal Notice: Application of Nanomaterials in Development of Electrochemical Sensors and Drug Delivery Systems for Anticancer Drugs

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Combination of Efficiency with Easiness, Speed, and Cheapness in Development of Sensitive Electrochemical Sensors.

Nowadays, electrochemical techniques can be considered as a suitable alternative technique besides UV/Vis spectroscopy, liquid chromatography, capillary electrophoresis, mass spectroscopy, NMR for evaluation and determination of different electroactive compounds. Solid electrodes such as carbon and metal-based substrates are common for electrochemical applications. Especially, during two past decades, different types of modified electrodes with these solid electrodes have been developed for fast, sensitive, and selective analysis of various important analyses (biomolecules, enzymes, and drugs) in a wide range of real samples. These applications are highly efficient, cost effective and facile fabrication procedures of the electrode modification can be employed. In the present review, at first, some recently developed high performance bare and modified electrodes are evaluated based on their outstanding properties. In the next step, developed new procedures or fabricated modified electrodes with good sensitivity based on simple and cheap protocols are introduced and discussed.

Development of Carbon Nanostructured Based Electrochemical Sensors for Pharmaceutical Analysis.

Pharmaceutical drugs play an important role in human life since they caused a revolution in human health. Notably, their administration to a living organism helps body to stay healthy. Commonly, they are employed to diagnose, prevent, or treat and cure a disease via a biological effect on a human body. Administration of impurity-free and adequate amounts of pharmaceutical compounds would be beneficial. Therefore, the quantity and purity of the substances in pharmaceutical compounds are continuously monitored during drug manufacturing with various chemical or instrumental analysis techniques. The possibility of impurities development and chemical or quantity changes of active drug species at various stages (namely during production, transportation or storage) makes them redundant and risky for human health. So, sensitive and accurate analysis methods for qualitative and quantitative analysis are highly demanded by pharmaceutical companies and medical centers. The present mini review emphasizes on application of carbon based modified electrodes in health care and pharmaceutical analysis. Electrochemical determination of drugs employing carbon nanostructured modified electrodes will be reviewed and their advantages and disadvantages will be mentioned.

Klonopin assay using modified electrode with multiwalled carbon nanotubes and poly melamine nanocomposite.

Developing of cheap, sensitive and stable sensors plays a significant role in pharmaceutical and clinical applications. Considering the effective role of Klonopin (KNP) in the treatment of epilepsy, KNP quantification in its production process for dose adjustments and checking the purity and also after its usage by patents for bioavailability testing and effectiveness assay is vital. In present work, an efficient electrochemical sensor based on poly melamine and multiwalled carbon nanotubes nanocomposite (PMela/CNTs) was constructed which displayed effective electrochemical response toward KNP. Electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV) and square-wave voltammetry (SWV) experiments were applied for performance evaluation of the PMela/CNTs modified electrode and electrochemical redox behavior of KNP. Distinguish synergetic effect was observed between CNTs and poly melamine in response to KNP electrochemical redox reaction. A linear detection range of 0.05 to 10 µM with the detection limits of 63 nM was achieved for KNP analysis. The practical application of the PMela/CNTs modified electrode revealed satisfactory results for quantification of KNP in biological fluids.

Study and Optimization of The Necessary Conditions for The Sensitive Determination of The Lead Ion by a Modified Carbon Paste Electrode in Environmental Water Samples.

Rapid and facile preparation of the cheap modified electrode materials is an important parameter in development of the efficient electrochemical sensor for industrial scale production and mass-market usage. In the present work, the carbon paste electrode modified with multi-walled carbon nanotubes (MWCNTs) was prepared for sensitive determination of lead (Pb) ion in the presence of bismuth (Bi) ion due to synergetic effect of carbon nano-materials and Bi on the voltammetric response. Investigations showed that in presence of Bi ion degassing of the test solution is not needed. Supporting electrolyte, required Bi concentration and accumulation time and potential were optimized for differential pulsed anodic stripping voltammetric tests. Under optimized conditions, modified carbon paste electrode showed sensitive voltammetric response in the range of 0.1-10 µM toward Pb ion. Moreover, efficiency of the developed method was evaluated for the determination of Pb ion in several water samples. The obtained recovery results of 92-97 % revealed good agreement between responses of this sensor and common spectroscopies techniques for the Pb ion analysis. The optimized system has high efficiency in reproducibility and repeatability of the results and applicability for the analysis of the various environmental water samples.

Electrochemical and DFT study of an anticancer and active anthelmintic drug at carbon nanostructured modified electrode.

The electrochemical response of mebendazole (Meb), an anticancer and effective anthelmintic drug, was investigated using two different carbon nanostructured modified glassy carbon electrodes (GCE). Although, compared to unmodified GCE, both prepared modified electrodes improved the voltammetric response of Meb, the carbon nanotubes (CNTs) modified GCE showed higher sensitivity and stability. Therefore, the CNTs-GCE was chosen as a promising candidate for the further studies. At first, the electrochemical behavior of Meb was studied by cyclic voltammetry and differential pulse and square wave voltammetry. A one step reversible, pH-dependent and adsorption-controlled process was revealed for electro-oxidation of Meb. A possible mechanism for the electrochemical oxidation of Meb was proposed. In addition, electronic structure, adsorption energy, band gap, type of interaction and stable configuration of Meb on the surface of functionalized carbon nanotubes were studied by using density functional theory (DFT). Obtained results revealed that Meb is weakly physisorbed on the CNTs and that the electronic properties of the CNTs are not significantly changed. Notably, CNTs could be considered as a suitable modifier for preparation of the modified electrode for Meb analysis. Then, the experimental parameters affecting the electrochemical response of Meb were optimized. Under optimal conditions, high sensitivity (b(Meb)=dIp,a(Meb)/d[Meb]=19.65µAµM(-1)), a low detection limit (LOD (Meb)=19nM) and a wide linear dynamic range (0.06-3µM) was resulted for the voltammetric quantification of Meb.