Selective Detection Of Dopamine Research Articles

Carbon quantum dots composite for enhanced selective detection of dopamine with organic electrochemical transistors

A compact organic electrochemical transistors (OECT) sensor enriched with carbon quantum dots (CQDs) was developed to enhance the transconductance of an electropolymerized poly(3,4-ethylenedioxythiophene) (PEDOT) film, enabling the precise and selective detection of dopamine (DA). Accurate monitoring of DA levels is critical for diagnosing and managing related conditions. Incorporating CQDs, we have achieved a remarkable up to threefold increase in current at the DA detection peak in differential pulse voltammetry. This enhancement showcases superior selectivity even in the presence of high concentrations of interferents like uric acid and ascorbic acid. This material significantly boosts the sensitivity of OECTs for DA detection, delivering an amperometric response with a detection limit of 55 nM and a broader detection range (1 − 500 µM). Our results underscore the potential of low-dimensional carbonaceous materials in creating cost-effective, high-sensitivity devices for detecting DA and other biomolecules. This breakthrough sets the stage for the development of next-generation biosensors for point-of-care diagnostics.Graphical

A dual-template molecularly imprinted electrochemical sensor assisted with BO-XGBoost algorithm for simultaneous determination of dopamine and acetaminophen

The simultaneous detection of dopamine (DA) and acetaminophen (AP) is crucial for diagnosing and treating related mental disorders. However, accurately determining DA and AP in biological samples remains challenging due to the interference from other biomolecules, such as ascorbic acid (AA), uric acid (UA), epinephrine (EP), etc. Here, we present a dual-template molecularly imprinted electrochemical sensor for the selective recognition of DA and AP. Reduced graphene(rGO)-gold nanoparticles(AuNPs) composite were utilized to enhance the effective area and increase the electron transfer rate of glassy carbon electrode(GCE), thus the electrochemical response signals were amplified. This sensor combined the advantages of nanocomposites and molecularly imprinted polymer (MIP) to achieve highly sensitive and selective detection of DA and AP. However, decreases in the current response of some analytes and variations in relationships of the peak current versus analyte concentration will occur due to adsorption competition on active sites in multianalyte mixtures, rendering the detection range constrained and traditional linear fitting methods inaccurate for predicting analyte concentrations. Therefore, a concentration prediction model based on XGBoost was developed for the sensor to achieve the reliable multi-component determination of DA and AP within the identical measurement range as individual detection. In this model, nine characteristic parameters were extracted from the differential pulse voltammetry (DPV) response curve and Bayesian optimization (BO) was adopted for automatic hyperparameter search, thereby the prediction errors were reduced and the generalization ability was improved. Experiments indicated that the MIP/AuNPs/rGO/GCE exhibited a wide detection range of 2–240 μM and 3–240 μM for DA and AP, with detection limits down to 0.26 μM and 0.33 μM, respectively. In addition, the intelligent MIP/AuNPs/rGO/GCE sensor based on BO-XGBoost model provides more accurate prediction results for untrained concentration combinations obtained from fetal bovine serum samples, indicating that the proposed detection scheme holds potential in future clinical diagnosis.

Flexible Organic Electrochemical Transistor Based on Conjugated Conducting Polymers

— The use of organic electrochemical transistors (OECTs) based on conjugated polymers has gained significant recognition owing to their impressive performance, flexibility, ease of fabrication, and suitability for specific applications where solid-state transistors may not be efficiently employed. Key advantages of OECT technology, such as simple device architecture, robustness in ambient or aqueous environments, straightforward additive manufacturing processes, low operational voltage, and compatibility with flexible, rough, stretchable, and large-area substrates, underscore its significance in various applications. These applications span the sensing of glucose [1], bacteria [2], dopamine [3], DNA [4], lactate [5], cell activities [6], and electrophysiological signals [7]. Notably, the absence of the necessity for a reference electrode, a crucial feature for wearable and textile sensors compared to three electrode-based electrochemical sensors, stands out. In this context, we have fabricated a side-gated OECT on a flexible polyethylene terephthalate (PET) substrate through a scalable screen-printing process where the source, drain, and gate terminals are screen-printed using silver (Ag) conductive ink. The semiconducting channel material employed is polyethylene dioxythiophene: polystyrene sulfonate (PEDOT: PSS), which is spin-coated. Additionally, poly methyl methacrylate (PMMA) has been spin-coated to serve as the dielectric. The OECT operates by volumetric gating of the channel through a gel electrolyte containing poly sodium 4-styrene sulfonate (PSSna), enabling polarization of the gate and channel to induce charge accumulation or depletion, driven by the application of a gate-source voltage. The OECT device structure demonstrated switching from the "ON" to "OFF” state with the application of a positive gate voltage, indicating its functionality as a p-type depletion mode transistor. Additionally, the OECT displayed a transconductance (gm) of 6.25×10-4 A/V, mobility (µ) of 1.242×1010 cm2 /Vs, and a threshold voltage (Vth) of -0.39 V, with the on/off ratio being relatively low at 7.22. The repeatability was confirmed through the fabrication of three devices that exhibited nearly identical behavior. Furthermore, in pursuit of faster response time, lower operating voltage, and miniaturization, additional work involves downscaling the active area length to 100µm from the reported 4mm active area length. The fabrication method not only holds the capability for large-scale production with a high yield in a cost-effective manner but also opens up possibilities for applications requiring swift design changes and digitally enabled direct-write techniques. Future work emphasizes functionalizing the electrolyte used in OECT to detect biomolecules such as glucose, pH, and ion species. Thus, this research underscores the potential usability of fabricated OECTs in various high-performance chemical and biological sensing applications. REFERENCES Tang, H.; Yan, F.; Lin, P.; Xu, J.; Chan, H.L.W. Highly Sensitive Glucose Biosensors Based on OrganicElectrochemical Transistors Using Platinum Gate Electrodes Modified with Enzyme and Nanomaterials.Adv. Funct. Mater. 2011, 21, 2264–2272. [CrossRef]He, R.-X.; Zhang, M.; Tan, F.; Leung, P.H.M.; Zhao, X.-Z.; Chan, H.L.W.; Yang, M.; Yan, F. Detection of bacteria with organic electrochemical transistors. J. Mater. Chem. 2012, 22, 22072–22076. [CrossRef]Gualandi, I.; Tonelli, D.; Mariani, F.; Scavetta, E.; Marzocchi, M.; Fraboni, B. Selective detection of dopamine with an all PEDOT:PSS Organic Electrochemical Transistor. Sci. Rep. 2016, 6, 35419. [CrossRef]Tao, W.; Lin, P.; Hu, J.; Ke, S.; Song, J.; Zeng, X. A sensitive DNA sensor based on an organic electrochemical transistor using a peptide nucleic acid-modified nanoporous gold gate electrode. RSC Adv. 2017, 7, 52118–52124. [CrossRef]Braendlein, M.; Pappa, A.-M.; Ferro, M.; Lopresti, A.; Acquaviva, C.; Mamessier, E.; Malliaras, G.G. Owens, R.M. Lactate Detection in Tumor Cell Cultures Using Organic Transistor Circuits. Adv. Mater. 2017, 1605744.Lin, P.; Yan, F.; Yu, J.; Chan, H.L.W.; Yang, M. The Application of Organic Electrochemical Transistors in Cell-Based Biosensors. Adv. Mater. 2010, 22, 3655–3660Liang, Y.; Ernst, M.; Brings, F.; Kireev, D.; Maybeck, V.; Offenhäusser, A.; Mayer, D. High Performance Flexible Organic Electrochemical Transistors for Monitoring Cardiac Action Potential. Adv. Healthc. Mater. 2018, 1800304. [CrossRef] Figure 1

Real samples sensitive dopamine sensor based on poly 1,3-benzothiazol-2-yl((4-carboxlicphenyl)hydrazono)acetonitrile on a glassy carbon electrode

Herein, a novel electrochemical sensor that was used for the first time for sensitive and selective detection of dopamine (DA) was fabricated. The new sensor is based on the decoration of the glassy carbon electrode surface (GC) with a polymer film of 1,3-Benzothiazol-2-yl((4-carboxlicphenyl)hydrazono)) acetonitrile (poly(BTCA). The prepared (poly(BTCA) was examined by using different techniques such as 1H NMR, 13C NMR, FTIR, and UV-visible spectroscopy. The electrochemical investigations of DA were assessed using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The results obtained showed that the modifier increased the electrocatalytic efficiency with a noticeable increase in the oxidation peak current of DA in 0.1 M phosphate buffer solution (PBS) at an optimum pH of 7.0 and scan rate of 200 mV/s when compared to unmodified GC. The new sensor displays a good performance for detecting DA with a limit of detection (LOD 3σ), and limit of quantification (LOQ 10σ) are 0.28 nM and 94 nM respectively. The peak current of DA is linearly proportional to the concentration in the range from 0.1 to 10.0 µM. Additionally, the fabricated electrode showed sufficient reproducibility, stability, and selectivity for DA detection in the presence of different interferents. The proposed poly(BTCA)/GCE sensor was effectively applied to detect DA in the biological samples.

Bipolar electrochemical sensor with perylene diimide-based cathodic luminophore for dopamine detection and imaging

Bipolar electrochemical microscopy (BEM), which visualizes the concentration distribution of molecular species in biological systems by electrochemiluminescence (ECL), is expected to be applied to the high-spatiotemporal-resolution imaging of biomolecules, enabling the analysis of cellular functions. In the past, the molecular species that could be imaged by BEM were generally restricted to oxidized molecules due to the limitation derived from the ECL mechanism of the luminophore. Recently, the imaging of dopamine (DA), a reduced molecule, was achieved using Ru (bpy)32+/glutathione disulfide (GSSG) as a cathodic luminophore. However, a large driving voltage was required for ECL generation, resulting in a low S/N ratio. In this study, we employed N,N′-dimethyl-3,4,9,10-perylenetetracarboxylic diimide (PDI-CH3)/potassium peroxodisulfate (K2S2O8), which is a cathodic luminophore that can be reduced at a nobler potential to produce ECL than [Ru(bpy)3]2+/GSSG. First, the ECL mechanism of PDI-CH3/K2S2O8 was elucidated by using a PDI-CH3 drop-cast glassy carbon electrode (GCE) immersed in K2S2O8 solution as the working electrode in a 3-electrode system. The PDI-CH3 drop-casted GCE, a single closed bipolar electrode (c-BPE), was used as the cathode in the successful quantification of 50–500 μmol L−1 DA in a sample chamber in which a c-BPE anode was immersed, resulting in a high S/N. The selective detection of DA in the presence of ascorbic acid was achieved by modifying the anode with Nafion. Finally, DA imaging was demonstrated using a commercially available anisotropic conducting film with PDI-CH3 coating on the cathode surface as a c-BPE array. The change in the concentration distribution in the inflow of DA was successfully imaged based on the change in the ECL intensity at the c-BPE cathode. This BEM system is expected to be useful for DA imaging of the brain.

Engineering FeOOH/Fe2O3@Carbon Interfaces With Biomass-Derived Carbon Nanodot/Iron Colloids for Efficient Redox-Modulated Dopamine Voltammetric Detection.

The Fe2+/Fe3+ redox couple is effective for voltammetric detection of trace dopamine (DA). However, achieving adequate concentrations with high electroactive surface area (ECSA), DA affinity, and fast interfacial charge transfer is challenging. Consequently, most reported Fe-based sensors have a high nanomolar range detection limit (LOD). Herein, we address these limitations by manipulating the phase and morphology of FeOOH/Fe2O3 heterojunctions anchored on sp2-carbon. FeOOH/Fe2O3 is synthesized by variable temperature aging of unique Fe5H9O15/Fe2O3@sp2-carbon colloidal nanoparticles, which form via chelation between biomass-derived carbon nanodots (CNDs) and Fe2+ ions. At 27 °C and 120 °C, Fe5H9O15/Fe2O3@sp2-carbon transforms into β-FeOOH/Fe2O3 nanoparticles and α-FeOOH/Fe2O3 nanosheet, respectively. The β-FeOOH/Fe2O3 interface exhibits higher eg orbital electron occupancy than α-FeOOH/Fe2O3, thereby facilitating oxygen adsorption and the generation of Fe2+/Fe3+ sites near the polarization potential of DA. This facilitates interfacial electron transfer between Fe3+ and DA. Moreover, its nanoparticle morphology enhances ECSA and DA adsorption compared to α-FeOOH/Fe2O3 nanosheets. With a LOD of ~3.11 nM, β-FeOOH/Fe2O3 surpasses the lower threshold in humans (~10 nM) and matches noble-metal sensors. Furthermore, it exhibits selective detection of DA over 10 biochemicals in urine. Therefore, the β-FeOOH/Fe2O3@sp2-C platform holds promise as a low-cost, easy-to-synthesize, and practical voltammetric DA monitor.

Polyvinylpyrrolidone‐Stabilized Blue‐Emitting Copper Nanoclusters as Fluorescence Probe for Selective Detection of Dopamine

AbstractDopamine (DA), a critical catecholamine in mammals, functions as a significant biological indicator for specific diseases. The precise and timely identification of DA is essential for disease monitoring and prevention. In this study, copper nanoclusters (Cu NCs) were synthesized using polyvinyl pyrrolidone (PVP) as the protective ligand and L‐ascorbic acid (L‐AA) as the reducing agent via a simple hydrothermal process. The produced PVP−Cu NCs displayed strong blue emission at 427 nm when excited at 365 nm. In alkaline conditions, DA was able to selectively inhibit the fluorescence of PVP−Cu NCs. The investigation of the mechanism revealed that dopamine self‐polymerization resulted in the formation of polydopamine, which inhibited the emission of PVP−Cu NCs at 427 nm due to the inner filter effect (IFE). Based on the above phenomenon, a simple and selective analytical method for DA determination was developed. The fluorescence intensity of PVP−Cu NCs demonstrated a reliable response to DA concentrations within the range of 5 to 200 μM, with a detection limit (LOD) of 1.32 μM. The proposed method was successfully utilized for the precise detection of DA in human urine samples, indicating its potential application in biomedical dopamine detection.

Development of Electrochemical and Colorimetric Biosensors for Detection of Dopamine

Neurotransmitters are essential chemical messengers required for proper brain function, and any changes in their concentrations can lead to neuronal diseases. Therefore, sensitive and selective detection is crucial. This study presents a fast and simple colorimetric method for dopamine detection using three reagent solutions: AgNP and MPA, Ag/Au nanocomposite, and mercaptophenylacetic acid. TEM images showed a narrow distribution of Ag and Au nanoparticles with average sizes of 20 nm and 13 nm, respectively, with gold nanoparticles bound to the edges of silver nanoparticles. A paper-based biosensor was created using manual wax printing for the colorimetric detection of dopamine. Visual detection onsite showed color changes with both the silver nanoparticles and mercaptophenylacetic acid mixture and the silver–gold nanoparticle composite. Electrochemical detection using a glassy carbon electrode modified with 8 mM mercaptophenylacetic acid demonstrated high selectivity and sensitivity towards dopamine, with a peak in the range of 0.7–0.9 V. Interferences were minimized, ensuring high sensitivity and selective detection of dopamine.

Highly sensitive and selective detection of dopamine using atomic layer deposited HfO2 ultra-thin films

The development of non-enzymatic and binder-free biosensors plays a vital role, and it possesses main benefits for effective biomolecule recognition with high sensitivity and preferred selectivity. Herein, an atomic layer deposition (ALD) was employed to develop the hafnium oxide (HfO2) nanofilm on silicon (Si) for fabricating binder-free selective and sensitive determination of the non-enzymatic electrochemical dopamine sensor. The prepared HfO2 nanofilm selectively acted as a local dopamine binding site because of the hydrophobic-hydrophobic interaction between fabricated film and dopamine, electrostatic attraction between negatively charged hydroxyl group on film surfaces, and positively charged amino group of dopamine. The developed insufficient oxygen vacancies on the HfO2 could have behaved as a charge-trapping site for better sensing properties. The developed sensor demonstrated excellent realization in sensing dopamine with a very low detection limit (0.4 pM) and swift response time of 3s which is quite precise compared with various reported literature. The fabricated HfO2/Si electrode sensor has exhibited high sensitivity, stability, and repeatability. The selectivity of dopamine sensors was at least three orders greater than other interfering biomolecules. This work proposes the essential track for the practical realization of dopamine detection in human serum and biomedical applications.

Oxygen-deficiency induced fluorescence nanosensor (ODIFN): Synthesis of Two-Dimensional NayWO4-x·2H2O nanosheets and its application in dopamine detection

Oxygen-deficiency induced fluorescence nanosensor (ODIFN) method applied in the Two-Dimensional nanosheets has been demonstrated in this paper. In this approach, we synthesized the abundant oxygen-deficient Two-Dimensional (2D) NayWO4-x·2H2O nanosheets fluorescence sensors and applied them for highly sensitive and selective dopamine detection. Researchers have been intensively motivated to create novel nanomaterials that enable the effective detection of dopamine (DA) in clinical samples. DA is a significant biomarker for various brain-related diseases such as Parkinson’s disease. We developed 2D NayWO4-x·2H2O nanosheets that exhibited a stable fluorescence emission at λem 360 nm. The non-stochiometric Na presenting in 2D nanosheets acts as a defecting agent for oxygen deficiency that results in strong and stable fluorescence. The fabricated fluorescence nanosheets were exhibited for the detection of dopamine with high sensitivity and selectivity. The ODIFN demonstrated a linear range of detection from 50 nM to 2 µM with a limit of detection of 0.31 nM and a very high R2 value of 0.996. Moreover, the sensor performance was evaluated in a biological fluid (blood serum) with results of R2 value of 0.995, which proves the high potential of NayWO4-x·2H2O nanosheets in DA sensing. The ODIFN via the 2D NayWO4-x·2H2O fluorescent sensor is a novel platform for producing artificial fluorescence that can be widely applied in all fields such as medical, biological, and life science fields to replace the traditional dyes that are highly harmful to environments.

Facile preparation of arginine-based carbon dots for highly selective detection of dopamine

Arginine-based carbon dots (Arg-CDs) were synthesized through a facile one-step hydrothermal method using arginine and urea as precursors. The as-prepared Arg-CDs displayed good aqueous solubility and typical excitation-dependent emission property, with the fluorescence quantum yield of 25.47 %. The fluorescence of Arg-CDs was gradually quenched by the addition of dopamine (DA) in the alkaline solution. However, under neutral and acidic condition, the fluorescence intensity of Arg-CDs remained unchanged upon the addition of DA. The sensing mechanism was probably due to the rapid oxidation of DA to dopaquinone in alkaline condition, which could quench the fluorescence of Arg-CDs through the Inner Filter Effect (IFE). Moreover, the fluorescence change of Arg-CDs was proportional to the concentration of DA under the optimized condition. Because of the linear relationship, the detection limit of dopamine was calculated to be 0.28 μM with the detection range from 10 to 100 μM. The interference experiment was carried out to further verify the specificity of this fluorometric method. Finally, the fluorometry based on Arg-CDs has been successfully used to the determination of DA in human serum with high accuracy and satisfactory recovery.

MnO2 nanosheets based catechol oxidase mimics for robust electrochemical sensor: Synthesis, mechanism and its application for ultrasensitive and selective detection of dopamine

Nanozymes have favorable activity and good stability, which are potential alternatives to natural enzymes and widely applied in biosensing. However, nanozymes based electrochemical sensors are fewer, because many nanozymes are not easy to form efficient electrocatalytic interface and experience interference from the possible oxidizable species. Herein, ultrathin MnO2 nanosheets (MnO2 NSs) were synthesized by reduction of KMnO4 in acidic environment by chemical precipitation method. The MnO2 NSs show excellent catechol oxidase mimicking activity. The steady-state kinetics of MnO2 NSs shows a higher Vmax of 3.441 µM s−1. Additionally, the catalytic mechanism is that in the presence of oxygen, catechol or its analogues are oxidized to quinone or quinoids, while oxygen is reduced to H2O. Afterwards, the possible mechanism of dopamine (DA) at MnO2 NSs-modified electrode is investigated. DA is first catalytically oxidized to dopamine quinone (DQ) by MnO2 NSs based catechol oxidase, which further undergoes irreversible electrochemical reduction to DA involving two protons and two electrons transfer during the process. On the basis of this, a selective and ultrasensitive amperometric detection of DA at 0.0 V (vs. SCE) was explored, which have two linear parts, 0.01–20 μM and 20–100 μM DA with the LOD of 4.1 nM (S/N = 3). Most importantly, the presence of oxidizable species including ascorbic acid, uric acid and cysteine may coexist with DA in biological systems do not exhibit any appreciable interference. The as-proposed method was applicable to detect DA in human serum samples with good satisfactory accuracy and recovery. This research casts prospect to apply nanozymes for electrochemical sensor with excellent analytical performance.

Tailored multi-layer graphene arrays for precision detection of neurotransmitter

The development of sensitive dopamine (DA) sensors has significantly contributed to our understanding of DA-related disorders and has enabled advancements in medical diagnostics and neuroscience research. Therefore, in the present work, a novel electrochemical sensing platform was developed using multi-layer graphene arrays (MGA) modified electrodes for the selective detection of DA. The preparation of high-quality MGA was achieved using the plasma-enhanced chemical vapor deposition (PCVD) method and was confirmed using various physiochemical techniques such as transmission electron microscopy and Raman spectroscopy. The modified electrode, made of MGA, was utilized for the electrochemical detection of DA using cyclic voltammetry and amperometry i-t methods. DA’s electrochemical oxidation response and sensitivity at the MGA electrode were ≈9 and 3 times higher than observed with unmodified and commercially available multi-layer graphene-modified electrodes. The MGA sensor exhibited excellent analytical parameters for DA detection, including a wide linear range of up to 172.1 μM and a low detection limit of 1.3 nM. The sensor also demonstrated remarkable sensitivity, storage stability, and selectivity for DA detection, making it highly suitable for accurately detecting DA in medical diagnostics and neuroscience research. Furthermore, the practical application of the MGA sensor for DA detection was demonstrated in various real samples.

Ultrafast and selective detection of dopamine by DC sputtered highly oriented CuO thin films: Effect of electroactive interfering agents and temperature

Dopamine and serotonin are two neurotransmitters that play critical role in human physiology. In this work, it has been aimed to synthesize a chip-based sensing platform that can detect dopamine precisely in a non-enzymatic way in presence of a series of electroactive interfering agents. Copper oxide (CuO), a p-type material with excellent surface and electrochemical properties, has been deposited through direct current (DC) sputtering technique on indium doped tin oxide (ITO) coated glass substrates as the sensing platform. The structure, phase purity and other essential properties of the modified electrode were established through x-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), Fourier transform infrared spectroscopy (FTIR) and ultraviolet – visible (UV–Vis) spectroscopy. Detailed electrochemical investigations with the modified electrode have also been carried out using cyclic voltammetry (CV), chronoamperometry (i – t) and electrochemical impedance spectroscopy (EIS) that revealed ultrafast response (10 ms), excellent sensitivity (5.41 µAµM-1cm−2) and low limit of detection (LoD) of 0.46 µM for the electrode towards dopamine. The electrode exhibited sensitivity of 0.37 µAµM-1cm−2 with average LoD of 19.2 µM towards serotonin, which is inferior to dopamine. The threshold response potential was also quite different for dopamine and serotonin. The modified electrode was also found to be nonresponsive to a series of electroactive interfering agents, making it dopamine selective. The role of p-type conductivity of the electrode material towards such selective detection of dopamine was also explained. The electrode was notably reliable from the point of view of electrochemical performance and structural stability. Real sample analysis was also carried out by taking urine sample from adult male human.

Hydrogel/MOF Dual-Modified Photoelectrochemical Biosensor for Antibiofouling and Biocompatible Dopamine Detection.

For accurate in vivo detection, nonspecific adsorption of biomacromolecules such as proteins and cells is a severe issue. The adsorption leads to electrode passivation, significantly compromising both the sensitivity and precision of sensing. Meanwhile, common antibiofouling modifications, such as polymer coatings, still grapple with issues related to biocompatibility, electrode passivation, and miniaturization. Herein, we propose a composite antibiofouling coating strategy based on zwitterionic metal-organic frameworks (Z-MOFs) and a combination of acrylamide hydrogels. On a well-designed TiO2/Z-MOF/hydrogel photoelectrode, we achieve highly sensitive and selective detection of dopamine in complex biological environments. The hydrogel's three-dimensional porous structure combined with unique microporous architecture of Z-MOF ensures effective sieving of interfering macromolecules while preserving efficient small molecules and electron transport. This innovative approach paves the way for constructing miniature, in vivo antibiofouling sensors for molecule monitoring in living organisms with complicated chemical environments.

Reliable ratiometric colorimetric monitoring of dopamine in practice based on the catalytic signal amplification of nano CeO2/CuO modified carboxylated chitosan

To reliably monitor dopamine (DA), a common neurotransmitter, a kind of nano CeO2/CuO modified carboxylated chitosan nanozyme (CeO2/CuO@CC) was constructed under microwave-assisted conditions. The proposed CeO2/CuO@CC exhibited superior synergistic- enhancement oxidase-like activity, with high specific surface area and superior stability. It could accelerate the oxidization of colorless 3,3′,5,5′-tetramethylbenzidine (TMB) into blue oxTMB in the air. What’s more, the presence of trace DA could exclusively change the enzyme-like activity of CeO2/CuO@CC, accompanied with visual color changes from blue to colorless. Under the optimized conditions, there expressed double ratiometric linear relationships between lg(A652/A285)/lg(A370/A285) and cDA, with a large linear range between 6.0 × 10−9 and 1.0 × 10−5 M of DA. When applied for visual detection of DA in real samples, the detection limit was low to 2.0 × 10−9 M with RSD % less than 4.14 %. The mechanisms for enhanced oxidase-mimic activity of CeO2/CuO@CC and its selective detection of DA were proposed. This work will offer an insight to design efficient nanozyme for visual detection of bio-analytes in practice.

Graphene Nanocomposite Ink Coated Laser Transformed Flexible Electrodes for Selective Dopamine Detection and Immunosensing.

Novel and flexible disposable laser-induced graphene (LIG) sensors modified with graphene conductive inks have been developed for dopamine and interleukin-6 (IL-6) detection. The LIG sensors exhibit high reproducibility (relative standard deviation, RSD = 0.76%, N = 5) and stability (RSD = 4.39%, N = 15) after multiple bendings, making the sensors ideal for wearable and stretchable bioelectronics applications. We have developed electrode coatings based on graphene conductive inks, poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (G-PEDOT:PSS) and polyaniline (G-PANI), for working electrode modification to improve the sensitivity and limit of detection (LOD). The selectivity of LIG sensors modified with the G-PANI ink is 41.47 times higher than that of the screen-printed electrode with the G-PANI ink modification. We have compared our fabricated bare laser-engraved Kapton sensor (LIG) with the LIG sensors modified with G-PEDOT (LIG/G-PEDOT) and G-PANI (LIG/G-PANI) conductive inks. We have further compared the performance of the fabricated electrodes with commercially available screen-printed electrodes (SPEs) and screen-printed electrodes modified with G-PEDOT:PSS (SPE/G-PEDOT:PSS) and G-PANI (SPE/G-PANI). SPE/G-PANI has a lower LOD of 0.632 μM compared to SPE/G-PEDOT:PSS (0.867 μM) and SPE/G-PANI (1.974 μM). The lowest LOD of the LIG/G-PANI sensor (0.4084 μM, S/N = 3) suggests that it can be a great alternative to measure dopamine levels in a physiological medium. Additionally, the LIG/G-PANI electrode has excellent LOD (2.6234 pg/mL) to detect IL-6. Also, the sensor is successfully able to detect ascorbic acid (AA), dopamine (DA), and uric acid (UA) in their ternary mixture. The differential pulse voltammetry (DPV) result shows peak potential separation of 229, 294, and 523 mV for AA-DA, DA-UA, and UA-AA, respectively.

ZnO-CeO2 Hollow Nanospheres for Selective Determination of Dopamine and Uric Acid.

ZnO-CeO2 hollow nanospheres have been successfully synthesized via the hard templating method, in which CeO2 is used as the support skeleton to avoid ZnO agglomeration. The synthesized ZnO-CeO2 hollow nanospheres possess a large electrochemically active area and high electron transfer owing to the high specific surface area and synergistic effect of ZnO and CeO2. Due to the above advantages, the resulting ZnO-CeO2 hollow spheres display high sensitivities of 1122.86 μA mM-1 cm-2 and 908.53 μA mM-1 cm-2 under a neutral environment for the selective detection of dopamine and uric acid. The constructed electrochemical sensor shows excellent selectivity, stability and recovery for the selective analysis of dopamine and uric acid in actual samples. This study provides a valuable strategy for the synthesis of ZnO-CeO2 hollow nanospheres via the hard templating method as electrocatalysts for the selective detection of dopamine and uric acid.

Electrochemically selective detection of dopamine over serotonin by CuO/Cu2O bulk heterostructure electrode

Electrochemically selective detection of dopamine over serotonin by CuO/Cu2O bulk heterostructure electrode

Nb4C3Tx MXene-AgNPs decorated laser-induced graphene for selective detection of dopamine

In this study, a selective electrochemical sensor based on Nb4C3Tx MXene-silver nanoparticles (Nb4C3Tx MXene-AgNPs) decorated laser-induced graphene (LIG) electrode synthesized from flexible pyralux film was employed to detect dopamine (DA). The characterization of the synthesized LIG, Nb4C3Tx MXene, and AgNPs was conducted using UV–visible spectroscopy, scanning electron microscopy, and Raman spectroscopy. The electrochemical performance of the fabricated LIG electrode was enhanced from a peak anodic current (Ipa) of 150 μA to 330.4 μA upon modification with Nb4C3Tx MXene-AgNPs nanocomposite. The LIG- Nb4C3Tx MXene-AgNPs electrode exhibited high electrocatalytic activity toward the oxidation of DA via cyclic voltammetry and chronoamperometry techniques. The current response increased linearly with DA concentration and exhibited a wide linear range from 100 nM to 10 µM with a detection limit of 1 nM. The sensor also exhibited an excellent sensitivity of 160.96 μA/nM cm−2. Furthermore, the fabricated LIG-Nb4C3Tx MXene-AgNPs electrode showed excellent selectivity toward DA detection in the presence of common interfering compounds such as glucose, ascorbic acid, and uric acid and had high reproducibility. The developed LIG-Nb4C3Tx MXene-AgNPs flexible electrode platform is suitable for accurately and reliably detecting DA in the presence of competing analytes.