μM For Dopamine Research Articles

Air plasma fast-induced defect-enriched carbon cloth for simultaneous electrochemical detection of dopamine and uric acid

Herein, we report a fast (10 min) and simple surface treatment of pure carbon cloth (CC) only by an air plasma. The structural characterizations indicate that the air plasma process brings out higher rugosity, more defects, and increased oxygen-related groups on CC surfaces than Ar- or N2-plasma, which can offer abundant capture sites, large electroactive area, and superhydrophilic interface for analytes. As a result, the air-treated CC (CC−PAir) electrode achieves a pronounced improvement of electrocatalytic activity for the [Fe(CN)6]3-/[Fe(CN)6]4- probe evidenced by increased peak currents, decreased peak-to-peak separation, and the lowered resistance of charge transfer. It is also demonstrated that the self-supported CC−PAir electrode possesses excellent sensing performance toward dopamine (DA) and uric acid (UA). The feasibility of the simultaneous electrochemical detection of DA and UA can be verified by their large peak potential gap (∼112 mV) for differential pulse voltammetry. The chronoamperometric sensor yields wide linear ranges of 0.05–100 μM for DA and 0.5–300 μM for UA. The corresponding detection limits are estimated to be 2.6 and 20.4 nM for DA and UA, respectively. The sensor also displays satisfactory selectivity, stability, and reproducibility. Due to good flexibility, the CC−PAir electrode presents great potential for manufacturing wearable and soft electronics for human health monitoring.

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.

Enhance electrochemical sensing of ascorbic acid and dopamine using V-CuO/GO nanocomposite

The electrochemical detection of Ascorbic acid and dopamine is crucial due to their vital roles in biological processes. Both biomolecules coexist in the human body and have the same oxidation potential, leading to electrode fouling and overlapping of oxidation potential. Accurate detection enables monitoring their levels in biological samples, aiding in disease diagnosis and treatment. This study presents the fast and green synthesis of a highly sensitive and selective electrochemical biosensor for the simultaneous detection of dopamine and ascorbic acid. The change in spherical cluster morphology into nanorods enhances the electrode's electroactive surface area, enhancing sensor sensitivity and selectivity. Electrochemical characterization techniques, including cyclic voltammetry and electrochemical impedance spectroscopy, demonstrated excellent electron transportation and low charge transfer resistance. The sensor exhibited simultaneous detection with a low limit of detection of 8 µM for dopamine and 6.9 µM for ascorbic acid, with a wide linear working range. Additionally, the sensor showed excellent selectivity and repeatability with a vast potential gap at simultaneous detection, making it suitable for clinical and food industry applications.

All-Diamond Boron-Doped Microelectrodes for Neurochemical Sensing with Fast-Scan Cyclic Voltammetry.

Neurochemical sensing with implantable devices has gained remarkable attention over the last few decades. A promising area of this research is the progress of novel electrodes as electrochemical tools for neurotransmitter detection in the brain. The boron-doped diamond (BDD) electrode is one such candidate that previously has been reported for its excellent electrochemical properties, including a wide working potential, superior chemical inertness and mechanical stability, good biocompatibility and resistance to fouling. Meanwhile, limited research has been conducted on the BDD as a microelectrode for neurochemical detection. Our team has developed a freestanding, all diamond microelectrode consisting of a boron-doped polycrystalline diamond core, encapsulated in an insulating polycrystalline diamond shell, with a cleaved planar tip for electrochemical sensing. This all-diamond electrode is advantageous due to its - (1) batch fabrication using wafer technology that eliminates traditional hand fabrication errors and inconsistencies, (2) absence of metal-based wires, or foundations, to improve biocompatibility and flexibility, and (3) sp 3 carbon surface with resistance to biofouling, i.e. adsorption of proteins or unwanted molecules at the electrode surface in a biological environment that impedes overall electrode performance. Here, we provide findings on further in vitro testing and development of the freestanding boron-doped diamond microelectrode (BDDME) for neurotransmitter detection using fast scan cyclic voltammetry (FSCV). In this report, we elaborate on - 1) an updated fabrication scheme and work flow to generate all diamond BDDMEs, 2) slow scan cyclic voltammetry measurements of reference and target analytes to understand basic electrochemical behavior of the electrode, and 3) FSCV characterization of common neurotransmitters, and overall favorability of serotonin (5-HT) detection. The BDDME showed a 2-fold increased FSCV response for 5-HT in comparison to dopamine (DA), with a limit of detection of 0.16 µM for 5-HT and 0.26 µM for DA. These results are intended to expand on the development of the next generation BDDME and guide future in vivo experiments, adding to the growing body of literature on implantable devices for neurochemical sensing.

ZIF-8 nanoparticles densely covered MXene as functionalized platform for electrochemical detection of medical small molecules

The high-performance electrochemical detection relies on sensing material with highly active structure, which requires the development of advanced synthesis technique and the study of its structure-activity mechanism. Herein, the few-layer Ti3C2Tx nanosheets densely coated zeolitic imidazole framework-8 nanoparticles (Ti3C2Tx@ZIF-8) have been successfully prepared as a unique precursor, which combines the structural advantages of two-dimensional Ti3C2Tx and porous ZIF-8 nanoparticles, leading to the vast interior spaces for loading electrocatalytic nanomaterials. For this purpose, Ti3C2Tx@Au nanoparticles-ZnO nanoparticles@N-doped carbon (Ti3C2Tx@AuNPs-ZnO@NC) has been obtained for the simultaneous electrochemical detection of pharmaceutical molecules including dopamine (DA), acetaminophen (AC), and xanthine (XA). The materials characterization and sensing analysis results of Ti3C2Tx@AuNPs-ZnO@NC reveal the structure-activity relationship of Ti3C2Tx, AuNPs and NC resulting in the high-performance behaviors, which can be summed up as stable electrochemical active sites and efficient electron transport channels. First, the abundant anchor points are offered by NC for immobilizing AuNPs, which ensure the electrochemical activity of such material. Second, the close combination of few-layer Ti3C2Tx nanosheets and NC provides an ideal channel for electron transmission along with the electrochemical reaction process. The potential application of Ti3C2Tx@AuNPs-ZnO@NC is displayed to develop the electrochemical medical sensor. The detection limits are 41 nM towards DA, 59 nM towards AC, and 67 nM towards XA. The linear ranges are 3–200 μM for DA, 15–500 μM for AC, and 8–350 μM for XA.

MoSe2 nanosheets-based sensor for electrochemical detection of dopamine, ascorbic acid, and uric acid

There has been a growing interest in the field of transition metal dichalcogenide (TMD) materials and their potential applications in the field of electrochemical sensors. In the present work, molybdenum diselenide (MoSe2), as a typical representative of TMD, was prepared using a facile hydrothermal method and characterized in terms of its morphological and structural properties. Then, the obtained MoSe2 was dispersed in various solvents to investigate its electrocatalytic properties towards dopamine (DA), ascorbic acid (AA), and uric acid (UA). The electrochemical measurements revealed that deionized water is an effective solvent to disperse the MoSe2 and modify electrodes with the MoSe2 for electrochemical applications. Furthermore, the glassy carbon electrode (GCE) modified with the MoSe2, referred as GCE-MoSe2, was used as an electrochemical sensor to simultaneously detect the DA, AA, and UA. The GCE-MoSe2 exhibited wide linear detection with concentration ranges of 1–333 µM for DA, 50–3440 µM for AA, and 5–1146 µM for UA in phosphate buffer solution and low detection limits (LODs) of 0.57 µM, 13.7 µM, and 1.75 µM, respectively. The electrode further displayed good selectivity, reproducibility, and stability. This work provides valuable insights on constructing electrochemical sensing devices with high analytical performance using the important two-dimensional (2D) TMD materials.

Pd nanoparticles supported on Fe3O4 particles grafted with poly(acrylamide) gel brush for simultaneous electrochemical‐sensing of dopamine and paracetamol

AbstractIn the present study, a glassy carbon electrode (GCE) modified with Pd nanoparticles deposited on poly(acrylamide) gel brush‐grafted magnetic particles (Pd/PAAmGB@Fe3O4) with core‐shell structure was fabricated for simultaneous electrochemical detection of dopamine (DA) and paracetamol (PA). Electrochemical performance of Pd/PAAmGB@Fe3O4/GCE was evaluated using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and differential pulse voltammetry (DPV). The fabricated sensor exhibited voltammetric sensing with a satisfactory linear determination range from 0.4–41 μM for DA and from 0.5–95 μM for PA. The limit of detection (LOD) was 0.1 μM for DA and 0.17 μM for PA based on signal to noise ratio of 3. The proposed sensor also had excellent reusability and selectivity, good reproducibility and stability, and satisfactory recovery in biomedical examples. It is believed that metal nanoparticles deposited on polymer gel brush composites may offer promising new horizons for sensor growth.

Optical Fibers Functionalized with Single-Walled Carbon Nanotubes for Flexible Fluorescent Catecholamine Detection.

Despite the blockbuster popularity of drugs that act on catecholamine receptors, catecholamine dynamics in human health and disease remain an incomplete picture. Recent advances in fluorescent sensors have enabled unprecedented access to catecholamine dynamics in preclinical animal models, but the requirements of these technologies limit translational value for clinical diagnostics. Here, we present a flexible and convenient tool for fluorescent catecholamine detection by functionalizing optical fibers with single-walled carbon nanotube (SWNT)-based near-infrared catecholamine sensors (nIRCats), a form factor that has potential for more convenient and less invasive clinical translation. We show that these near-infrared functionalized (nIRF) fibers respond to dopamine in a biologically-relevant concentration range (10nM through 1 μM) with a mean ΔF/F0 of 0.022 through 0.411, with no statistically significant effect on signal magnitude after 16-hour exposure to human blood plasma. We further demonstrate the utility of these fibers in as little as 10 μL volumes of clinically relevant biofluids up to 24 weeks after preparation, with a ΔF/F0 of up to 0.059 through 1.127 for 10 nM through 1 μM dopamine. We also introduce a compact, mobile dual-near-infrared fiber photometry rig and demonstrate its success detecting dopamine with 0.005 ΔF/F0 in acute brain slices with nIRF fibers. Together, this fiber-based tool and photometry rig expand the toolbox of catecholamine detection technologies to a broader range of applications.

Nanoarchitectonics of Fe single-atom catalyst modified with flexible wearable patch for sweat biomarker analysis

In personalized medical diagnostics and health monitoring, the analysis of biomarkers in sweat, such as uric acid (UA) and dopamine (DA), offers valuable insights into metabolic states. This study introduces a flexible wearable patch based on Fe single-atom catalysts (FeSAs) to simultaneously detect UA and DA in sweat for comprehensive health assessment. Our wearable patch demonstrated linear response ranges of 1–800 μM for UA and 1–500 μM for DA, with detection limits of 2.68 μM and 3.76 μM, and sensitivities of 0.015 μA μM−1 cm−2 and 0.0176 μA μM−1 cm−2, respectively. Additionally, we integrated agarose hydrogel into the wearable patches, optimizing sweat collection efficiency at agarose concentrations ranging from 2 % to 3.8 %. This innovation enables effective biomarker enrichment directly from the skin surface. In conclusion, our study presents an innovative FeSAs-based electrocatalyst capable of simultaneous detection of low-concentration UA and DA biomarkers.

Simultaneously determining dopamine, acetaminophen and chlorpromazine with high performance on coordinated functional acupuncture needle electrode

Developing fast and sensitive methods to simultaneously analyze neurotransmitter and drug is of scientific significance for diagnosing and treating neurological diseases. Acupuncture can adjust and balance the blood gas, yin and yang and other physiological states through inserting acupuncture needle into the patient’s body, so as to treat diseases, care health and strengthen body. In this study, the stainless-steel needle was used as electrode matrix for the sensor. Gold nanoparticles (Au NPs), polydopamine (PDA) and multi-wall carbon nanotubes (MWCNTs) were layer-by-layer modified onto the bare acupuncture needle (AN) through green and environment-friendly method, and the new interface showed efficient performance for simultaneous monitoring dopamine (DA), acetaminophen (AC) and chlorpromazine (CPZ). It was interesting that the synergistic interface of MWCNTs, PDA and AuNPs exhibits effect conductivity, and high electrocatalytic activity for three molecules. The sensor optimally exhibits wide linear ranges of 0.08–100 and 100–1000 μM for DA, 0.07–100 and 100–1000 μM for AC, 0.1–100 and 100–450 μM for CPZ, respectively. The low detection limits are 0.015, 0.012, and 0.022 µM correspondingly, which are competitively compared to previous reports. In addition, the sensor exhibits good anti-interference ability in the presence of excessive interference. The sensor can successfully monitor DA, AC and CPZ in human serum and urine with the recovery rates from 97.2 % to 102.6 %. The sensor showed good repeatability, stability, and reproducibility. The simultaneous detection of needlelike sensor should play important roles in biomedicine.

Silver@copper-polyaniline nanotubes: Synthesis, characterization and biosensor analytical study

We introduce silver-copper nanoparticles incorporated into polyaniline (PANI) nanotubes using a straightforward and efficient reduction process. In this regard, PANI nanotubes with amine groups were fabricated through oxidation polymerization, followed by the attachment of Ag and Cu precursors to enable the synthesis of Ag-Cu bimetallic nanoparticles (NPs) on the pre-formed PANI nanotubes with the use of hydrazine as a reducing agent. The structural characterization of the synthesized NPs was investigated by UV–Vis spectrophotometer (UV–Vis), Dark-field emission, (EDX), X-ray diffraction (XRD) and field emission (FESEM), while the electrochemical properties were estimated by (CV) and differential pulse voltammetry (DPV). The findings indicated that the Ag-Cu NPs were present in the nanoscale range, well-dispersed, and attached to the surface of PANI nanotubes. Electrochemical investigations revealed that the Ag-Cu@PANI nanotube electrode demonstrated efficient electrooxidation of dopamine and hydroquinone without any interfering reactions, suggesting its potential use as an electrochemical biosensor for simultaneous detection of dopamine and hydroquinone. The proposed NPs-based biosensor was connected to concurrently identify dopamine and hydroquinone, illustrating moo distinguish Confinements of 0.46 µM for dopamine and 0.23 mM for hydroquinone, separately. Additionally, the manufactured sensor identified on a wide direct run the dopamine (5–25 µM), and hydroquinone (0.5–2.5 mM). Alongside these promising comes about, the Ag-Cu@PANI nanotube actualized great solidness and reproducibility, making it a favorable stage for electrochemical biosensing of dopamine and hydroquinone.

Dopamine, an exogenous quorum sensing signaling molecule or a modulating factor in Pseudomonas aeruginosa?

Pseudomonas aeruginosa is recognized globally as an opportunistic pathogen of considerable concern due to its high virulence and pathogenicity, especially in immunocompromised individuals. While research has identified several endogenous quorum sensing (QS) signaling molecules that enhance the virulence and pathogenicity of P. aeruginosa, investigations on exogenous QS signaling molecules or modulating factors remain limited. This study found that dopamine serves as an exogenous QS signaling molecule or modulating factor of P. aeruginosa PAO1, enhancing the production of virulence factors and biofilms. Compared to the control group, treatment with 40 μM dopamine resulted in a 33.1 % increase in biofilm formation, 68.1 % increase in swimming mobility, 63.1 % increase in swarming mobility, 147.2 % increase in the signaling molecule 3-oxo-C12-HSL, and 50.5 %, 28.5 %, 27.0 %, and 33.2 % increases in the virulence factors alginate, rhamnolipids, protease, and pyocyanin, respectively. This study further explored the mechanism of dopamine regulating the biofilm formation and virulence of P. aeruginosa PAO1 through transcriptome and metabolome. Transcriptomic analysis showed that dopamine promoted the expression of virulence genes psl, alg, lasA, rhlABC, rml, and phz in P. aeruginosa PAO1. Metabolomic analysis revealed changes in the concentrations of tryptophan, pyruvate, ethanolamine, glycine, 3-hydroxybutyric acid, and alizarin. Furthermore, KEGG enrichment analysis of altered genes and metabolites indicated that dopamine enhanced phenylalanine, tyrosine, and tryptophan in P. aeruginosa PAO1. The results of this study will contribute to the development of novel exogenous QS signaling molecules or modulating factors and advance our understanding of the interactions between P. aeruginosa and the host environment.

Fabrication of ternary hybrid composites of Co-MOFs/MoS2/PEDOTs for sensitive detection of dopamine and norepinephrine in biological samples

In this study, a simple and multifunctional application for Co-based organic frameworks (Co-MOFs) with molybdenum disulfide (MoS2) and poly(3,4-ethylenedioxythiophene)-polystyrene sulfonate (PEDOTs:PSS) is presented. The Co-MOFs with MoS2 exhibit excellent peroxidase mimicking and catalytic activities, making them suitable for colorimetric dopamine sensors. From an electrochemical standpoint, fouling-free and selective sensing of dopamine (DA) and norepinephrine (NE) is highly challenging. However, the synergistic effect of morphological tunability of Co-MOFs with hybrid composites of MoS2 and PEDOTs:PSS offers a wide detection concentration range of 2 nM-350 µM for DA and 20 nM-1000 µM for NE, high sensitivity, excellent anti-fouling, facile kinetic rate reaction, and rapid signal response. A high selectivity rate was achieved in the presence of twenty times higher concentrations of a mixture of ascorbic acid, uric acid, and other bio-chemical co-interferents. Interestingly, ultrasensitive detection limits of 0.23 nM and 2.18 nM (S/N = 3) were achieved for DA and NE, enabling the real-time precise detection of cellular concentrations in PC12 living cells, and biological fluid samples with simple dilution pretreatments. Moreover, the sensor demonstrated satisfactory reproducibility and stability. Finally, the morphological and composite activity-based probes can detect neurotransmitter concentrations in real samples beyond the concentration limit, suggesting a potential clinical sensor tool.

Electrochemically Grown Hole-Rich NiO(OH) Thin Films toward Hole-Mediated Very Fast and Selective Enzyme-Free Electrochemical Sensing of Dopamine under Simulated Environment.

This work aimed to develop an enzyme-free semiconductor-assisted electrochemical technique for the selective detection of the neurotransmitter dopamine. In this case, electrochemically grown nickel oxyhydroxide [NiO(OH)] thin films were chosen to fabricate the sensing platform, i.e., the electrodes. Chronoamperometry was used to deposit the films on indium tin oxide (ITO) coated glass substrates. The films were thoroughly characterized to establish their structure, composition, phase purity, and electrochemical attributes. Electrochemical sensing characteristics were investigated by means of cyclic and differential pulse voltammetry, steady-state amperometry, and electrochemical impedance spectroscopy. The effects of several interfering agents like glucose, sodium chloride, methanol, hydrogen peroxide, and paracetamol were also studied on the detection attributes of dopamine. Significantly high value of sensitivity (11.87 μA μM-1 cm-2) was obtained for dopamine sensing that was associated with a limit of detection (LoD) of 0.22 μM of dopamine. However, the sensitivity (2.51 μA μM-1 cm-2) and LoD (1.20 μM) obtained for serotonin were inferior compared to those of dopamine. The performance of the electrode toward dopamine sensing was not compromised either in the presence of only serotonin or a series of other electroactive interfering agents, which makes the electrode very much dopamine selective. The dopamine response time was 200 ms, which is notably fast. Extensive studies on the effect of temperature, pH and scan rate on the detection of dopamine by the developed electrode material have also been carried out. The developed electrodes were also found to be notably stable for dopamine detection with a decay of only 6.6% in oxidation peak current density after the 50th cycle. Real-life application of the developed electrode material was checked with urine samples from adult male humans and yielded encouraging results.

Vapor phase polymerization of PEDOT on ITO/glass surfaces for nonenzymatic detection of dopamine

This study demonstrates the deposition of poly(3,4-ethylenedioxythiophene) (PEDOT) as an electrically conductive polymer on the ITO-coated glass surfaces for the production of a non-enzymatic electrochemical sensor to detect dopamine. For this purpose, thin films of PEDOT were synthesized using vapor phase polymerization (VPP) from the corresponding monomer 3,4-ethylenedioxythiophene, in which iron(III)chloride was used as the oxidant. Films were deposited at different substrate temperatures, where the temperature dependence of doping and conjugation levels were studied using FTIR and XPS analyses. The highest doping and conjugation levels, as well as the highest film thickness (380 nm) was observed for the film deposited at 40 °C, which represented the highest conductivity of 111 S/cm. Significant differences were observed between the electrochemical responses of ITO/glass and PEDOT/ITO electrodes. Amperometric measurements indicated a limit of detection value of 2.02 µM for dopamine using as-synthesized PEDOT/ITO electrode.

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.

Innovative use of shrimp shell powder in carbon paste electrode for the electrochemical detection of dopamine and paracetamol: Valorization, characterization and application

The present study outlines the design of an innovative, cost-effective, and environmentally friendly electrochemical sensor, based on a carbon paste electrode (CPE) modified by shrimp shell waste (SSW). The developed electrode was used to facilitate the electrocatalytic detection of two compounds, namely dopamine (DA) and paracetamol (PAR). The use of SSW as an electrode material is ground breaking. The results have shown that the addition of shrimp shell (SS) in the CPE has led to a significant increase in the active surface area (0.504 cm2) and has improved electron transfer by decreasing the charge transfer resistance (17.45 Ω.cm2) at the electrode/solution interface. The SSW was characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffractometry (XRD), and fourier transform infra-red (FTIR). The results show a fibrous and porous structure with high calcium content and other chemical elements including carbon, oxygen, sulphur, phosphorus and nitrogen. The electrochemical behavior of DA and PAR on the CPE-SS electrode was studied using cyclic voltammetry (CV), chronoamperometry (CA), electrochemical impedance spectroscopy (EIS), and square wave voltammetry (SWV) techniques. Additionally, CPE and CPE-SS electrodes were examined by SEM/EDS and FTIR. The effect of scan rate shows that the electrochemical process is diffusion controlled for DA and PAR. The CPE-SS electrode provide a wide linear range, good selectivity, repeatability, precision (≤5%), and low detection limits 3.6 µM and 5.54 µM for DA and PAR, respectively. In addition, the developed sensor was applied to detect DA and PAR in urine, tap water, and pharmaceutical tablets with apparent recoveries.

Exogenous dopamine mitigates the effects of salinity stress in tomato seedlings by alleviating the oxidative stress and regulating phytohormones

Salt stress is a worldwide major threat to agricultural production. The aim was to investigate the effects of exogenous dopamine (DA) treatments on physiological, morphological and biochemical characteristics of tomato seedlings under salinity stress. Salt stress was created using a 100 mM NaCl solution. Dopamine solutions (0, 50, 100 and 200 µM) were applied with 7-day intervals. Salt stress significantly suppressed plant growth and DA treatments alleviated the negative effects of salt stress on the growth of tomato seedlings. 100 µM DA treatment increased plant and root dry weights, plant stem diameter, plant height and, leaf area by 286.84%, 150.00%, 108.37%, 160.89%, and 158.28%, respectively, compared to the control. Under salinity LRWC, SPAD, chl-a, chl-b, and total chlorophyll contents decreased; membrane permeability (MP), H2O2, MDA, proline and sucrose contents, CAT, POD and SOD activities increased. Under salt stress, when 100 µM DA was applied, LRWC, SPAD, chl-a, chl-b, and total chlorophyll contents of plants increased by 13.64%, 18.62%, 43.08%, 64.90%, and 50.00%, while MP reduced by 21.08% compared to the control. When 200 µM DA was applied under salt stress, H2O2, MDA, proline and sucrose contents, and CAT, POD and SOD activities were reduced by 31.86%, 18.66%, 56.00%, 38.24%, 11.16%, 17.81% and 10.80%, respectively, compared to non-DA-treated plants. Exogenous application of DA increased IAA content, decreased ABA content and increased ratio of K+/Na+ and Ca2+/Na+ under salt stress as well. In conclusion, exogenous dopamine treatments effectively prevent cellular damage in tomato seedlings and improve plant tolerance to salt stress.

Biofouling and performance of boron-doped diamond electrodes for detection of dopamine and serotonin in neuron cultivation media

Boron doped diamond has been considered as a fouling-resistive electrode material for in vitro and in vivo detection of neurotransmitters. In this study, its performance in electrochemical detection of dopamine and serotonin in neuron cultivation media Neurobasal™ before and after cultivation of rat neurons was investigated. For differential pulse voltammetry the limits of detection in neat Neurobasal™ medium of 2 µM and 0.2 µM for dopamine and serotonin, respectively, were achieved on the polished surface, which is comparable with physiological values. On oxidized surface twofold higher values, but increased repeatabilities of the signals were obtained. However, in Neurobasal™ media with peptides-containing supplements necessary for cell cultivation, the voltammograms were notably worse shaped due to biofouling, especially in the medium isolated after neuron growth. In these complex media, the amperometric detection mode at +0.75 V (vs. Ag/AgCl) allowed to detect portion-wise additions of dopamine and serotonin (as low as 1–2 µM), mimicking neurotransmitter release from vesicles despite the lower sensitivity in comparison with neat NeurobasalTM. The results indicate substantial differences in detection on boron doped diamond electrode in the presence and absence of proteins, and the necessity of studies in real media for successful implementation to neuron-electrode interfaces.

Colorimetric Sensor Array for Simultaneous Assay of Catecholamine Neurotransmitters Using Various-Sized Citrate-Capped Gold Nanoparticles

Driven by the need to in situ monitoring of the endogenous substances in biological matrices, a simple, rapid and sensitive optical nanoarray system has been designed for determination and visual discrimination of four important catecholamine neurotransmitters: dopamine (DA), epinephrine (EP), norepinephrine (NE) and levodopa (LD). To fabricate this platform, spherical citrate-capped gold nanoparticles (AuNPs) in the size range of 13–42 nm have been employed as sensing elements. For each catecholamine different responses toward the AuNPs was obtained indicating unique aggregation kinetics. When the sensor array exposed to different catecholamines (CAs), both the color and UV–Vis absorbance spectra changed due to the interaction of analytes and AuNPs, creating a unique fingerprint-like pattern for each analyte which can be visually detected by naked eye. To analyze response profiles, we employed unsupervised chemometric algorithms including hierarchical cluster analysis (HCA) and principal component analysis (PCA) and satisfactory class separations were achieved. Furthermore, the sensitive RGB based color difference patterns were generated providing easily monitored visual output. Based on this sensor array, the set of four catecholamine neurotransmitters have been correctly identified and classified in the spiked real urine samples. The target analytes have been well distinguished at low concentrations of 0.3 − 4 μM DA, 0.8 − 10 μM EP, 0.8 − 8 μM NE, and 0.3 − 10 μM LD using the proposed “chemical nose” strategy. We believe that the established optical sensor array can be potentially employed as an efficient discrimination tool for diagnostic and therapeutic applications in the future.