A Dopamine Detection Sensor Based on Au-Decorated NiS2 and Its Medical Application.

This article reports a simple hydrothermal method for synthesizing nickel disulfide (NiS2) on the surface of fluorine-doped tin oxide (FTO) glass, followed by the deposition of 5 nm Au nanoparticles on the electrode surface by physical vapor deposition. This process ensures the uniform distribution of Au nanoparticles on the NiS2 surface to enhance its conductivity. Finally, an Au@NiS2-FTO electrochemical biosensor is obtained for the detection of dopamine (DA). The composite material is characterized using transmission electron microscopy (TEM), UV-Vis spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The electrochemical properties of the sensor are investigated using cyclic voltammetry (CV), differential pulse voltammetry (DPV), and time current curves in a 0.1 M PBS solution (pH = 7.3). In the detection of DA, Au@NiS2-FTO exhibits a wide linear detection range (0.1~1000 µM), low detection limit (1 nM), and fast response time (0.1 s). After the addition of interfering substances, such as glucose, L-ascorbic acid, uric acid, CaCl2, NaCl, and KCl, the electrode potential remains relatively unchanged, demonstrating its strong anti-interference capability. It also demonstrates strong sensitivity and reproducibility. The obtained Au@NiS2-FTO provides a simple and easy-to-operate example for constructing nanometer catalysts with enzyme-like properties. These results provide a promising method utilizing Au coating to enhance the conductivity of transition metal sulfides.

Miniaturized Implantable Fluorescence Probes Integrated with Metal-Organic Frameworks for Deep Brain Dopamine Sensing.

Continuously monitoring neurotransmitter dynamics can offer profound insights into neural mechanisms and the etiology of neurological diseases. Here, we present a miniaturized implantable fluorescence probe integrated with metal-organic frameworks (MOFs) for deep brain dopamine sensing. The probe is assembled from physically thinned light-emitting diodes (LEDs) and phototransistors, along with functional surface coatings, resulting in a total thickness of 120 µm. A fluorescent MOF that specifically binds dopamine is introduced, enabling a highly sensitive dopamine measurement with a detection limit of 79.9 nM. A compact wireless circuit weighing only 0.85 g is also developed and interfaced with the probe, which was later applied to continuously monitor real-time dopamine levels during deep brain stimulation in rats, providing critical information on neurotransmitter dynamics. Cytotoxicity tests and immunofluorescence analysis further suggest a favorable biocompatibility of the probe for implantable applications. This work presents fundamental principles and techniques for integrating fluorescent MOFs and flexible electronics for brain-computer interfaces and may provide more customized platforms for applications in neuroscience, disease tracing, and smart diagnostics.

Amphetamine-induced reverse transport of dopamine does not require cytosolic Ca2.

Amphetamines (AMPHs) are substrates of the dopamine transporter (DAT) and reverse the direction of dopamine (DA) transport. This has been suggested to depend on activation of Ca2+-dependent pathways, but the mechanism underlying reverse transport via endogenously expressed DAT is still unclear. Here, to enable concurrent visualization by live imaging of extracellular DA dynamics and cytosolic Ca2+ levels, we employ the fluorescent Ca2+ sensor jRGECO1a expressed in cultured dopaminergic neurons together with the fluorescent DA sensor GRABDA1H expressed in cocultured "sniffer" cells. In the presence of the Na+-channel blocker tetrodotoxin to prevent exocytotic DA release, AMPH induced in the cultured neurons a profound dose-dependent efflux of DA that was blocked both by inhibition of DAT with cocaine and by inhibition of the vesicular monoamine transporter-2 with Ro-4-1284 or reserpine. However, the AMPH-induced DA efflux was not accompanied by an increase in cytosolic Ca2+ and was unaffected by blockade of voltage-gated calcium channels or chelation of cytosolic Ca2+. The independence of cytosolic Ca2+ was further supported by activation of N-methyl-D-aspartate-type ionotropic glutamate receptors leading to a marked increase in cytosolic Ca2+ without affecting AMPH-induced DA efflux. Curiously, AMPH elicited spontaneous Ca2+ spikes upon blockade of the D2 receptor, suggesting that AMPH can regulate intracellular Ca2+ in an autoreceptor-dependent manner regardless of the apparent independence of Ca2+ for AMPH-induced efflux. We conclude that AMPH-induced DA efflux in dopaminergic neurons does not require cytosolic Ca2+ but is strictly dependent on the concerted action of AMPH on both vesicular monoamine transporter-2 and DAT.

A Recognition-Molecule-Free Photoelectrochemical Sensor Based on Ti3C2/TiO2 Heterostructure for Monitoring of Dopamine.

Herein, a novel, recognition-molecule-free electrode based on Ti3C2/TiO2 composites was synthesized using Ti3C2 as the Ti source and TiO2 in situ formed by oxidation on the Ti3C2 surface for the selective detection of dopamine (DA). The TiO2 in situ formed by oxidation on the Ti3C2 surface not only increased the catalytically active surface for DA binding but also accelerated the carrier transfer due to the coupling between TiO2 and Ti3C2, resulting in a better photoelectric response than pure TiO2. Through a series of experimental conditions optimization, the photocurrent signals obtained by the MT100 electrode were proportional to the DA concentration from 0.125 to 400 µM, with a detection limit estimated at 0.045 µM. We also monitored DA in human blood serum samples using the MT100 electrode. The results showed good recovery, demonstrating the promising use of the sensor for the analysis of DA in real samples.

Bimetallic Biogenic Pt-Ag Nanoparticle and Their Application for Electrochemical Dopamine Sensor.

In this study, Silver-Platinum (Pt-Ag) bimetallic nanoparticles were synthesized by the biogenic reduction method using plant extracts. This reduction method offers a highly innovative model for obtaining nanostructures using fewer chemicals. According to this method, a structure with an ideal size of 2.31 nm was obtained according to the Transmission Electron Microscopy (TEM) result. The Pt-Ag bimetallic nanoparticles were characterized using Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffractometry (XRD), and Ultraviolet-Visible (UV-VIS) spectroscopy. For the electrochemical activity of the obtained nanoparticles in the dopamine sensor, electrochemical measurements were made with the Cyclic Voltammetry (CV) and Differential Pulse Voltammetry (DPV) methods. According to the results of the CV measurements taken, the limit of detection (LOD) was 0.03 µM and the limit of quantification (LOQ) was 0.11 µM. To investigate the antibacterial properties of the obtained Pt-Ag NPs, their antibacterial effects on Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) bacteria were investigated. In this study, it was observed that Pt-Ag NPs, which were successfully synthesized by biogenic synthesis using plant extract, exhibited high electrocatalytic performance and good antibacterial properties in the determination of dopamine (DA).

Surface-Activated Pencil Graphite Electrode for Dopamine Sensor Applications: A Critical Review.

Pencil graphite electrode (PGE) is an alternative, commercially available, ready-to-use, screen-printed electrode for a wide range of electroanalytical applications. Due to the complex-matrix composition and unpredictable electro-inactive nature of PGE in its native form, a surface pre-treatment/activation procedure is highly preferred for using it as an electroactive working electrode for electroanalytical applications. In this article, we review various surface pre-treatment and modification procedures adopted in the literature with respect to the sensitive and selective detection of dopamine as a model system. Specific generation of the carbon-oxygen functional group, along with partial surface exfoliation of PGE, has been referred to as a key step for the activation. Based on the Scopus® index, the literature collection was searched with the keywords "pencil and dopamine". The obtained data were segregated into three main headings as: (i) electrochemically pre-treated PGE; (ii) polymer-modified PGEs; and (iii) metal and metal nanocomposite-modified PGE. This critical review covers various surface activation procedures adopted for the activation for PGE suitable for dopamine electroanalytical application.

Synthesis and characterization of activated carbon supported bimetallic Pd based nanoparticles and their sensor and antibacterial investigation.

Activated carbon (AC) supported palladium cobalt bimetallic nanoparticles (PdCo@AC NPs) were obtained by green synthesis method using Cinnamomum verum (C. Verum) extract. The obtained NPs were characterized by Fourier Transform Infrared Spectroscopy (FTIR), X-Ray Crystallography (XRD), Transmission Electron Microscope (TEM) and Ultraviolet Visible (UV-VIS) spectroscopy, and the functional groups and morphology of the nanoparticle were elucidated. The resulting particle size was found to be 2.467 nm. NPs were evaluated using Cyclic Voltammetry (CV), Scan Rate (SR), and Differential Pulse Voltammetry (DPV) techniques for potential dopamine sensors application. According to the obtained DPV results, Limit of Detection (LOD) and Limit of Quantitation (LOQ) values are found to be 5.68 pM and 17.21 pM, respectively. It was also observed that AC supported PdCo nanoparticles obtained from C. verum extract sensed dopamine quite well. Besides, to examine the antibacterial properties of NPs, antibacterial analyzes were performed with Escherichia coli (E. Coli) and Staphylococcus aureus (S. Aureus). It was observed that it showed good antibacterial properties against gram positive (S. aureus) and gram negative (E. coli) bacteria. The study gave important results in terms of the synthesis of bimetallic NPs using the green synthesis method and their usability in different areas. With this study, it was observed that a good antibacterial dopamine sensor were obtained with the successful biogenic synthesis of AC supported PdCo bimetallic NPs.

Cyclophosphazene Intrinsically Derived Heteroatom (S, N, P, O)-Doped Carbon Nanoplates for Ultrasensitive Monitoring of Dopamine from Chicken Samples.

A novel, metal-free electrode based on heteroatom (S, N, P, O)-doped carbon nanoplates (SNPO-CPL) modifying lead pencil graphite (LPG) has been synthesized by carbonizing a unique heteroatom (S, N, P, O)-containing novel polymer, poly(cyclcotriphosphazene-co-2,5-dioxy-1,4-dithiane) (PCD), for precise screening of dopamine (DA). The designed electrode, SNPO-CPL-800, with optimized percentage of S, N, P, O doping through the sp2-carbon chain, and a large number of surface defects (thus leading to a maximum exposition number of catalytic active sites) led to fast molecular diffusion through the micro-porous structure and facilitated strong binding interaction with the targeted molecules in the interactive signaling transducer at the electrode-electrolyte interface. The designed SNPO-CPL-800 electrode exhibited a sensitive and selective response towards DA monitoring, with a limit of detection (LOD) of 0.01 nM. We also monitored DA levels in commercially available chicken samples using the SNPO-CPL-800 electrode even in the presence of interfering species, thus proving the effectiveness of the designed electrode for the precise monitoring of DA in real samples. This research shows there is a strong potential for opening new windows for ultrasensitive DA monitoring with metal-free electrodes.

Heterostructured ZnCdS@ZIF-67 as a Photocatalyst for Fluorescent Dye Degradation and Selectively Nonenzymatic Sensing of Dopamine.

Dopamine (DA) plays the role of the transmitter of information in the brain. Neurological diseases and depression are in close relationship with DA release. In this study, we developed a co-catalyst Zn0.2Cd0.8S@zeolitic imidazolate framework-67 (Zn0.2Cd0.8S@ZIF-67) to improve the photocatalyst efficacy of Rhodamine B (RhB) and electrochemical sensing of DA. Results show that Zn0.2Cd0.8S@ZIF-67 exhibits optimal photocatalytic activity with the addition of 80 mg ZIF-67. The degradation percentage of RhB by Zn0.2Cd0.8S@ZIF-67 reached 98.40% when the co-catalyst was 50 mg. Radical trapping experiments show that ·O2- played a significant role in the photocatalytic degradation of RhB. The catalytic mechanism of the Zn0.2Cd0.8S@ZIF-67 was found as a Z-type photocatalysis. Finally, a DA biosensor was constructed and displayed a high response and selectivity to DA. This can be attributed to the heterojunction between Zn0.2Cd0.8S and ZIF-67, which can significantly enhance the separation of e-/h+ and improve charge transfer. These findings will play a positive role in the in-situ monitoring of neurological diseases and depression.

Age-dependent alterations in key components of the nigrostriatal dopaminergic system and distinct motor phenotypes.

The nigrostriatal dopaminergic (DA) system, which includes DA neurons in the ventral and dorsal tiers of the substantia nigra pars compacta (vSNc, dSNc) and DA terminals in the dorsal striatum, is critically implicated in motor control. Accumulating studies demonstrate that both the nigrostriatal DA system and motor function are impaired in aged subjects. However, it is unknown whether dSNc and vSNc DA neurons and striatal DA terminals age in similar patterns, and whether these changes parallel motor deficits. To address this, we performed ex vivo patch-clamp recordings in dSNc and vSNc DA neurons, measured striatal dopamine release, and analyzed motor behaviors in rodents. Spontaneous firing in dSNc and vSNc DA neurons and depolarization-evoked firing in dSNc DA neurons showed inverse V-shaped changes with age. But depolarization-evoked firing in vSNc DA neurons increased with age. In the dorsal striatum, dopamine release declined with age. In locomotor tests, 12-month-old rodents showed hyperactive exploration, relative to 6- and 24-month-old rodents. Additionally, aged rodents showed significant deficits in coordination. Elevating dopamine levels with a dopamine transporter inhibitor improved both locomotion and coordination. Therefore, key components in the nigrostriatal DA system exhibit distinct aging patterns and may contribute to age-related alterations in locomotion and coordination.

Mo and Zn-Dual doped CuxO nanocrystals confined High-Conductive Cu arrays as novel sensitive sensor for neurotransmitter detection.

The development of sensitive and selective sensors using facile and low-cost methods for detecting neurotransmitter molecules is a critical factor in the health care system in regard to early diagnosis. In this research, an electrocatalyst derived from Mo,Zn dual-doped CuxO nanocrystals-based layer coating over one-dimensional copper nanowire arrays (Mo,Zn-CuxO/CuNWs) was successfully designed using a facile electrodeposition approach and used as an electrochemical sensor for non-enzymatic dopamine (DA) neurotransmitter detection. The synergistic effect caused by the dual-doping effect along with its excellent conductivity produced a large electroactive surface area and an improved hetero-charge transfer, thereby boosting DA sensing ability with a low limit detection of 0.32 µM, wide-range of detection (0.5 µM - 3.9 mM), long-term stability (5 weeks), and high selectivity in phosphate buffer solution (pH 7.4). Also, the sensor accurately determined DA in real blood serum-spiked solutions. The achieved results evidenced that the Mo,Zn-CuxO/CuNWs derived sensor is highly suitable for DA detection. Therefore, it also opens new windows for the development of low-cost, accurate, high-performance, and stable sensors for other neurotransmitter sensing for the purposes of better health care and early diagnosis.

An antifouling impedimetric sensor based on zinc oxide embedded polyvinyl alcohol nanoplatelets for wide range dopamine determination in the presence of high concentration ascorbic acid.

Dopamine determination is of great importance for the early diagnosis of neurological diseases. However, dopamine sensors mostly encounter important challenges such as surface fouling and interference of co-existing biochemicals. Here, nanoplatelets of zinc oxide embedded polyvinyl alcohol (NP-ZnO/PVA) were utilized for providing an efficient fouling-free surface for selective dopamine determination in concentrations as high as 3 mM of dopamine in the presence of ascorbic acid interference. The fouling-free properties was provided mainly by pH-inducibility of the NP-ZnO/PVA nanocomposite at the rationally adjusted sensing conditions. ZnO plays a vital role in the electrocatalytic oxidation of dopamine, and PVA provides surface functional groups that minimize the surface interactions with interferences or fouling agents. The NP-ZnO/PVA nanocomposite fabrication process was performed by PVA assisted ZnO electro-synthesis onto the surface of fluorine-doped tin oxide (FTO) conducting glass. The fabricated FTO/NP-ZnO/PVA sensor was characterized utilizing FE-SEM, EDX, XRD, TGA-DTG, BET-BJH and FTIR techniques. Impedimetric determination of dopamine was performed in the wide linear range from 20.0 nM to 3.0 mM with a low detection limit of 5.0 nM. The applicability of FTO/NP-ZnO/PVA for dopamine determination was successfully tested in real samples. The NP-ZnO/PVA provides a great prospective to be an efficacious material for the construction of dopamine electrochemical sensing platforms.

Rationally designed f-MWCNT-coated bismuth molybdate (f-MWCNT@BMO) nanocomposites for the voltammetric detection of biomolecule dopamine in biological samples.

Selective and sensitive dopamine (DPA) sensor was developed using hydrothermally prepared functionalized multi-walled carbon nanotube-coated bismuth molybdate (f-MWCNT@BMO). The f-MWCNT@BMO-reinforced electrode exhibited an outstanding electrocatalytic activity towards DPA oxidation. The nanocomposite-reinforced electrode displayed a rapid response towards DPA sensing and possessed the minimized potential of (Epa + 0.285 V vs Ag/AgCl) in 0.1 M phosphate buffer (PB). The electrochemical results of prepared sensors were analyzed using the differential pulse voltammetry method (DPV). As a result, the f-MWCNT@BMO-reinforced electrode exhibited a widelinear range of 10 nM - 814 µM with a very low detection limit of 3.4 nM towards DPA oxidation. The developed sensor shows excellent selectivity in presence of similar functional group biomolecules. The detection of DPA in real samples was evaluated in human serum, as the results of the proposed sensor possessed good recoveries.

Ventral pallidum DRD3 potentiates a pallido-habenular circuit driving accumbal dopamine release and cocaine seeking.

Drugs of abuse induce persistent remodeling of reward circuit function, a process thought to underlie the emergence of drug craving and relapse to drug use. However, how circuit-specific, drug-induced molecular and cellular plasticity can have distributed effects on the mesolimbic dopamine reward system to facilitate relapse to drug use is not fully elucidated. Here, we demonstrate that dopamine receptor D3 (DRD3)-dependent plasticity in the ventral pallidum (VP) drives potentiation of dopamine release in the nucleus accumbens during relapse to cocaine seeking after abstinence. We show that two distinct VP DRD3+ neuronal populations projecting to either the lateral habenula (LHb) or the ventral tegmental area (VTA) display different patterns of activity during drug seeking following abstinence from cocaine self-administration and that selective suppression of elevated activity or DRD3 signaling in the LHb-projecting population reduces drug seeking. Together, our results uncover how circuit-specific DRD3-mediated plasticity contributes to the process of drug relapse.

The chemical tools for imaging dopamine release.

Dopamine is a modulatory neurotransmitter involved in learning, motor functions, and reward. Many neuropsychiatric disorders, including Parkinson's disease, autism, and schizophrenia, are associated with imbalances or dysfunction in the dopaminergic system. Yet, our understanding of these pervasive public health issues is limited by our ability to effectively image dopamine in humans, which has long been a goal for chemists and neuroscientists. The last two decades have witnessed the development of many molecules used to trace dopamine. We review the small molecules, nanoparticles, and protein sensors used with fluorescent microscopy/photometry, MRI, and PET that shape dopamine research today. None of these tools observe dopamine itself, but instead harness the biology of the dopamine system-its synthetic and metabolic pathways, synaptic vesicle cycle, and receptors-in elegant ways. Their advantages and weaknesses are covered here, along with recent examples and the chemistry and biology that allow them to function.

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.

Boron Doped Carbon Quantum Dots: Turn-Off Fluorescent Probe for Dopamine Detection.

In this report, Boron-doped carbon quantum dots (BCQD, size = 2.3 nm) were fabricated by modified hydrothermal carbonization method by one-pot synthesis using phenyl boronic acid as the common precursor that provided seed for the formation of carbon quantum dots as well as the dopant. These quantum dots exhibited excellent properties including aqueous dispersibility, strong fluorescence emission, good environmental stability, highselectivity and sensitivity towards the neurochemical, dopamine even in the absence of any linker or functionalizing agents. It is shown that this material can be used as a "turn off" fluorescent probe for the detection of even low concentration of dopamine with a minimum detection limit of ~6 µM. The simplicity of synthesis protocol and the easiness of dopamine detection define the novelty of this approach.

N-doped Cu-MOFs for efficient electrochemical determination of dopamine and sulfanilamide.

Fast and efficient tracking of micropollutants in aquatic environment by developing novel electrode materials is of great significance. Herein, a polyvinylpyrrolidone (PVP) assisted strategy is applied for synthesis of nitrogen doped Cu MOFs (N-Cu-MOF) for micropollutants electrochemical detection. The designed N-Cu-MOFs possess uniform octahedral shape with large surface area (1184 m2 g-1) and an average size of roughly 450 nm, exhibiting the excellent electroanalytical capability for the detection of multipollutants. In the case of dopamine (DA) and sulfonamides (SA) as typical microcontaminants, the designed N-Cu-MOFs exhibited wide linear ranges of 0.50 nM-1.78 mM and low detection limit (LOD, 0.15 nM, S/N = 3) for the determination of DA, as well as a linear range of 0.01-58.3 µM and LOD (0.003 µM, S/N = 3) for monitoring SA. The improved performance is attributed to the heteroatom introduction and good dispersion stability of N-Cu-MOF with PVP-decorated. The good electroanalytical ability of N-Cu-MOF for detection of DA and SA can provide a guide to efficient and rapid monitor other micropollutants and construct novel electrochemical sensors.

A feasible sonochemical approach to synthesize CuO@CeO2 nanomaterial and their enhanced non-enzymatic sensor performance towards neurotransmitter.

A nanostructured and high conductive cupric oxide (CuO NPs) with hierarchical CeO2 sheets-like structure was synthesized by a facile sonochemical approach. Furthermore, CuO/CeO2 nanostructure is synthesized by high-intensity ultrasonic probe (Ti-horn, 50 kHz and 100 W) at ambient air. Moreover, the synthesized CuO/CeO2 material was characterized by various analytical techniques including FESEM, EDX, XRD and electrochemical methods. Then, the synthesized CuO/CeO2 composite was applied for the electrocatalytic detection of dopamine using CV and DPV techniques. In addition, the CuO/CeO2 modified electrode has good electrocatalytic performance with high linear range from 0.025 to 98.5 µM towards the determination of dopamine drug and high sensitivity of the CuO/CeO2 modified drug sensor was calculated as 16.34 nM and 4.823 µA·µM-1·cm-2, respectively. Moreover, a repeatability, reproducibility and stability of the CuO@CeO2 mixture modified electrode were analyzed towards the determination of dopamine biomolecule. Interestingly, the real time application of CuO@CeO2 modified electrode was established in different serum and drug samples.

Wearable Fiber-Based Organic Electrochemical Transistors as a Platform for Highly Sensitive Dopamine Monitoring.

Fiber-based organic electrochemical transistors (FECTs) provide a new platform for the realization of an ultrafast and ultrasensitive biosensor, especially for the wearable dopamine (DA)-monitoring device. Here, we presented a fully filament-integrated fabric, it exhibited remarkable mechanical compatibility with the human body, and the minimum sensing unit was an organic electrochemical transistor (OECT) based on PVA- co-PE nanofibers (NFs) and polypyrrole (PPy) nanofiber network. The introduction of NFs notably increased the specific surface area and hydrophilicity of the PA6 filament, resulting in the formation of a large area of intertwined PPy nanofiber network. The electrical performance of PPy nanofiber network-modified fibers improved considerably. For the common FECTs, the typical on/off ratio was up to two orders of magnitude, and the temporal recovery time between on and off states was shortened to 0.34 s. Meanwhile, the device exhibited continuous cycling stability. In addition, the performances of FECT-based dopamine sensors depending on different gate electrodes have also been investigated. The PPy/NFs/PA6 filament-based dopamine sensor was more superior to the gold and platinum (Pt) wires, and the sensor presented long-term sensitivity with a detection region from 1 nM to 1 µM, rapid response time to a set of DA concentrations, remarkable selectivity in the presence of sodium chloride, uric acid, ascorbic acid and glucose, and superior reproducibility. Moreover, it could also be woven into the fabric product. The novel and wearable FECT device shows the potential to become the state-of-the-art DA-monitoring platform.