Facile one-pot method of AuNPs/PEDOT/CNT composites for simultaneous detection of dopamine with a high concentration of ascorbic acid and uric acid

In this research, a facile one-pot method was used to synthesize gold/poly-3,4-ethylene-dioxythiophene/carbon nanotube (AuNPs/PEDOT/CNTs) composite material. The composite material was investigated by Fourier Transform Infrared spectroscopy (FTIR), X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM). Then the synthesized nanocomposite material was dropped on a bare glassy carbon electrode (GCE) to improve the detection performance of dopamine with a high concentration of ascorbic acid and uric acid. The electrochemical behavior of AuNPs/PEDOT/CNTs/GCE was studied by Cyclic Voltammetry (CV), Differential Pulse Voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). Under optimum conditions, AuNPs/PEDOT/CNTs/GCE showed a good linear response in the concentration range from 9.14 to 29.704 μM with a detection limit (LOD) and sensitivity of 0.283 μM and 1.557 μA μM⁻¹, respectively. This sensor was applied to detect practical samples with good average recovery. It also exhibited good reproducibility and stability.

A facile one-pot method was used to synthesize ternary composite material. This modified electrode exhibited good ability of detecting dopamine. It also exhibited excellent anti-interference ability and stability.      

Simultaneous electrochemical determination of levodopa and piroxicam using a glassy carbon electrode modified with a ZnO–Pd/CNT nanocomposite

A highly conductive electrochemical sensor was constructed for the simultaneous electrochemical determination of levodopa and piroxicam by modification of a glassy carbon electrode with a ZnO–Pd/CNT nanocomposite (GCE/ZnO–Pd/CNTs). The ZnO–Pd/CNT nanocomposite was synthesized by the sol–gel procedure and was characterized by EDAX, MAP and SEM. The sensor was shown to improve the oxidation signal of levodopa and piroxicam by ∼70.2-fold and ∼41.5-fold, respectively. This marks the first time that the electrochemical behavior of levodopa and piroxicam have been investigated at the surface of GCE/ZnO–Pd/CNTs. The voltammogram showed a quasi-reversible signal and an irreversible redox signal for electro-oxidation of levodopa and piroxicam, respectively. The GCE/ZnO–Pd/CNTs showed a linear dynamic range of 0.6 to 100.0 μM (at a potential of ∼180 mV) and 0.1 to 90 μM (at a potential of ∼480 mV) with detection limits of 0.08 and 0.04 μM for the determination of levodopa and piroxicam, respectively. GCE/ZnO–Pd/CNTs were then applied for the determination of levodopa and piroxicam in real samples.

A highly conductive electrochemical sensor was constructed for the simultaneous electrochemical determination of levodopa and piroxicam by modification of a glassy carbon electrode with a ZnO–Pd/CNT nanocomposite (GCE/ZnO–Pd/CNTs).     

Ultrathin quasi-hexagonal gold nanostructures for sensing arsenic in tap water

Monodispersed colloidal gold nanoparticles (AuNPs) were synthesized by an easy, cost-effective, and eco-friendly method. The AuNPs were mostly quasi-hexagonal in shape with sizes ranging from 15 to 18 nm. A screen-printed electrode modified with AuNPs (AuNPs/SPE) was used as an electrochemical sensor for the detection of As(iii) in water samples. The mechanistic details for the detection of As(iii) were investigated and an electrochemical reaction mechanism was proposed. Under the optimal experimental conditions, the sensor was highly sensitive to As(iii), with a limit of detection of 0.11 μg L⁻¹ (1.51 nM), which is well below the regulatory limit of 10 μg L⁻¹ established by the United States Environmental Protection Agency and the World Health Organization. The sensor responses were highly stable, reproducible, and linear over the As(iii) concentration range of 0.075 to 30 μg L⁻¹. The presence of co-existing heavy metal cations such as lead, copper, and mercury did not interfere with the sensor response to As(iii). Furthermore, the voltammogram peaks for As(iii), lead, copper, and mercury were sufficiently separate for their potential simultaneous measurement, and at very harsh acidic pH it may be possible to detect As(v). The AuNPs/SPE could detect As(iii) in tap water samples at near-neutral pH, presenting potential possibilities for real-time, practical applications.

Monodispersed colloidal gold nanoparticles (AuNPs) were synthesized by an easy, cost-effective, and eco-friendly method for electrochemical detection of As(iii).     

Synthesis of monodisperse magnetic restricted microspheres for recognition of thiamphenicol in milk

Taking thiamphenicol as the research object, a new type of magnetic restricted access molecularly imprinted polymer (RAM-MMIP) with specific recognition was prepared by a one-step swelling method. The polymer microspheres were characterized and analyzed by scanning electron microscopy, X-ray diffraction, elemental analysis, contact angle measurement and vibrating sample magnetometry. When the ratio of template molecule, functional monomer and cross linking agent was 1 : 4 : 8, the adsorption capacity reached the maximum. Under these conditions, RAM-MIP magnetic solid phase extraction (M-SPE) was combined with HPLC to analyze thiamphenicol in milk samples. Satisfactory linear correlation (R² > 0.9977), good detection limit (LOD: 10.4 μg L⁻¹), high recovery rate (96.5–101.1%), and relative standard deviation (RSD: 2.8–3.8%) were obtained. Therefore, our synthesized material can be used for the analysis of TAP in complex milk samples, and has broad application value.

Taking thiamphenicol as the research object, a new type of magnetic restricted access molecularly imprinted polymer (RAM-MMIP) with specific recognition was prepared by a one-step swelling method.     

Fluorescent sensing platform based on green luminescence carbon dots and AuNPs for clenbuterol detection in pork liver

In this paper, water-soluble green fluorescent carbon dots (G-CDs) were prepared using p-phenylenediamine and glutathione (GSH) as the precursors. The G-CDs exhibit excellent optical properties, and the maximum emission wavelength is located at 522 nm (under 410 nm excitation), which greatly overlaps with the absorption spectrum of AuNPs. Consequently, an effective “off–on” fluorescent sensing platform involved in G-CDs and AuNPs for detection of clenbuterol (CLB) was constructed. The fluorescence of G-CDs was strongly quenched by AuNPs due to the inner filter effect (IFE). As CLB was introduced, the quenched fluorescence intensity was recovered due to the specific interaction between the AuNPs and CLB. The recovered fluorescence intensity is linear to CLB concentration in the range of 13–270 ng mL⁻¹ with a low detection limit of 3.75 ng mL⁻¹. The prepared sensor has been successfully applied for CLB detection in pork liver and could be utilized in food analysis.

Carbon dots (G-CDs) with bright green fluorescence are synthesized by hydrothermal treatment of p-phenylenediamine and glutathione. Employing the G-CDs and AuNPs as sensing platform, a simple fluorescence sensor to detect clenbuterol was established.     

N-Hydroxysuccinimide crosslinked graphene oxide–gold nanoflower modified SPE electrode for sensitive detection of chloramphenicol antibiotic

Here we introduce a composite material that consists of graphene oxide (GO) sheets crosslinked with N-hydroxysuccinimide (NHS) and functionalized with gold nanoflowers (AuNFs). Furthermore, a screen printed electrode (SPE) modified with the introduced composite is electrochemically reduced to obtain an SPE/rGO–NHS–AuNFs electrode for sensitive and selective determination of chloramphenicol (CAP) antibiotic drug. The morphological structure of the as-prepared nanocomposite was characterized by scanning electron microscopy, energy-dispersive X-ray spectroscopy, cyclic voltammetry, Fourier-transform infrared spectroscopy and electrochemical impedance spectroscopy. The proposed sensor demonstrated excellent performance with a linear concentration range of 0.05 to 100 μM and a detection limit of 1 nM. The proposed electrode offers a high level of selectivity, stability, reproducibility and a satisfactory recovery rate for electrochemical detection of CAP in real samples such as blood serum, poultry feed, milk, eggs, honey and powdered milk samples. This further demonstrates the practical feasibility of the proposed sensor in food analysis.

Here we introduce a composite material that consists of graphene oxide (GO) sheets crosslinked with N-hydroxysuccinimide (NHS) and functionalized with gold nanoflowers (AuNFs).     

A dopamine electrochemical sensor based on a platinum–silver graphene nanocomposite modified electrode

A platinum–silver graphene (Pt–Ag/Gr) nanocomposite modified electrode was fabricated for the electrochemical detection of dopamine (DA). Electrochemical studies of the Pt–Ag/Gr nanocomposite towards DA detection were performed by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The CV analysis showed that Pt–Ag/Gr/GCE had enhanced electrocatalytic activity towards DA oxidation due to the synergistic effects between the platinum–silver nanoparticles and graphene. The DPV results showed that the modified sensor demonstrated a linear concentration range between 0.1 and 60 μM with a limit of detection of 0.012 μM. The Pt–Ag/Gr/GCE presented satisfactory results for reproducibility, stability and selectivity. The prepared sensor also showed acceptable recoveries for a real sample study.

A platinum–silver graphene nanocomposite was synthesized and characterized. A nanocomposite modified electrode was fabricated in order to investigate the electrochemical detection of dopamine.     

Switch on fluorescence mode for determination of l-cysteine with carbon quantum dots and Au nanoparticles as a probe

Citric acid and urea were used as precursors for the preparation of carbon quantum dots (CQDs) which exhibited a maximum emission wavelength at 515 nm when excited at 410 nm. Upon addition of citrate-stabilized Au nanoparticles (AuNPs) with the maximum absorption wavelength at 520 nm, the fluorescence of the CQDs could be efficiently quenched, attributed to the energy transfer between CQDs and AuNPs. However, the further introduction of l-cysteine (Cys) could cause the aggregation of AuNPs along with a drop in absorption at 520 nm, resulting in the fluorescence recovery of the CQDs–AuNPs system. Therefore, a simple and reliable switch on fluorescence sensing platform for determination of Cys was constructed. The significant factors, such as pH and incubation time, that affected the detection of Cys were optimized with the AuNP concentration set as 2.50 nM at room temperature. Under the optimized conditions, the fluorescence recoveries (ΔF) were strongly correlated with Cys concentration in the 0.20 to 4.0 μM range, and the detection limit is 0.012 μM. More importantly, our CQD-based sensing platform was successfully used for the detection of Cys in milk samples with high precision and accuracy, indicating the potential of the probe in practical applications.

We demonstrated a fluorescence probe composed of CQDs and AuNPs for switch on detection of Cys, where CQDs as fluorescence reporters and AuNPs as fluorescence quenchers were chosen.     

Green and cost-effective voltammetric assay for spiramycin based on activated glassy carbon electrode and its applications to urine and milk samples

A simple, cost-effective, and efficient differential pulse voltammetric (DPV) assay for monitoring spiramycin adipate (SPA) in its dosage forms, urine, and milk samples at an activated glassy carbon electrode (GCE) was developed. GCE was electrochemically activated by anodization at a high positive voltage (2.5 V). The activated glassy carbon electrode (AGCE) was surface characterized, optimized, and utilized for the electrochemical assay of SPA. The electrochemical behavior of the AGCEs was investigated using cyclic voltammetry (CV) which shows a remarkable increase in the anodic peak of SPA in comparison with GCE. This behavior reflects a remarkable increase in the electrocatalytic oxidation of SPA at AGCE. The impacts of various parameters such as scan rate, accumulation time, and pH were investigated. The analytical performance of the activated glassy carbon electrodes was studied utilizing DPV. Under optimum conditions, the oxidation peak current exhibited two linear ranges of 80 nm to 0.8 μM and 0.85–300 μM with a lower limit of detection (LOD) of 20 nM. The developed assay exhibited high sensitivity, excellent repeatability, and good selectivity. Additionally, the developed SPA-sensitive modified GCE was successfully applied for SPA assay in its pharmaceutical dosage form and diluted biological fluids as well, with satisfactory recovery results which correlated well with the results obtained using spectrophotometry.

An electrochemically activated glassy carbon electrode was utilized as a cost-effective, environmentally friendly, and operationally simple sensor for sensitive and selective determination of spiramycin in dosage form, spiked milk and urine samples.     

Rapid and selective detection of aluminum ion using 1,2,3-triazole-4,5-dicarboxylic acid-functionalized gold nanoparticle-based colorimetric sensor

A highly selective, sensitive, rapid, low-cost, simple and visual colorimetric system for Al³⁺ ion detection was developed based on gold nanoparticles (AuNPs) modified with 1,2,3-triazole-4,5-dicarboxylic acid (TADA). The modified gold nanoparticles (TADA–AuNPs) were first prepared by sodium citrate (Na₃Ct) reduction of chloroauric acid (HAuCl₄) and then capped with a TADA ligand. Five TADA–AuNPs sensors were constructed with sodium citrate (Na₃Ct)/chloroauric acid (HAuCl₄) under different molar ratios. Results showed that the molar ratio of Na₃Ct/HAuCl₄, TADA–AuNPs concentration, pH range and detection time had obvious influences on the performance of this colorimetric method. The optimal detection conditions for Al³⁺ ions were as follows: Na₃Ct/HAuCl4 molar ratio of 6.4 : 1, 0.1 mM of TADA–AuNPs concentration, 4–10 pH range and 90 s of detection time. Under the optimal conditions and using diphenyl carbazone (DPC) as a Cr³⁺ masking agent, this colorimetric sensor exhibited outstanding time efficiency, selectivity and sensitivity for Al³⁺ detection. In particular, the detection limits of this sensor obtained via UV-vis and the naked eye were 15 nM and 1.5 μM, respectively, which were much lower than the current limit (3.7 μM) for drinking water in WHO regulation and better than the previous reports. Moreover, this colorimetric sensing system could be used to for on-site, trace level and real-time rapid detection of Al³⁺ in real water samples.

A colorimetric sensor based on TADA–AuNPs accompanied by a masking agent DPC was constructed, with which the rapid quantification of Al³⁺ can be realized by UV-vis spectroscopy or naked eye observation.     

An electrochemical sensor based on poly(procaterol hydrochloride)/carboxyl multi-walled carbon nanotube for the determination of bromhexine hydrochloride

Poly(procaterol hydrochloride) (p-ProH) polymeric film was successfully deposited onto the carboxyl multi-walled carbon nanotube (CMWCNT) modified glass carbon electrode (GCE) to construct a p-ProH/CMWCNT composite modified GCE. Due to the synergistic effect of p-ProH and CMWCNT in the composite, the developed sensor can enormously enhance the oxidation peak current of bromhexine hydrochloride (BrH) at ca. + 0.90 V. Based on this appearance, an electrochemical method was established for the sensitive and selective determination of BrH with differential pulse voltammetry (DPV). Various conditions affecting the peak current response of BrH were studied and optimized. Under the best conditions, the oxidation peak current of BrH is linear to its concentration in two linear dynamic ranges of 0.2–1.0 μmol L⁻¹ (R = 0.9948) and 1.0–8.0 μmol L⁻¹ (R = 0.9956), with a detection limit of 0.1 μmol L⁻¹ (S/N = 3). Interference experiment indicated that the as-prepared electrochemical sensor showed wonderful selectivity to the recognition of BrH and was free from disturbance of many other electro-active substances such as dopamine, ascorbic and uric acid. Finally, the practicability of the BrH sensor was verified by the satisfactory results acquired from the BrH determination in pharmaceutical preparation and human serum.

The fabrication process of the p-ProH/CMWCNT/GCE.     

Mechanical and thermal properties of carbon nanotubes in carbon nanotube fibers under tension–torsion loading

In carbon nanotube fibers (CNFs) fabricated by spinning methods, it is well-known that the mechanical and thermal performances of CNFs are highly dependent on the mechanical and thermal properties of the inherent CNTs. Furthermore, long CNTs are usually preferred to assemble CNFs because the interaction and entanglement between long CNTs are effectively stronger than between short CNTs. However, in CNFs fabricated using long CNTs, the interior carbon nanotubes (CNTs) inevitably undergo both tension and torsion loading when they are stretched, which would influence the mechanical and thermal performances of CNFs. Here, molecular dynamics (MD) simulations were carried out to study the mechanical and thermal properties of individual CNTs under tension–torsion loading. As for mechanical properties, it was found that both the fracture strength and Young''s modulus of CNTs decreased as the twist angle α increased. Besides, step-wise fracture happened due to stress concentration when the twisted CNTs are stretched. On the other hand, it could be seen that the thermal conductivity of CNTs decreased as α increased. This work presents the systematic investigation of the mechanical and thermal properties of CNTs under tension–torsion loading and provides a theoretical guideline for the design and fabrication of CNFs.

Systematically investigate the mechanical and thermal properties of SWCNT under tension and torsion loadings and provide references for fabricating next-generation super-CNF.     

Oxidised carbon nanotubes as dual-domain synergetic stabilizers in electroconductive carbon nanotube flexible coatings

We report that combining oxidised carbon nanotubes (O-CNTs) and pristine CNTs may be the answer for more electroconductive composites. Short (<1 μm) oxidised multi-wall CNTs (O-MWCNTs) acted as an unobvious and excellent conductivity enhancer in MWCNT-based composite thin films. ‘Blending’ O-MWCNTs (1.5 wt%) with 250 μm-long MWCNTs (98.5 wt%), both of well-defined morphology and physicochemistry, led to a 3- and 26-fold increase in specific conductivity as compared to purely MWCNT- or purely O-MWCNT-based thin films, respectively. We explain the enhanced conductivity by the effect of a dual-domain structure of O-MWCNTs. The scale-up method, i.e. screen-printing, opens a route to application in textronics (i.e. electrical and electronic textiles) and hence targets for medicine, civil/military engineering, wellness, etc.

We report that combining oxidised carbon nanotubes (O-CNTs) and pristine CNTs may be the answer for more electroconductive composites.     

Fabrication of NiO–carbon nanotube/sulfur composites for lithium-sulfur battery application

The practical applications of lithium–sulfur batteries are still a great challenge due to the polysulfide shuttle and capacity decay. Herein, we report a NiO–carbon nanotube/sulfur (NiO–CNT/S) composite by hydrothermal and thermal treatments. This hybrid combines the high conductivity of CNTs and double adsorption of CNTs and NiO (physical and chemical adsorption) to improve the electrochemical performance for the sulfur electrodes. Compared with CNT/S and NiO/S, the developed NiO–CNT/S composites present a preferable initial reversible discharge capacity (1072 mA h g⁻¹) and is maintained at 609 mA h g⁻¹ after 160 cycles at 0.1C.

The NiO–CNT/S composites combine the high conductivity of CNT and double adsorption of CNT and NiO (physical adsorption and chemical adsorption) to enhance electrochemical performance for sulfur electrode materials.     

Homogeneous coating of carbon nanotubes with tailored N-doped carbon layers for improved electrochemical energy storage

The combination of activity-enriched heteroatoms and highly-conductive networks is a powerful strategy to craft carbon-based electrodes for high-efficiency electrochemical energy storage. Herein, N-doped carbon (N-C) coated carbon nanotubes (N-CNTs) were fabricated via a facile in situ synthesis of polyimide in the presence of carbon nanotubes (CNTs), followed by carbonization. The polyimide-divided N-C layers were uniformly covered on the surface of CNTs with a tailored layer thickness. The as-fabricated N-CNTs were further used as electrode active materials for energy storage. When employed as the electrodes for supercapacitors, the N-CNTs exhibited a specific capacitance of 63 F g⁻¹ at 0.1 A g⁻¹ (an energy density of 1.4 W h kg⁻¹ at a power density of 20 W kg⁻¹), which was much higher than that of pure N-C (5 F g⁻¹) and CNTs (13 F g⁻¹). The supercapacitor also retained 66.7% of its initial capacitance (42 F g⁻¹ at 10 A g⁻¹) after a 100-fold increase in the current density and nearly 100% of its initial capacitance after running 10 000 cycles. Furthermore, functioning as an anode material for a Li-ion battery, the N-CNTs also delivered a larger reversible capacity (432 mA h g⁻¹ at 50 mA g⁻¹), higher rate capability, and better cycling stability compared to pure CNTs. The electrochemical performances of the N-CNTs were improved overall due to the synergistic effects of interconnected 3D networks and core–shell structures capable of facilitating electrolyte percolation and charge transportation, enhancing conductivity and surface/interface wettability, and contributing additional pseudocapacitance.

Polyimide-derived N-doped carbon layers were coated onto carbon nanotubes for high-rate electrodes with enhanced energy storage.     

Airflow-assisted dielectrophoresis to reduce the resistance mismatch in carbon nanotube-based temperature sensors

The dielectrophoresis (DEP) method is used to fabricate sensor devices by assembling and aligning carbon nanotubes (CNTs) across electrode structures. The challenges of the method increase as the gap width between the electrodes increases. In this work, a novel DEP setup is proposed to reduce the resistance mismatch in manufacturing carbon nanotube-based sensors. The proposed setup utilizes hot airflow and thermal annealing to fabricate long-aligned multi-walled carbon nanotube (MWCNT) bridges across transparent electrodes with a gap width up to 75 μm. The best alignment results were obtained at airflow velocities between 1.5 m s⁻¹ and 2.5 m s⁻¹. The minimum variation in the resistance of the aligned bridges was 1.81% observed at a MWCNT concentration of 0.005 wt% and deposition time of 10 min. Long MWCNT bridges have many contact points that link MWCNTs to each other, making the contact resistance a robust indicator of the variation in the ambient temperature. The characteristics of the MWCNT bridges as a temperature sensor, including the response, sensitivity, and recovery, were investigated.

Airflow-assisted dielectrophoresis (AA-DEP) is a novel dielectrophoresis (DEP) setup used to fabricate sensor devices with minimum resistance variation by assembling and aligning carbon nanotubes (CNTs) across electrode structures.     

A photoelectrochemical glucose sensor based on gold nanoparticles as a mimic enzyme of glucose oxidase

This work reports the first construction of the ternary layers of ITO/PbS/SiO₂/AuNPs nanostructure for development of photoelectrochemical (PEC) glucose sensor. Herein, the thioglycolic acid-capped PbS quantum dots was employed as a PEC active probe, which is very sensitive to oxygen. The small gold nanoparticles (AuNPs) were act as nanozyme (mimic enzyme of glucose oxidase) to catalytically oxidize glucose in the presence of oxygen, meanwhile consumed oxygen and then resulted in the decrease of cathodic photocurrent. The insertion layer of SiO₂ nanoparticles between PbS and AuNPs could reduce efficiently the base current due to its low electroconductivity, which improved the detection limit. The proposed PEC sensor exhibited high sensitivity and gold selectivity towards glucose. The linear response of glucose concentrations ranged from 1.0 μM to 1.0 mM with detection limit of 0.46 μM (S/N = 3). The results suggest the potential of design and development of numerous nanozyme-based PEC biosensors with the advantage of the simplicity, stability, and efficiency.

This work reports the first construction of the ternary layers of ITO/PbS/SiO₂/AuNPs nanostructure for development of photoelectrochemical (PEC) glucose sensor.     

Direct electrochemical detection of clozapine by RuO2 nanoparticles-modified screen-printed electrode

This study introduces the sensitive electrochemical detection of clozapine with the use of a ruthenium(iv) oxide nanoparticle (RuO₂ NP)-modified screen-printed electrode (RuO₂ NPs/SPE). The electrochemical behaviors of clozapine at RuO₂ NP/SPE have been examined via cyclic voltammetry (CV), differential pulse voltammetry (DPV) and chronoamperometry (CHA). According to the results, the modified electrode has been accompanied by a decreasing over-potential (ca. 170 mV) and enhancement in the peak current (3 times) in comparison with the bare SPE. The results indicated that RuO₂ NP/SPE markedly augmented electro-catalytic activities toward clozapine oxidation. In addition, linear responses have been observed in the range between 0.2 and 500.0 μM with a sensitivity of 0.076 μA μM⁻¹ and a limitation of detection of 0.07 μM (3σ). Moreover, the successful application of RuO₂ NP/SPE has been seen in detecting clozapine in real samples, which showed satisfied recoveries. Therefore, outputs suggest that RuO₂ NP/SPE will be promising for functional utilization.

This study introduces the sensitive electrochemical detection of clozapine with the use of a ruthenium(iv) oxide nanoparticle (RuO₂ NP)-modified screen-printed electrode (RuO₂ NPs/SPE).     

Developing a screen-printed graphite–polyurethane composite electrode modified with gold nanoparticles for the voltammetric determination of dopamine

A screen-printed electrode (SPGPUE) was prepared with graphite–polyurethane composite ink containing gold nanoparticles (AuNPs), resulting in a screen-printed graphite–polyurethane composite electrode modified with gold nanoparticles (SPGPUE–AuNPs). Gold nanoparticles were prepared by the citrate method and extracted from the water medium since polyurethane is not compatible with humidity. After extraction to chloroform, they were characterized via transmission electron microscopy (TEM). The presence of gold on the SPGPUE–AuNP surface was confirmed via SEM and EDX analyses, while thermogravimetry revealed the presence of approximately 3.0% (m/m) gold in the composite. An electrochemical pretreatment in 0.10 mol L⁻¹ phosphate buffer (pH 7.0) with successive cycling between −1.0 V and 1.0 V (vs. pseudo-Ag/AgCl) under a scan rate of 200 mV s⁻¹ and 150 cycles was required in order to provide a suitable electrochemical response for the voltammetric determination of dopamine. After the optimization of the parameters of differential pulse voltammetry (DPV), an analytical curve was obtained within a linear dynamic range of 0.40–60.0 μmol L⁻¹ and detection limit (LOD) of 1.55 ×10⁻⁸ mol L⁻¹ for dopamine at the SPGPUE–AuNP. A non-modified SPGPUE was used for comparison and a linear range was obtained between 2.0 and 10 μmol L⁻¹ with an LOD of 2.94 × 10⁻⁷ mol L⁻¹. During the dopamine determination in cerebrospinal synthetic fluid (CSF), recoveries between 89.3 and 103% were achieved. There were no significant interferences from ascorbic acid and uric acid, but some from epinephrine due to the structural similarity.

A screen-printed modified composite electrode (SPGPUE) was prepared with graphite–polyurethane ink containing gold nanoparticles (AuNPs), resulting in a sensor with improved sensitivity regarding the unmodified device in dopamine determination.     

Robust colorimetric detection based on the anti-aggregation of gold nanoparticles for bromide in rice samples

Inorganic bromide (Br⁻) is an important contaminant ion as it can originate from the overuse of illegal methyl bromide as a fumigant in stored rice samples. Herein, we developed a simple and highly sensitive colorimetric sensor for bromide ion detection in rice samples. The sensor is based on the anti-aggregation of gold nanoparticles (AuNPs) by Br⁻ in the presence of Cr³⁺, which made the method more selective than other typical aggregations of nanoparticles. The AuNPs underwent an aggregation process as a result of the coordination of Cr³⁺ and the carboxylate group of a citrate ion stabilized the AuNPs, resulting in a red-to-blue color change. When Br⁻ was pre-mixed with the AuNPs and Cr³⁺ was added, the solution color changed from blue to red with an increase in the Br⁻ concentration. The anti-aggregation process can be detected with the naked eye and monitored using UV-vis spectrophotometry. The linear calibration curve ranged between 0.31 and 3.75 μM Br⁻ with a low LOD and LOQ of 0.04 and 0.13 μM. The recovery was excellent, ranging from 79.9–92.2% with an RSD of less than 4.0%. The good inter-day and intra-day precisions were 2.9–6.4% and 3.1–7.1%, respectively. The developed sensor has proved to provide a robust method for Br⁻ detection in rice samples.

In this work, we developed a AuNP colorimetric sensor for the facile, sensitive and selective detection of bromide ions in rice samples.