Novel potentiometric sensors for the selective determination of domperidone

The fabrication and electrochemical response characteristics of two novel potentiometric sensors for the selective determination of domperidone (DOM) are described. The two fabricated sensors incorporate DOM–PTA (phosphotungstic acid) ion pair as the electroactive material. The sensors include a PVC membrane sensor and a carbon paste sensor. The sensors showed a linear, stable, and near Nernstian slope of 56.5 and 57.8 mV/decade for PVC membrane and carbon paste sensors, respectively over a relatively wide range of DOM concentration (1.0 × 10^?1–1.0 × 10^?5 and 1.0 × 10^?1–3.55 × 10^?6 M). The response time of DOM–PTA membrane sensor was less than 25 s and that in the case of carbon paste sensor was less than 20 s. A useful pH range of 4–6 was obtained for both types of sensors. A detection limit of 7.36 × 10^?5 M was obtained for PVC membrane sensor and 1.0 × 10^?6 M was obtained for carbon paste sensor. The proposed sensors showed very good selectivity to DOM in the presence of a large number of other interfering ions. The analytical application of the developed sensors in the determination of the drug in pharmaceutical formulations such as tablets was investigated. The results obtained are in good agreement with the values obtained by the standard method. The sensors were also applied for the determination of DOM in real samples such as urine by the standard addition method.     

A New Sensor for Determination of Anionic Surfactants in Detergent Products with Carbon Nanotubes as Solid Contact

A new solid‐state sensor for potentiometric determination of surfactants with a layer of multi‐walled carbon nanotubes was prepared. As a sensing material, 1,3‐didecyl‐2‐methylimidazolium–tetraphenylborate ion‐pair was used. The investigated sensor showed a Nernstian response for both dodecylbenzenesulphonate (DBS, 57.6 mV/decade of activity between 5 × 10^?7 to 1 × 10^?3 M) and sodium lauryl sulfate (LS, 58.4 mV/decade of activity between 2 × 10^?7 to 2 × 10^?3 M). It responded in 8–10 s for each ten‐fold concentration change in the range of 1 × 10^?6 to 3 × 10^?3 M. The detection limits for DS and DBS were 2 × 10^?7 and 3 × 10^?7 M, respectively. The sensor revealed a stable response (signal drift 2.6 mV/h) and exhibited satisfactory selectivity performances for LS over most of the anions generally used in surfactant‐based commercial detergents. The main application of this sensor was the end‐point determination in potentiometric titrations of anionic surfactants. The (diisobutyl phenoxy ethoxy ethyl)dimethyl benzyl ammonium chloride (Hyamine), cetyltrimethylammonium bromide, hexadecylpyridinium chloride monohydrate (HDPC) and 1,3‐didecyl‐2‐methylimidazolium chloride were tested as potential cationic titrants, and all exhibited analytically usable titration curves with well‐defined equivalence points. The standard solution of HDPC was used as a cationic titrant by all potentiometric titrations. The operational life‐time of the sensor described was prolonged to more than 3 months.     

Durable,Sensitive, and Wide‐Range Wearable Pressure Sensors Based on Wavy‐Structured Flexible Conductive Composite Film

Flexible pressure sensors have potential applications in human motion monitoring and electronic skins. To satisfy the practical applications, pressure sensors with a high sensitivity, a low detection limit, a broad response range, and an excellent stability are highly needed. Here, a piezoresistive pressure sensor based on wavy‐structured single‐walled carbon nanotube/graphite flake/thermoplastic polyurethane (SWCNT/GF/TPU) composite film is fabricated by a prestretching process. Due to the random wavy structure, high conductivity, and good flexibility, the prepared sensor displays a low detection limit of 2 Pa, a wide sensing range of 0–60 kPa, and a high sensitivity of 5.49 kPa^?1 for 0–50 Pa. Furthermore, the sensor shows a remarkable repeatability of over 1.1 × 10⁴, 9.0 × 10³, and 2.0 × 10³ pressure loading/unloading cycles at 50 Pa, 500 Pa, and 30 kPa, respectively, and a fast responsibility of 100–150 ms of loading response time and 400–600 ms of relaxation time. Therefore, the pressure sensor is successfully adopted to monitor both the large‐scale human activities (e.g., walk and jump) and the small‐scale signals (e.g., wrist pulse). Furthermore, a sensor array is assembled to map the weight and shape of an object, indicating its various potential applications including human–machine interactions, human health monitoring, and other wearable electronics.     

Synthesis and photophysical behavior of a water‐soluble coumarin‐bearing polymer for proton and Ni2+ ion sensing

BACKGROUND: In recent years, many fluorescent chemosensors with various macromolecular structures have been prepared for the detection of protons or metal cations in the environment. Most of this research is focused on polymer sensors with fluorescent recognition sites in the main chain. In this case, the fluorescent recognition sites are covalently bonded to the polymer chain, and thus the polymer shows photophysical properties as a chemosensor for protons and metal ions. RESULTS: An acrylic monomer bearing coumarin moieties, 7‐hydroxy‐4‐methyl‐8‐(4′‐acryloylpiperazin‐1′‐yl)methylcoumarin, was synthesized. This was then copolymerized with N‐vinylpyrrolidone to obtain a blue fluorescent material. The fluorescent copolymer has good solubility in aqueous solution. Its main photophysical properties were determined in relation to its use as a sensor for protons and metal cations. It is an efficient ‘off‐on’ switcher for pH between 3.02 and 12.08. Additionally, the polymer sensor is selective to Ni²⁺ ions, with the increase in the fluorescence intensity depending on Ni²⁺ ion concentrations in the range 0.33 × 10^?5–7.67 × 10^?5 mol L^?1. CONCLUSION: The results suggest that this copolymer may offer potential as a reusable polymer sensor for protons and Ni²⁺ ions in aqueous solution. Copyright © 2009 Society of Chemical Industry     

A Novel Amperometric Sensor for Salicylic Acid Based on Molecularly Imprinted Polymer-Modified Electrodes

A novel electrochemical MIP-sensor for salicylic acid (SA) has been synthesized firstly by electropolymerizing o-phenylenediamine on glassy carbon electrode in presence of template molecule (salicylic acid). The response of the sensor to SA is investigated by square wave voltammetry (SWV). The linearity is obtained over a concentration range of 6 × 10^?5 ～ 1 × 10^?4 mol/L (R² = 0.9961). And the detection limit of SA is about 2 × 10^?5 mol/L. The sensor exhibits good selectivity for salicylic acid by virtue of the interaction between molecularly imprinted binding sites and the template.     

Determination of Sodium Dodecyl Sulfate in Toothpastes by a PVC Matrix Membrane Sensor

The construction and characteristic performance of a new potentiometric PVC membrane sensor responsive for sodium dodecyl sulfate (SDS) are described. The sensor is based on the use of cetyltrimethylammonium‐tetraphenylborate (CTA‐TPB) ion‐pair complex as electroactive material in PVC matrix in presence of dioctyl phthalate as a solvent mediator. The sensor exhibits a rapid, stable and near‐Nernstian response for SDS over the concentration range of 5 × 10^?3–5 × 10^?6 mol dm^?3 at 25 ± 2 °C and the pH range 4–8.5 with slope of 59.6 mV/decade change in SDS concentration. The lower detection limit is 5 × 10^?6 mol dm^?3 and the response time is 45 s. The determination of selectivity coefficients for different anions shows there is no interference except that of dodecyl benzene sulfonate (DBS^?) ion which has a strong interference. The results obtained in the determination of SDS in toothpastes, using this sensor as an indicator electrode, were compared with those obtained from the spectrophotometric method using methylene blue as the reagent.     

DNA Antenna Tile‐Associated Deoxyribozyme Sensor with Improved Sensitivity

Some natural enzymes increase the rate of diffusion‐limited reactions by facilitating substrate flow to their active sites. Inspired by this natural phenomenon, we developed a strategy for efficient substrate delivery to a deoxyribozyme (DZ) catalytic sensor. This resulted in a three‐ to fourfold increase in sensitivity and up to a ninefold improvement in the detection limit. The reported strategy can be used to enhance catalytic efficiency of diffusion‐limited enzymes and to improve sensitivity of enzyme‐based biosensors.     

Novel Electrochemical Sensor Based on Molecularly Imprinted Polymers with MWCNTs-SiO2 for Selective and Sensitive Detecting 2,4-D

In this study, we introduced molecular imprinting combined with electrochemical method to determine trace 2,4-dichlorophenoxyacetic acid (2,4-D) herbicide in standard solution and actual samples. For this purpose, we synthesis of vinyl silica coated MWCNTs in alkaline environment with surfactant, molecularly imprinted polymers were prepared on the surface of MWCNTs by free radical polymerization, following the composite materials were dissolved in chitosan solution and dropped on the glassy carbon electrode. The functionalized materials were characterized by fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, thermogravimetry and nitrogen adsorption desorption. Electrochemical performance of molecularly imprinted membrane was characterized by cyclic voltammetry, electrochemical impedance spectroscopy and differential pulse voltammetry. Selectivity, stability and reproducibility of the sensors were also studied and discussed. A good linear relationship for supervising 2,4-D from 1.0?×?10^?4 to 1.0?×?10^?8 mol L^?1 with the correlation coefficient of 0.994 and a low LOD of 4.270?nmol?L^?1 (S/N?=?3). The electrochemical sensor has been successfully applied to detect 2,4-D with a recovery rate ranges from 96.2 to 102.4% and a relative standard deviation of less than 4.74%. This work provides potential ideas for detection of trace 2,4-D in real samples.

     

Determination of epigallocatechin‐3‐gallate with a high‐efficiency electrochemical sensor based on a molecularly imprinted poly(o‐phenylenediamine) film

An electrochemical molecularly imprinted polymer (MIP) sensor for detecting the existence of epigallocatechin‐3‐gallate (EGCG) in tea and its products was successfully developed on the basis of a glassy carbon electrode modified with an electropolymerized nonconducting poly(o‐phenylenediamine) film. The properties of the electrode were characterized by cyclic voltammetry, differential pulse voltammetry, and infrared spectroscopy. The template molecules could be rapidly and thoroughly removed by methanol/acetic acid. The linear response range for EGCG was 5.0 × 10^?7–1.0 × 10^?4 mol/L, and the limit of detection was as low as 1.6 × 10^?7 mol/L. The prepared MIP sensor could discriminate between EGCG and its analogs. In addition, satisfactory results were obtained in the detection of real tea samples. The results of our investigation indicate that the MIP sensor was useful for the determination of EGCG with excellent selectivity, high sensitivity, repeatability, and reproducibility. This MIP sensor provides the potential for monitoring the variation of EGCG content during the industrial processes and for predicting the quality of tea and its products. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Synthesis of Manganese Oxide Embedded Carbon Nanofibers as Effective Biomimetic Enzymes for Sensitive Detection of Superoxide Anions Released from Living Cells

Carbon nanofiber/manganese oxide (CNF‐MnO) hybrid nanofibers are synthesized by calcination of potassium permanganate (KMnO₄) loaded bacterial cellulose (BC) hydrogels. The chemical structure, morphology, performance, and application of CNF‐MnO aerogels are characterized and studied. The results revealed that MnO nanoparticles are uniformly deposited on the surface of CNF which derived from BC hydrogels. An amperometric superoxide anions (O₂^??) sensor is fabricated by the immobilization of the CNF‐MnO aerogels on a glassy carbon electrode, which displays a linear amperometric response with a high sensitivity of 76.2 µA cm^?2 × 10^?3m ^?1 and a low detection limit of 1.2 × 10^?9m in the concentration range of 5.0 × 10^?9m – 2.5 × 10^?6m . The successful detection of O₂^?? released from cancer cells verifies the potential application in biomedical field.     

Construction of a novel sensor based on electropolymerization of carmine for voltammetric determination of 4‐nitrophenol

4‐Nitrophenol (4‐NP) has been determined with voltammetric technique based on a novel sensor fabricated by electropolymerization of carmine on a glassy carbon electrode (GCE). An obvious reduction peak located at about ?0.700 V and a couple of redox peaks that were not well‐defined were observed in the potential range of ?1.00 to 0.600 V. Compared with its voltammetric behavior on a bare GCE, the reduction peak potential shifted positively and the peak current increased significantly. All experimental parameters were optimized and linear sweep voltammetry was proposed for its determination. In the optimal conditions, the reduction peak current was proportional to the 4‐NP concentration over the concentration range from 5.00 × 10^?8 to 1.00 × 10^?5 mol L^?1, and the detection limit was 1.00 × 10^?8 mol L^?1 after 200 s of accumulation. The high sensitivity and selectivity of the sensor was demonstrated by its practical application for the determination of trace amounts of 4‐NP in lake water. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3271–3277, 2007     

Selection of RNA-Cleaving TNA Enzymes for Cellular Mg2+ Imaging

Catalytic DNA-based fluorescent sensors have enabled cellular imaging of metal ions such as Mg²⁺. However, natural DNA is prone to nuclease-mediated degradation. Here, we report the in vitro selection of threose nucleic acid enzymes (TNAzymes) with RNA endonuclease activities. One such TNAzyme, T17–22, catalyzes a site-specific RNA cleavage reaction with a k_cat of 0.017 min⁻¹ and K_M of 675 nM. A fluorescent sensor based on T17–22 responds to an increasing concentration of Mg²⁺ with a limit of detection at 0.35 mM. This TNAzyme-based sensor also allows cellular imaging of Mg²⁺. This work presents the first proof-of-concept demonstration of using a TNA catalyst in cellular metal ion imaging.     

Preparation of block copolymers via metal‐free visible‐light‐induced ATRP for the detection of lead ions

Polyacrylamide‐b‐poly(methacrylic acid) was prepared on the surface of Au electrode (Au/PAM/PMAA) for Pb²⁺ ion electrochemical sensing via metal‐free visible‐light‐induced atom transfer radical polymerization, which was very simple, convenient, and environmentally friendly. Au/PAM/PMAA was carefully examined by cyclic voltammetry, electrochemical impedance spectroscopy, and X‐ray photoelectron spectroscopy. Further, Au/PAM/PMAA was successfully used for the determination of Pb²⁺ ion by differential pulse anodic stripping voltammetry. Under the optimal conditions, a linear response from 1.0 × 10^?11 to 1.0 × 10^?4 mol/L with detection limit of 2.5 × 10^?12 mol/L (S/N = 3) was achieved from the results of experiments. Comparing with similar Pb²⁺ sensors, the broader linear range and lower detection limit suggested the promising prospect of Au/PAM/PMAA. In a word, the work of this article had an important significance for the polymer‐modified electrodes and the sensitive detection of Pb²⁺. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45863.     

Zinc ion-imprinted polymer based on silica particles modified carbon paste electrodes for highly selective electrochemical determination of zinc ions

ABSTRACT

In this study, Zn(II) ion-imprinted polymer was prepared on the surface of vinyl silica particles and applied for detection of Zn(II) ions using differential pulse voltametry. The ion- imprinted polymer particles were prepared by free radical polymerization. The prepared particles were characterized by different morphological and elemental techniques. The ion-imprinted particles were used to fabricate the carbon paste electrode as a zinc ions sensor. The modified zinc sensor showed linear response in the concentration range 6.12 × 10^?9 to 4.59 × 10^?8 mol L^?1. The limit of detection and limit of quantification of the electrode were 1.351 × 10^?8 and 4.094 × 10^?8 mol L^?1, respectively.     

A chemiluminescence sensor for determination of epinephrine using graphene oxide–magnetite-molecularly imprinted polymers

A chemiluminescence (CL) sensor for the determination of epinephrine using the system of luminol–NaOH–H₂O₂ based on a graphene oxide–magnetite-molecularly imprinted polymer (GM-MIP) is described. The epinephrine GM-MIP was synthesized using graphene oxide (G) which improved the adsorption capacity, and magnetite nanoparticles which made the polymers easier to use in the sensor. The adsorption performance and properties were characterized. The GM-MIP was used in CL analysis to increase the selectivity and the possible mechanism was also discussed. The CL sensor responded linearly to the concentration of epinephrine over the range 1.04 × 10^?7–7.06 × 10^?3 mol/L with a detection limit of 1.09 × 10^?9 mol/L (3σ). The relative standard deviation for determination was 3.87%. On the basis of speediness and sensitivity, the sensor is reusable and shows a great improvement in selectivity and adsorption capacity over other sensors. The sensor had been used for the determination of epinephrine in drug samples.     

Development of multisensor systems based on chalcogenide thin film chemical sensors for the simultaneous multicomponent analysis of metal ions in complex solutions

A new type of thin film chemical microsensors based on chalcogenide glass-sensitive materials was developed by means of silicon planar technology and pulsed laser deposition technique. These miniaturised ion-selective electrodes (ISEs) exhibit Nernstian responses over five concentration decades with detection limits of 1×10⁻⁷ mol/l towards the primary ions Cu and Pb, and 4×10⁻⁷ and 3×10⁻⁵ mol/l towards Cd and Tl, respectively. The thin film microsensors have been shown to be perspective instruments for the simultaneous multicomponent analysis of complex liquid media based on the principles of an ‘electronic tongue’ device. Incorporating the thin film sensors into a sensor array allowed the multicomponent analysis of heavy metal-ion species (Pb²⁺, Cd²⁺, Zn²⁺ and Fe³⁺). The concentrations of Pb²⁺-, Cd²⁺- and Zn²⁺-ions can be determined simultaneously by direct potentiometric measurements using a sensor array of seven all-solid-state thin film chemical microsensors with an accuracy of 15–30%. The sensor array allows overcoming the problem of an insufficient selectivity of single sensors. The suggested microsystem-compatible fabrication technique favours a further miniaturisation, aimed to a fully integrated electrochemical microsystem.     

Gold nanoparticle ensemble on polydopamine/graphene nanohybrid as a novel electrocatalyst for determination of baicalein

A facile and green approach is used to synthesize polydopamine (PDA) functionalized reduced graphene oxide (RGO) via the self‐polymerization of dopamine (DA) under alkaline conditions. The obtained reduced RGO/PDA composite facilitate Au precursor adsorption. Then Au nanoparticles are reduced and assemble onto the surface of RGO/PDA composite form reduced RGO/PDA/gold (RGO/PDA/Au) nanocatalysts. After that, a sensitive electrochemical sensor for baicalein is fabricated based on RGO/PDA/Au nanocatalysts. In this method, the hydroxyl units of PDA can form hydrogen bonding with the phenolic hydroxyl groups of baicalein, making baicalein easily adsorb on the modified electrode surface to enhance the electrochemical response. The electrochemical mechanism of baicalein on the RGO/PDA/Au nanocatalysts modified GCE is thoroughly investigated by cyclic voltammetry. The fabricated electrochemical sensor show good electrochemical activity for baicalein. The linear range of baicalein is 1 × 10^?8 to 15 × 10^?6 mol L^?1 with the detection limit of 3.1 × 10^?9 mol L^?1. Furthermore, the proposed electrochemical sensor can be used to detect real sample. The results reveal that this method provides a new avenue for electrochemical investigation of baicalein in biochemical, pharmaceutical, and clinical research. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 46720.     

Facile synthesis of graphene/polypyrrole 3D composite for a high‐sensitivity non‐enzymatic dopamine detection

One kind of nanocomposite consisting of graphene and polypyrrole was synthesized via a facile and mild way with the assistant of microwave irradiation. The synthesis route was embedding the polypyrrole into the graphene flakes to form a 3D structure, to achieve larger active surface and higher electro‐catalysis property. Structures and components of the composite were measured by X‐ray diffraction, field emission scanning electron microscopy, and Fourier transform infrared spectroscopy. A stronger electrochemical response of electrode with modified resultant was observed in the electrochemical test. Dopamine sensor based on the composite showed a sensitivity of 363 μA mM ^?1 cm^?2, a linear range of 1 × 10^?4 M to 1 × 10^?3 M , and a detection limit of 2.3 × 10^?6 M (S/N = 3). © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44840.     

Evolution of phase morphology and ‘network‐like’ structure of multiwall carbon nanotubes in binary polymer blends during melt‐mixing

Polyamide6 (PA6)/acrylonitrile butadiene styrene copolymer (ABS) blends with unmodified multiwall carbon nanotubes (MWNTs) were prepared via melt‐blending in a conical twin‐screw micro‐compounder with varying melt‐mixing time. To improve the state of dispersion of MWNTs, non‐covalent organic modifiers for MWNTs have been utilized: sodium salt of 6‐amino hexanoic acid (Na‐AHA) and 1‐pyrene‐carboxaldehyde (PyCHO). PA6/ABS blends with MWNTs have shown a phase morphology transition from ‘matrix‐dispersed droplet’ type to ‘co‐continuous’ type as a function of melt‐mixing time with the exception of 40/60 PA6/ABS blend with PyCHO‐modified MWNTs. Non‐isothermal crystallization studies revealed the heterogeneous nucleating action of MWNTs through the presence of double crystallization exothermic peaks (at ～192^°C and >200^°C) while pure PA6 shows bulk crystallization peak at ～192°C. 40/60 and 60/40 (wt/wt) PA6/ABS blends with 5 wt% unmodified MWNTs exhibited electrical conductivity values of ～3.9 × 10^?11 S/cm and ～4.36 × 10^?6 S/cm, respectively. A significant enhancement in electrical conductivity was observed with Na‐AHA and PyCHO‐modified MWNTs (order of ～10^?6 and ～10^?4 S/cm, respectively). POLYM. ENG. SCI., 55:429–442, 2015. © 2014 Society of Plastics Engineers     

Molecularly imprinted electrochemical sensor for the determination of ampicillin based on a gold nanoparticle and multiwalled carbon nanotube‐coated pt electrode

A novel molecularly imprinted electrochemical sensor was developed for the sensitive and selective determination of ampicillin (AMP). The sensor was prepared on a platinum electrode modified with multiwalled carbon nanotubes (MWCNTs), gold nanoparticles (AuNPs), and a thin film of molecularly imprinted polymers (MIPs). MWCNTs and AuNPs were introduced to enhance the sensor's electronic transmission and sensitivity. The molecularly imprinted polymer (MIP) was synthesized using AMP as the template molecule, methacrylic acid as functional monomer, and ethylene glycol maleic rosinate acrylate (EGMRA) as cross‐linker. The performance of the proposed imprinted sensor was investigated using cyclic voltammetry (CV), differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS). The results showed that the imprinted film displayed a fast and sensitive response to AMP. Under optimal conditions, response peak current had a linear relationship with the concentration of AMP in the range of 1.0 × 10^?8 mol/L to 5.0 × 10^?6 mol/L and a detection limit of 1.0 × 10^?9 mol/L (S/N = 3). This imprinted sensor was used to detect AMP in food samples with recoveries of 91.4–105%. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40613.