Determination of Trace Cholinergic Compounds and the Evaluation of Their Relative Receptor Activity with the Use of a Receptor Biosensor and an Ion-Selective Choline Electrode

A comparative assessment of the analytical capabilities of a tensoresistive biosensor based on muscarinic acetylcholine receptors and a potentiometric choline sensor was performed. It was found that the receptor biosensor is promising for the determination of ultratrace amounts of cholinergic agents with a detection limit of 10^–7–10^–10 M. The selectivity of the potentiometric choline sensor is equal to the selectivity of the receptor biosensor; however, the sensitivity of the former is lower by two orders of magnitude. Nevertheless, it can be successfully used for evaluating the relative receptor activity of cholinergic agents.     

Molecularly imprinted polymers (MIPs) combined with nanomaterials as electrochemical sensing applications for environmental pollutants

It is known that environmental pollution, which is the result of human-induced industrial, domestic, and agricultural practices, poses a threat to our planet. The increasing human population caused several problems such as water and air pollution, which have reached levels threatening human health. There are many different hazardous chemical and biological environmental pollutants in soil, air, and wastewater. It is extremely important to evaluate these health risks and detect these pollutants. The use of electrochemical methods for the detection of environmental pollutants comes to the forefront recently with advantages such as sensitivity, fast response, low cost, and practical use by miniaturization. The molecular imprinting technique is a popular method used for substance analysis by creating a cavity specific to the substance to be analyzed with the polymer used. The use of molecularly imprinted polymer in electrochemical methods and its modification with various nanomaterials bring advantages such as high selectivity, robustness, and sensitivity to electrochemical sensors. Here, the sensitive determination of environmental pollutants with different nanomaterial-modified molecularly imprinted polymer-based electrochemical sensors, the use of different polymerization techniques, and nano-sized modification agents in sensors are evaluated by reviewing recent studies in the literature.     

Electrochemical biosensors based on Ti3C2Tx MXene: future perspectives for on-site analysis

MXenes are recently developed two-dimensional layered materials composed of early transition metal carbides and/or nitrides that provide unique characteristics for biosensor applications. This review presents the recent progress made on the usage and applications of MXenes in the field of electrochemical biosensors, including microfluidic biosensors and wearable microfluidic biosensors, and highlights the challenges with possible solutions and future needs. The multilayered configuration and high conductivity make these materials as an immobilization matrix for the biomolecule immobilization with activity retention and to be explored in the fabrication of electrochemical sensors, respectively. First, how the MXene nanocomposite as an electrode modifier affects the sensing performance of the electrochemical biosensors based on enzymes, aptamer/DNA, and immunoassays is well described. Second, recent developments in MXene nanocomposites as wearable biosensing platforms for the biomolecule detection are highlighted. This review pointed out the future concerns and directions for the use of MXene nanocomposites to fabricate advanced electrochemical biosensors with high sensitivity and selectivity. Specifically, possibilities for developing microfluidic electrochemical sensors and wearable electrochemical microfluidic sensors with integrated biomolecule detection are emphasized.     

Progress on sensors based on nanomaterials for rapid detection of heavy metal ions

The heavy metal ions,especially Cd~(2+),Pb~(2+) and Hg~(2+),show extremely hazard to the environment and human being.The measurement of heavy metal ions using sensors is catching more and more attention for its advantages of high sensitivity and selectivity,low-cost,convenience to handle and rapid detection.In recent years,nanomaterials such as gold nanoparticles(NPs),magnetic nanoparticles,graphene and nanocomposite materials are applied in sensors for improving sensitivity and selectivity,making the research on electrochemical(EC) sensors,spectrometric biosensors and colorimetric biosensors become a hot spot in the application to investigate heavy metal ions,in particular,Cd~(2+),Pb~(2+) and Hg~(2+).In this short review,the research of advanced detection of Cd~(2+),Pb~(2+) and Hg~(2+) and its progress based on nanomaterial sensors in recent years is reviewed.     

多肽基金属离子传感器

多肽基金属离子传感器作为一种基于多肽序列而设计的新型传感器,越来越受到研究者的关注.多肽作为一类重要的生物小分子,具有合成方法成熟、简便、成本低,且能够以多齿配位状态与金属离子结合等优点.多肽基传感器对金属离子具有高灵敏性和高选择性,且可以通过调节多肽序列进一步优化.与其他类型传感器相比,多肽基金属离子传感器具有良好的...     

Recent Progress on Highly Selective and Sensitive Electrochemical Aptamer-based Sensors

Highly selective, sensitive, and stable biosensors are essential for the molecular level understanding of many physiological activities and diseases. Electrochemical aptamer-based (E-AB) sensor is an appealing platform for measurement in biological system, attributing to the combined advantages of high selectivity of the aptamer and high sensitivity of electrochemical analysis. This review summarizes the latest development of E-AB sensors, focuses on the modification strategies used in the fabrication of sensors and the sensing strategies for analytes of different sizes in biological system, and then looks forward to the challenges and prospects of the future development of electrochemical aptamer-based sensors.     

Application of graphene for preconcentration and highly sensitive stripping voltammetric analysis of organophosphate pesticide

Electrochemical reduced β-cyclodextrin dispersed graphene (β-CD-graphene) was developed as a sorbent for the preconcentration and electrochemical sensing of methyl parathion (MP), a representative nitroaromatic organophosphate pesticide with good redox activity. Benefited from the ultra-large surface area, large delocalized π-electron system and the superconductivity of β-CD-graphene, large amount of MP could be extracted on β-CD-graphene modified electrode via strong π–π interaction and exhibited fast accumulation and electron transfer rate. Combined with differential pulse voltammetric analysis, the sensor shows ultra-high sensitivity, good selectivity and fast response. The limit of detection of 0.05 ppb is more than 10 times lower than those obtained from other sorbent based sensors. The method may open up a new possibility for the widespread use of electrochemical sensors for monitoring of ultra-trace OPs.     

Electrochemical metal-ion sensor based on a cobalt phthalocyanine complex captured in Nafion® on a glassy carbon electrode

This article describes an electrochemical metal-ion sensor based on a cobalt phthalocyanine (CoPc) complex and determination of its sensor activity for some transition metal ions. Ag⁺ and Hg²⁺, among several transition metal ions, coordinate to the sulfur donors of CoPc and alter the electrochemical responses of CoPc in solution, indicating possible application of the complex as Ag⁺ and Hg²⁺ sensor. For practical application, CoPc was encapsulated into a polymeric cation exchange membrane, Nafion, on a glassy carbon electrode and used as an electrochemical coordination element. This composite electrode was potentiometrically optimized and potentiometrically and amperometrically characterized as transition metal-ion sensors with respect to reproducibility, repeatability, stability, selectivity, linear concentration range, and sensitivity. A µmol?dm^?3 sensitivity of the CoPc-based sensor indicates its possible practical application for the determination of Ag⁺ and Hg⁺² in waste water samples.     

基于不同工作电极的亚硝酸盐电化学传感器

亚硝酸盐是环境和生物循环中不可或缺的一部分,但其浓度超标不仅会污染环境,还会致癌。因此对亚硝酸盐实现高效、快速精密检测具有重要的科学和实际意义。基于电化学传感技术的污染物分析与检测已成为研究热点,尤其工作电极的选用和设计对提升响应速度、灵敏度、检测限及降低成本、简化操作等至关重要而备受研究者广泛关注。本文将以玻碳电极、碳糊电极、金属薄膜、聚合物薄膜及碳布电极为分类,针对亚硝酸盐的检测,详细综述基于不同电极的电化学传感器的研究进展。以期通过构建方法和电催化性能的对比为构建新型传感器提供理论与实际指导。     

Nanomaterials based non-enzymatic electrochemical and optical sensors for the detection of carbendazim: A review

Carbendazim sensors with high sensitivity and selectivity have become imperative for the welfare of the food industry, agriculture, aquaculture, and forestry. The design and development of sensors with high sensitivity and selectivity require deeper insights into the chemistry of nanomaterials. Driven by these needs, we intend to offer a concise discussion of diverse materials and various analytical techniques employed for carbendazim detection. This review focuses on interpreting the performance of well-recognized techniques integrated with keenly engineered nanomaterials, critical discussions on the drawbacks of the available sensors, and subsequent advances in nano-tailored materials. This review also provides constructive ideas for the requirement of maiden electrochemical and optical sensors, as well as existing challenges and future prospects.     

Recent advances in electrochemical sensors for antibiotics and their applications

The abuse of antibiotics will cause an increase of drug-resistant strains and environmental pollution,which in turn will affect human health.Therefore,it is important to develop effective detection techniques to determine the level of antibiotics contamination in various fields.Compared with traditional detection methods,electrochemical sensors have received extensive attention due to their advantages such as high sensitivity,low detection limit,and good selectivity.In this mini review,we summarized the latest developments and new trends in electrochemical sensors for antibiotics.Here,modification methods and materials of electrode are discussed.We also pay more attention to the practical applications of antibiotics electrochemical sensors in different fields.In addition,the existing problems and the future challenges ahead have been proposed.We hope that this review can provide new ideas for the development of electrochemical sensors for antibiotics in the future.     

Evaluation of the inhibition of choline uptake in synaptosomes by capillary electrophoresis with electrochemical detection

A direct method for evaluating choline uptake by the high-affinity choline transport system in synaptosomes was developed using capillary electrophoresis (CE) with electrochemical (EC) detection. On-column EC detection of choline and the internal standard, butyrylcholine, was accomplished with a 25 microm platinum electrode modified with the enzymes, choline oxidase and acetylcholinesterase. Choline uptake was evaluated as a function of choline concentration and a KM value of 1.7 microM was determined. The method was also used to evaluate a new class of redox affinity inhibitors of choline transport. In particular, the effectiveness of 3-[(trimethylammonio)methyl]catechol (TMC) as an inhibitor of choline uptake was examined independently and relative to the inhibition of the well-known inhibitor of choline transport, hemicholinium-3. The IC50 and KI for TMC were determined to be 30 microM and 14 microM, respectively. The combination of the selectivity and sensitivity afforded by CEEC provides a relatively straightforward approach for monitoring choline transport in synaptosomes.     

基于金属有机骨架的非酶葡萄糖电化学传感器

葡萄糖的快速有效检测在维持人体健康、疾病控制与诊断、生物科学和食品科学等方面具有重要意义.基于金属有机骨架(MOFs)的催化活性和比表面积大等特点,MOFs已被成功开发为非酶葡萄糖电化学传感器.本文综述了基于非改性MOFs、纳米金属粒子掺杂MOFs、金属及金属氧化物核@MOFs、碳纳米材料@MOFs、核-壳MOFs在检...     

Highly Sensitive Choline Oxidase Enzyme Inhibition Biosensor for Lead Ions Based on Multiwalled Carbon Nanotube Modified Glassy Carbon Electrodes

The determination of lead ions by inhibition of choline oxidase enzyme has been evaluated for the first time using an amperometric choline biosensor. Choline oxidase (ChOx) was immobilized on a glassy carbon electrode (GCE) modified with multiwalled carbon nanotubes (MWCNT) through cross‐linking with glutaraldehyde. In the presence of ChOx, choline was enzymatically oxidized into betaine at –0.3 V versus Ag/AgCl reference electrode, lead ion inhibition of enzyme activity causing a decrease in the choline oxidation current. The experimental conditions were optimised regarding applied potential, buffer pH, enzyme and substrate concentration and incubation time. Under the best conditions for measurement of the lowest concentrations of lead ions, the ChOx/MWCNT/GCE gave a linear response from 0.1 to 1.0 nM Pb²⁺ and a detection limit of 0.04 nM. The inhibition of ChOx by lead ions was also studied by electrochemical impedance spectroscopy, but had a narrower linear response range and low sensitivity. The inhibition biosensor exhibited high selectivity towards lead ions and was successfully applied to their determination in tap water samples.     

Covalently immobilized choline oxidase and cholinesterases on a methacrylate copolymer for disposable membrane biosensors

Bienzymatic sensors for the determination of esters of choline were prepared by covalent co-immobilization of cholinesterases and choline oxidase on polymer membranes, obtained by radiation-induced copolymerization of 2-hydroxyethyl methacrylate and glycidyl methacrylate at low temperature. Optimization of the covalent attachment of choline oxidase and acetyl-or butyrylcholinesterase to copolymer was explored. The enzyme-modified polymers were applied on platinum electrodes to form amperometric sensors, based on the electrochemical detection of enzymatically developed hydrogen peroxide. Acetyl-, acetylthiobutyryl-, and butyrylthiocholine contents in standard solutions were measured, and linear calibration curves were determined. Temperature and pH effects on the electrochemical response are described.     

Electrochemical non-enzymatic glucose sensors

The electrochemical determination of glucose concentration without using enzyme is one of the dreams that many researchers have been trying to make come true. As new materials have been reported and more knowledge on detailed mechanism of glucose oxidation has been unveiled, the non-enzymatic glucose sensor keeps coming closer to practical applications. Recent reports strongly imply that this progress will be accelerated in ‘nanoera’. This article reviews the history of unraveling the mechanism of direct electrochemical oxidation of glucose and making attempts to develop successful electrochemical glucose sensors. The electrochemical oxidation of glucose molecules involves complex processes of adsorption, electron transfer, and subsequent chemical rearrangement, which are combined with the surface reactions on the metal surfaces. The information about the direct oxidation of glucose on solid-state surfaces as well as new electrode materials will lead us to possible breakthroughs in designing the enzymeless glucose sensing devices that realize innovative and powerful detection. An example of those is to introduce nanoporous platinum as an electrode, on which glucose is oxidized electrochemically with remarkable sensitivity and selectivity. Better model of such glucose sensors is sought by summarizing and revisiting the previous reports on the electrochemistry of glucose itself and new electrode materials.     

Miniaturized electrochemical sensors and their point-of-care applications

Most of the current analytical methods depend largely on laboratory-based analytical techniques that require expensive and bullky equipment,potentially incur costly testing,and involve lengthy detection processes.With increasing requirements for point-of-care testing(POCT),more attention has been paid to miniaturized analytical devices.Miniaturized electrochemical(MEC)sensors,including different material-based MEC sensors(such as DNA-,paper-,and screen electrode-based),have been in strong demand in analytical science due to their easy operation,portability,high sensitivity,as well as their short analysis time.They have been applied for the detection of trace amounts of target through measuring changes in electrochemical signal,such as current,voltage,potential,or impedance,due to the oxidation/reduction of chemical/biological molecules with the help of electrodes and electrochemical units.MEC sensors present great potential for the detection of targets including small organic molecules,metal ions,and biomolecules.In recent years,MEC sensors have been broadly applied to POCT in various fields,including health care,food safety,and environmental monitoring,owing to the excellent advantages of electrochemical(EC)technologies.This review summarized the state-of-the-art advancements on various types of MEC sensors and their applications in POCT.Furthermore,the future perspectives,opportunities,and challenges in this field are also discussed.     

酶放大DNA电化学传感器的研究进展

DNA电化学传感器灵敏度高、选择性好、分析时间短和检测成本低,极大地推动了生物传感器的发展. 结合蛋白质酶、功能核酸酶的催化效率高与特异性好,可提高检测灵敏度和选择性. 本文评述了酶放大DNA电化学传感器的研究进展,并分析现存问题,展望发展趋势.     

A Highly Selective and Sensitive Turn-On Fluorescent Chemosensor Based on Rhodamine 6G for Iron(III)

Recently, more and more rhodamine derivatives have been used as fluorophores to construct sensors due to their excellent spectroscopic properties. A rhodamine-based fluorescent and colorimetric Fe³⁺ chemosensor 3’,6’-bis(ethylamino)-2-acetoxyl-2’,7’-dimethyl-spiro[1H-isoindole-1,9’-[9H]xanthen]-3(2H)-one (RAE) was designed and synthesized. Upon the addition of Fe³⁺, the dramatic enhancement of both fluorescence and absorbance intensity, as well as the color change of the solution, could be observed. The detection limit of RAE for Fe³⁺ was around 7.98 ppb. Common coexistent metal ions showed little or no interference in the detection of Fe³⁺. Moreover, the addition of CN⁻ could quench the fluorescence of the acetonitrile solution of RAE and Fe³⁺, indicating the regeneration of the chemosensor RAE. The robust nature of the sensor was shown by the detection of Fe³⁺ even after repeated rounds of quenching. As iron is a ubiquitous metal in cells and plays vital roles in many biological processes, this chemosensor could be developed to have applications in biological studies.     

Graphene–DNAzyme junctions: a platform for direct metal ion detection with ultrahigh sensitivity

Many metal ions are present in biology and in the human body in trace amounts. Despite numerous efforts, metal sensors with ultrahigh sensitivity (<a few picomolar) are rarely achieved. Here, we describe a platform method that integrates a Cu²⁺-dependent DNAzyme into graphene–molecule junctions and its application for direct detection of paramagnetic Cu²⁺ with femtomolar sensitivity and high selectivity. Since DNAzymes specific for other metal ions can be obtained through in vitro selection, the method demonstrated here can be applied to the detection of a broad range of other metal ions.