基于溶胶-凝胶壳聚糖／SiO2杂化材料的安培型葡萄糖生物传感器

近年来，基于溶胶-凝胶技术的有机/无机杂化复合材料由于具有有机物的柔性和易修饰性，以及无机物的刚性和稳定性等，因此有利于保持生物分子的活性和生物传感器的研制．壳聚糖(CS)具有易成膜性和生物相容性，其在生物传感器中的研究已受到重视．本文通过原位溶胶-凝胶(Sol-gel)技术，     

新型碳纳米材料——石墨烯及其衍生物在生物传感器中的应用

纳米生物检测是目前纳米科学、生物化学及诊断技术相结合的新的重要研究方向。石墨烯由于具有优良的电子、光学、热学、化学和机械性质,使其具有构筑探针分子和信号传递并放大的三重作用,成为应用于超灵敏生物传感器的理想材料。快速的电子传递和可多重修饰的化学性质使其能够实现准确而高选择性的生物分子检测。石墨烯及其复合材料越来越多地被应用到生物传感器的制备中。本文综述了近几年石墨烯及其衍生物在生物传感器研究中的进展,包括修饰石墨烯的各种材料、多种生物活性物质在石墨烯表面的直接电子转移和石墨烯在酶传感器、免疫传感器、基因传感器以及一些生物小分子的检测等方面的研究。     

活性粒子吸附对ZnO纳米粒子表面光伏特性的影响

作为一种传统的半导体,氧化锌在压电陶瓷、光电化学、光催化、发光器件以及气体传感器等方面具有广阔的应用前景,特别是氧化锌纳米粒子,由于其比表面积大、表面活性较高和对周围环境的敏感性,使其成为传感器研究领域中最有前途的材料,有关生物氧传感器和激光器的光电功能特性以及其能带结构的研究已有报道,     

基于新型纳米传感材料的DNA生物传感器的应用

DNA是构建纳米技术和生物传感技术新设备的良好构建体。DNA生物传感器由于具有灵敏度高、选择性好等特点,近年来获得了飞速发展。研究发现,金属纳米粒子(MNPs)、碳基纳米材料等一系列纳米材料在传感器设计中提高了电化学DNA传感器的传感性能。本文侧重介绍了场效应晶体管、石墨烯、碳纳米管等新型纳米传感材料,以及基于这些材料的DNA生物传感器的最新进展,最后展望了DNA生物传感器的应用前景。     

磁性纳米粒子在生物传感器中的应用研究进展

磁性纳米粒子是一种新型纳米材料,可应用于各种生物活性物质如蛋白质、DNA等的富集和分离,药物的磁靶向,以及疾病的诊断和治疗等许多领域。由于磁性纳米粒子有着独特的化学和物理性能,已经成功应用到磁控生物传感器、DNA传感器、蛋白质传感器、酶传感器以及其它类型的生物传感器中,并显著提高了生物传感器检测的灵敏度、缩短了生化反应的时间和提高检测的通量,为生物传感器领域开辟了广阔的应用前景。本文概述了磁性纳米粒子在生物传感器中的应用研究进展。     

MicroRNAs电化学生物传感器在乳腺癌检测中的研究进展

MicroRNAs是一类内源性非编码小RNA分子,可调控靶基因的表达。特异性microRNAs的失调在诸如癌症、心血管疾病、免疫疾病、神经退行性疾病和皮肤疾病等的发展过程中起着关键作用,常作为疾病早期诊断和预后的生物标志物。电化学生物传感器由于其灵敏、快速、成本低等优势,已经成为传统microRNAs检测方法的一种很有前途的替代方法。本文综述了基于microRNA电化学生物传感器检测乳腺癌的研究进展,并对其所构建的电化学生物传感器的检测方法进行了分析探讨。     

电化学式生物传感器的近期发展动向

电化学式生物传感器是生物传感器的很重要组成部分。新材料用于生物传感器是其新发展的重要研究方向,它包括PVC膜的替代材料,离子交换聚合物膜,有机导电聚合物和氧化还原聚合物等。各学科的相互渗透,使生物传感器出现新颖的设想和概念,包括氧化还原酶的电子导通,超薄组成膜和化学敏感微电化学装置及离子通道传感器与膦酯膜电极。电子鼻和组电极以及生物传感器的微型化都是生物传感器的新发展动向。     

适配体电化学生物传感器研究进展

由于制备简便、易修饰、稳定性好和结合目标物范围广等特点,基于适配体的生物传感器研究工作一直得到广大科研工作者的关注.本文在阐述适配体基本原理的基础之上,结合近年来电化学适配体生物传感器研究领域的最新研究成果,对电化学技术在适配体生物传感器研究领域中的最新进展作一综述与展望.     

海洋毒素电化学生物传感器

由藻类产生的海洋毒素对人类健康和环境安全构成了较大威胁,对其进行快速准确的检测是减小海洋毒素危害的有效手段之一。电化学生物传感器具有快速简便、灵敏度高、检测限低和成本低等特点,为检测海洋毒素提供了新的技术途径。目前,应用于海洋毒素检测中的电化学生物传感器主要有免疫传感器、酶传感器和DNA传感器等。本文综述了迄今为止国内外海洋毒素电化学生物传感器研究所取得的成果,并对其当前研究存在的问题和未来发展趋势进行探讨和展望。     

组织传感器

本文介绍一种新型生物传感器-组织基膜传感器(Tissue-Based Membrane Sensor),并对其发展,分类,结构、制备和展望进行了综述。由于它较其它生物传感器制备简单,成本低廉,灵敏度高,使用寿命长,在生物医学、食品工业及环境保护等科学技术领域得到了应用。     

Immobilized Fullerene C60‐Enzyme‐Based Electrochemical Glucose Sensor

A mixed‐valence cluster of cobalt(II) hexacyanoferrate and fullerene C60‐enzyme‐based electrochemical glucose sensor was developed. A water insoluble fullerene C60‐glucose oxidase (C60‐GOD) was prepared and applied as an immobilized enzyme on a glassy carbon electrode with cobalt(II) hexacyanoferrate for analysis of glucose. The glucose in 0.1 M KCl/phosphate buffer solution at pH = 6 was measured with an applied electrode potential at 0.0 mV (vs Ag/AgCl reference electrode). The C60‐GOD‐based electrochemical glucose sensor exhibited efficient electro‐catalytic activity toward the liberated hydrogen peroxide and allowed cathodic detection of glucose. The C60‐GOD electrochemical glucose sensor also showed quite good selectivity to glucose with no interference from easily oxidizable biospecies, e.g. uric acid, ascorbic acid, cysteine, tyrosine, acetaminophen and galactose. The current of H₂O₂ reduced by cobalt(II) hexacyanoferrate was found to be proportional to the concentration of glucose in aqueous solutions. The immobilized C60‐GOD enzyme‐based glucose sensor exhibited a good linear response up to 8 mM glucose with a sensitivity of 5.60 × 10² nA/mM and a quite short response time of 5 sec. The C60‐GOD‐based glucose sensor also showed a good sensitivity with a detection limit of 1.6 × 10^‐6 M and a high reproducibility with a relative standard deviation (RSD) of 4.26%. Effects of pH and temperature on the responses of the immobilized C60‐GOD/cobalt(II) hexacyanoferrate‐based electrochemical glucose sensor were also studied and discussed.     

光照纳米银颗粒对葡萄糖生物传感器响应电流的抑制

采用纳米银-壳聚糖复合膜固定葡萄糖氧化酶,构建葡萄糖生物传感器.利用计时电流法对不同光照时间纳米银颗粒组装的酶电极响应电流进行了表征.实验结果表明,光照纳米银颗粒可以抑制葡萄糖生物传感器的响应电流;随着光照时间的延长,纳米银颗粒的抑制作用逐渐增强,当光照时间达到120min时,葡萄糖生物传感器的响应电流最小(-3.953μA/cm2).葡萄糖生物传感器响应电流的抑制可能是由纳米银颗粒表面的Ag+离子浓度及表面性能的变化引起的.     

Study on the United Glucose Oxidase Electrode Constructed by Composite Electrode

A novel type of united glucose oxidase (GOD) electrode was designed. Glucose oxidase and ferrocene (Fc), which was a mediator, were added into the composite electrode that was constructed by graphite powder, acetylene black, and epoxy resin. These three materials in composite electrode kept constant proportion in weight. And the optimum amounts of GOD and Fc among united enzyme electrode were 5% and 2%, respectively. The glucose was detected linearly in the concentration range 0.01–9.0 mM with a 20-s steady-state response time and 36 nA/mM of the sensitivity at 0.15 V applied potential. And electrode fouling problem and the response current from the interferents were avoided. The response current of the united GOD electrode had no obvious deterioration within 80 days when stored at 4°C in a refrigerator. The detecting results of human serum by the united GOD electrode had good consistency with that by standard enzyme method. The maximum deviation between these two detecting values was 5%. It might be used for detecting the blood sugar in clinical assay.     

An Arrayed Micro‐glutamate Sensor Probe Integrated with On‐probe Ag/AgCl Reference and Counter Electrodes

Complete all‐in‐one multi‐arrayed glutamate (Glut) sensors have been constructed on a silicon‐based micromachined probe composed of micro‐platinum (Pt) working electrodes, a micro‐silver/silver chloride (Ag/AgCl) reference electrode (RE), and a micro‐Pt counter electrode (CE). The OCP shift of the electrodeposited Ag/AgCl on‐probe micro‐reference electrode compared with a Ag/AgCl wire is <0.1 mV/h. The composition ratio of Ag, Cl, and Pt on the electrodeposited on‐probe micro‐reference electrode is observed to be 1.00 : 0.48 : 0.02 analyzed by EDS. The miniaturized amperometric Glut biosensors were constructed on working electrode sites (electrode area: ∼8.5×10⁻⁵ cm²) of the microprobe modified with glutamate oxidase (GlutOx) enzyme layers for the selective, fast, and continuous detection of L‐glutamate. The sensor selectivity towards common electroactive interferents has been improved significantly by coating the electrode surface with perm‐selective polymer layers, overoxidized polypyrrole (PPY) and Nafion®. The sensitivity, detection range, and response time of the proposed all‐in‐one Glut biosensors are 204.7±5.8 nA μM⁻¹ cm⁻² (N=5), 4.99–109 μM, and 2.7±0.3 sec, respectively and no interferent signals of AA and DA were observed. The sensor can be reused over 19 times of continuous repetitive operation (total measurement time: ∼4 hours) and the sensor sensitivity can retain up to four weeks of storage.     

Microfabricated glucose biosensor with glucose oxidase entrapped in sol-gel matrix

A microfabricated glucose biosensor based on an amperometeric hydrogen peroxide electrode has been developed. A sol-gel layer with 5 A pore size and 2 mum thickness was used as the glucose oxidase entrapping matrix. The sol-gel matrix formed over the silicon-based sensor has good mechanical and chemical stability, and the ability to entrap a large amount of enzyme. The miniaturized electrode sensing system is composed of platinum as both working and counter electrodes and silver as a reference electrode. Nafion(R) coating was applied as the interference limiting layer. A series of technologies, such as standard photolithography, electron beam evaporation and image reverse lift-off were utilized for mass production allowing 143 electrodes to be produced at the same time. The effect of oxidable interferences was <10% of the background value of the sensor response. Calibration tests of a series of individual sensors manufactured from the same silicon wafer and dip coated in the same conditions, showed a highly reproducible response characteristics (linear range up to 500 mg dl(-1) and mean sensitivity of 0.54+/-0.14 nA mg(-1) dl(-1) (n=10)).     

A Self‐Sampling‐and‐Flow Biosensor for Continuous Monitoring

A self‐sampling‐and‐flow biosensor was fabricated by sandwiching a nitrocellulose strip on the working electrode side of the double‐sided microporous gold electrodes and a wicking pad on the counter electrode side. The double‐sided microporous electrodes were formed by plasma sputtering of gold on a porous nylon substrate. Sample was taken up to the enzyme‐immobilized working electrode by the capillary action of the front nitrocellulose strip dipped into the sample solution, analyzed electrochemically at the enzyme‐immobilized electrode, and diffuses out to the backside wicking pad through the micropores of the electrodes, constituting a complete flow cell device with no mechanical liquid‐transporting device. Biosensor was formed by co‐immobilizing the glucose oxidase and electron transfer mediator (ferrocene acetic acid) on the thioctic acid self‐assembled monolayer‐modified working electrode. A typical response time of the biosensor was about 5 min with the sensitivity of 2.98 nA/mM glucose, providing linear response up to 22.5 mM. To demonstrate the use of self‐sampling‐and‐flow biosensor, the consumption rate of glucose in the presence of yeast was monitored for five days.     

Evaluation of an amperometric glucose biosensor based on a ruthenium complex mediator of low redox potential

An amperometric glucose ring-disk biosensor based on a ruthenium complex mediator of low redox potential was fabricated and evaluated. This thin-layer radial flow microsensor (10 μl) with ring-disk working electrode displayed remarkable amperometric sensitivity. For Ru₃(μ₃-O)(AcO)₆(Py)₃(ClO₄) (Ru-Py), a trinuclear oxo-acetate bridged cluster, a reversible redox curve of low redox potential and narrow potential window (redox potentials were −0.190 and −0.106 V versus Ag/AgCl wire, respectively) was observed, which is comparable to many reported mediators such as ferrocene derivatives and other ruthenium complexes. The glucose and hydrogen peroxide assays were carried out with this complex-modified electrode Ru-Py-HRP-GOx/Nafion. The sensitivity was obtained 24 nA (15.4 mA M⁻¹ cm⁻²) for 10 μM glucose and 126 nA (160 mA M⁻¹ cm⁻²) for 5 μM H₂O₂, respectively with a working potential at 0 V versus Ag/AgCl. Ascorbic acid was studied as interference to the glucose assay. The application of 0 V potential versus Ag/AgCl did not avoid the occurrence of the oxidation of ascorbic acid, however, the pre-coating of ascorbate oxidase on the disk part of the ring-disk working electrode efficiently pre-oxidized the ascorbic acid and hence eliminated its interference on the glucose response. The practical reliability was also evaluated by assaying the dialysate from the prefrontal cortex of Wistar rats.     

A Tubulin‐Based Quantitative Assay for Taxol (Paclitaxel) with Enzyme Channeling Sensing

We report the development and characterization of a biosensor for sensitive and rapid determination of the anticancer agent Taxol (paclitaxel). The sensor is based on the interaction of Taxol with its receptor protein tubulin in conjunction with the separation‐free immunosensor technique of enzyme channeling. The sensor system consisted of a three electrode electrochemical cell containing a graphite carbon electrode modified with glucose oxidase and tubulin as working electrode poised at +40 mV (vs. Ag/AgCl). Addition of Taxol, horseradish peroxidase labeled Taxol, glucose and potassium iodide to the cell generated a cathodic current response that was proportional to the concentration of Taxol in the range of 10 to 1 000 pM.     

Inkjet Printed Multi‐walled Carbon Nanotube Sensor for the Detection of Lead in Drinking Water

Electroanalytical methods can be used for the reliable detection of the toxic heavy metal lead in drinking water samples. Inkjet printed electrodes have potential for the rapid and affordable assessment of drinking water. Researchers have shown the electrochemical sensing applicability of inkjet printed electrodes. In this work, Pb²⁺ was detected using an inkjet printed multi‐walled carbon nanotube (IJP‐MW‐CNT) electrode with silver tracks printed underneath. The silver tracks provide the sensor with the conductivity needed for sensitive measurements. MW‐CNT were dispersed in water using bile salts as a surfactant to prepare the ink. The IJP‐MW‐CNT electrode was used as the working electrode with a platinum wire and Ag/AgCl as auxiliary and reference electrode, respectively. The electrodes performance was optimized in 0.1 M acetate buffer (pH=4.3) and had two linear ranges of 5 to 20 ppb (R²=0.99) with a sensitivity of 38 nA/ppb and 20 to 50 ppb (R²=0.98) with a sensitivity of 15 nA/ppb and a limit of detection (LOD) of 1.0 ppb for Pb²⁺. The analytical applicability of electrode was determined by constructing a calibration curve in an unaltered drinking water sample (i. e.) Cincinnati tap water with two linear ranges of 15 to 40 ppb (R²=0.99) with a sensitivity of 1.5 nA/ppb and 40 to 70 ppb (R²=0.99) with a sensitivity of 3.5 nA/ppb and a LOD of 1.0 ppb for Pb²⁺. Effects of copper and cadmium as potential interferents are reported.     

Electrocatalytic Reduction of H2O2 and Oxygen on the Surface of Thionin Incorporated onto MWCNTs Modified Glassy Carbon Electrode: Application to Glucose Detection

A new H₂O₂ enzymeless sensor has been fabricated by incorporation of thionin onto multiwall carbon nanotubes (MWCNTs) modified glassy carbon electrode. First 50 μL of acetone solution containing dispersed MWCNTs was pipetted onto the surface of GC electrode, then, after solvent evaporations, the MWCNTs modified GC electrode was immersed into an aqueous solution of thionin (electroless deposition) for a short period of time <5–50 s. The adsorbed thin film of thionin was found to facilitate the reduction of hydrogen peroxide in the absence of peroxidase enzyme. Also the modified electrode shows excellent catalytic activity for oxygen reduction at reduced overpotential. The rotating modified electrode shows excellent analytical performance for amperometric determination of hydrogen peroxide, at reduced overpotentials. Typical calibration at ?0.3 V vs. reference electrode, Ag/AgCl/3 M KCl, shows a detection limit of 0.38 μM, a sensitivity of 11.5 nA/μM and a liner range from 20 μM to 3.0 mM of hydrogen peroxide. The glucose biosensor was fabricated by covering a thin film of sol–gel composite containing glucose oxides on the surface of thionin/MWCNTs modified GC electrode. The biosensor can be used successfully for selective detection of glucose based on the decreasing of cathodic peak current of oxygen. The detection limit, sensitivity and liner calibration rang were 1 μM, 18.3 μA/mM and 10 μM–6.0 mM, respectively. In addition biosensor can reach 90% of steady currents in about 3.0 s and interference effect of the electroactive existing species (ascorbic acid–uric acid and acetaminophen) is eliminated. The usefulness of biosensor for direct glucose quantification in human blood serum matrix is also discussed. This sensor can be used as an amperometric detector for monitoring oxidase based biosensors.