纳米铂颗粒在酶生物传感器中的应用研究

采用硼氢化钠作为还原剂制备纳米铂颗粒,并分别用羧甲基纤维素(CMC)、羟丙基纤维素(HPC)、聚丙烯酸(PAA)为保护剂,提高纳米铂溶胶的稳定性。将制备的纳米铂颗粒与聚乙烯醇缩丁醛构成复合固酶膜基质,用溶胶-凝胶法固定葡萄糖氧化酶,构建葡萄糖生物传感器。实验表明,纳米铂颗粒可以大幅度提高固定化酶的催化活性。在葡萄糖浓度为10mmol／L的溶液中,响应电流从318nA／cm^2提高到13657nA／cm^2。探讨纳米颗粒效应在固定化酶中所起的作用,并分析不同条件对酶电极响应灵敏度的影响。     

纳米颗粒对葡萄糖生物传感器性能影响的研究

制备了纳米金颗粒和纳米铜颗粒，分别用以修饰葡萄糖生物传感器，并选用丝网印刷金电极测试研究了纳米颗粒对葡萄糖生物传感器性能的影响。结果表明：纳米铜颗粒不能增强葡萄糖生物传感器的响应电流，并且延长了其响应时间；纳米金颗粒增强了葡萄糖生物传感器的响应电流，缩短了其响应时间，提高了其抗干扰性，但不能拓宽其检测的线性范围，并且响应电流受工作电压的影响较大；随着工作电压的下降，响应电流迅速下降，与未修饰葡萄糖生物传感器响应电流下降趋势一致。     

基于金基纳米粒子修饰的生物传感器研究进展

重点介绍了金铂、金银等合金纳米粒子在修饰过氧化氢生物传感器、免疫生物传感器、葡萄糖生物传感器及DNA生物传感器中的应用.金基合金纳米粒子修饰的生物传感器对降低过电位、促进电子传递、提高检测灵敏度和选择性以及保持生物酶活性具有良好的效果.展望了金基纳米粒子在生物传感器领域应用的发展前景.     

CuO-NSG的制备及其在非酶葡萄糖传感器中的应用

采用氮和硫共掺杂石墨烯(NSG)作为固定CuO纳米颗粒的新型载体材料,并将获得的CuO-NSG作为电催化葡萄糖氧化(EGO)的催化剂应用于非酶葡萄糖传感器,解决EGO催化剂的稀缺性和高成本性。结果表明,NSG赋予CuO-NSG大的表面积,且NSG和CuO之间存在强界面耦合。由于NSG的显著效果和NSG与CuO的协同效应,CuO-NSG显示出比CuO和CuO-还原氧化石墨烯(RGO)更高的EGO活性。基于CuO-NSG的传感器显示出优异的葡萄糖感测性能,表现出1722μA·mmol·L~(-1)·cm~(-2)的高灵敏度和0.07μmmol·L~(-1)的低检测限及在实际样品分析中的选择性、再现性、稳定性和可行性的良好检测性能。     

基于壳聚糖-纳米金粒子的生物传感器的构造与应用研究进展

对近年来基于壳聚糖-纳米金粒子的生物传感器的构造与应用研究进行了回顾与总结.在结合纳米金粒子独特的物理化学特性和壳聚糖良好的生物相容性,壳聚糖与酶及纳米金粒子等良好的结合能力特性基础上,通过不断改进电极结构,使用层-层复合技术以及添加碳纳米管或纳米金丝的方法,能构造出具有很高灵敏度和检测极限的纳米复合材料生物传感器.通过改变结合酶的品种,可以获得具有不同检测环境和检测物质适应性的生物传感器.对生物传感器的应用也进行了相应的总结.     

金属纳米颗粒在表面等离激元共振生物传感器上的应用

文章研究不同形状和长径比的金属纳米颗粒应用在表面等离激元共振（SPR）生物传感器中对传感信号的影响,自制金属纳米颗粒并进行物理表征,以金纳米颗粒与抗兔IgG进行生物偶联,利用自制角度检测型SPR生物传感器对兔IgG抗体进行检测,结果表明,金属颗粒的形状和长径比对SPR传感器的共振角都有影响,金纳米棒能够明显提高SPR生物传感器的检测灵敏度。     

基于Pt-Pb纳米花的无酶葡萄糖传感器性能研究

利用超声恒电流沉积法在金电极表面制备了Pt-Pb纳米花,并将其用于构建无酶葡萄糖传感器,采用阻抗谱、循环伏安和差分脉冲伏安法研究了其电化学性能。SEM结果表明,当沉积电流为10mA时,电极表面形成Pt-Pb纳米花结构。电化学测试结果表明,该电极对葡萄糖具有很好的电催化性能,在含有氯离子的溶液中不会失活。Pt-Pb纳米花电极构建的无酶传感器对葡萄糖的线性响应范围为0.5×10-3～22×10-3 mol/L,灵敏度为3.68mA·cm-2·(mol/L)-1,检测限为24×10-6 mol/L。此外,传感器具有良好的选择性、重复性和稳定性。     

用单壁纳米碳管制备葡萄糖生物传感器的研究

以单壁纳米碳管为代表材料,对利用纳米碳管制备葡萄糖生物传感器中纳米碳管的作用和纳米碳管修饰电极的方法、酶的固定化方法及电极种类等因素对传感器性能的影响进行了研究.研究结果表明,纳米碳管的加入能有效地改善传感器的电化学性能,利用二茂铁和单壁纳米碳管共同修饰电极所制得的传感器的性能要好于仅用单壁纳米碳管修饰电极制得的传感器.在酶的固定化方法中,戊二醛交联法要略好于明胶包埋法;而利用铂电极制备出的生物传感器对葡萄糖的响应电流要明显高于利用金电极和玻碳电极制备出的生物传感器.这些结论对于开发纳米碳管在生物传感领域及生命科学相关领域的应用有参考价值.     

导电聚合物固定酶生物传感器研究进展

导电聚合物具有良好的导电性,已成为一种酶固定的良好载体.主要综述了近年导电聚合物固定酶生物传感器,特别是导电聚合物固定酶方面所涌现出的新技术和新结构,如溶胶-凝胶技术、丝网印刷技术、纳米技术,以及多层结构、微电极、复合结构等,并指出了导电聚合物固定酶生物传感器今后的发展方向.     

基于生物素-亲和素系统的酶固定化及纳米金增效的研究

应用石英晶体微天平(QCM)研究了基于生物素一亲和素系统的葡萄糖氧化酶的固定化,探讨了纳米金修饰QCM金基片对酶固定化的一系列过程的影响。在本实验条件下,利用生物素．亲和素系统能较好地固定化葡萄糖氧化酶,经过纳米金颗粒修饰的QCM基片对酶的吸附量比未经修饰的基片可提高1倍以上。     

ZnS nanoparticles electrodeposited onto ITO electrode as a platform for fabrication of enzyme-based biosensors of glucose

The electrochemical and photoelectrochemical biosensors based on glucose oxidase (GOD) and ZnS nanoparticles modified indium tin oxide (ITO) electrode were investigated. The ZnS nanoparticles were electrodeposited directly on the surface of ITO electrode. The enzyme was immobilized on ZnS/ITO electrode surface by sol–gel method to fabricate glucose biosensor. GOD could electrocatalyze the reduction of dissolved oxygen, which resulted in a great increase of the reduction peak current. The reduction peak current decreased linearly with the addition of glucose, which could be used for glucose detection. Moreover, ZnS nanoparticles deposited on ITO electrode surface showed good photocurrent response under illumination. A photoelectrochemical biosensor for the detection of glucose was also developed by monitoring the decreases in the cathodic peak photocurrent. The results indicated that ZnS nanoparticles deposited on ITO substrate were a good candidate material for the immobilization of enzyme in glucose biosensor construction.     

Optimal environment for glucose oxidase in perfluorosulfonated ionomer membranes: improvement of first-generation biosensors

An optimal environment for glucose oxidase (GOx) in Nafion membranes is achieved using an advanced immobilization protocol based on a nonaqueous immobilization route. Exposure of glucose oxidase to water-organic mixtures with a high (85-95%) content of the organic solvent resulted in stabilization of the enzyme by a membrane-forming polyelectrolyte. Such an optimal environment leads to the highest enzyme specific activity in the resulting membrane, as desired for optimal use of the expensive oxidases. Casting solution containing glucose oxidase and Nafion is completely stable over 5 days in a refrigerator, providing almost absolute reproducibility of GOx-Nafion membranes. A glucose biosensor was prepared by casting the GOx-Nafion membranes over Prussian Blue-modified glassy carbon disk electrodes. The biosensor operated in the FIA mode allows the detection of glucose down to the 0.1 microM level, along with high sensitivity (0.05 A M(-1) cm(-2)), which is only 10 times lower than the sensitivity of the hydrogen peroxide transducer used. A comparison with the recently reported enzyme electrodes based on similar H2O2 transducers (transition metal hexacyanoferrates) shows that the proposed approach displays a dramatic (100-fold) improvement in sensitivity of the resulting biosensor. Combined with the attractive performance of a Prussian Blue-based hydrogen peroxide transducer, the proposed immobilization protocol provides a superior performance for first-generation glucose biosensors in term of sensitivity and detection limits.     

Development of bimetal-grown multi-scale carbon micro-nanofibers as an immobilizing matrix for enzymes in biosensor applications

This study describes the development of a novel bimetal (Fe and Cu)-grown hierarchical web of carbon micro-nanofiber-based electrode for biosensor applications, in particular to detect glucose in liquids. Carbon nanofibers (CNFs) are grown on activated carbon microfibers (ACFs) by chemical vapor deposition (CVD) using Cu and Fe as the metal catalysts. The transition metal-fiber composite is used as the working electrode of a biosensor applied to detect glucose in liquids. In such a bi-nanometal-grown multi-scale web of ACF/CNF, Cu nanoparticles adhere to the ACF-surface, whereas Fe nanoparticles used to catalyze the growth of nanofibers attach to the CNF tips. By ultrasonication, Fe nanoparticles are dislodged from the tips of the CNFs. Glucose oxidase (GOx) is subsequently immobilized on the tips by adsorption. The dispersion of Cu nanoparticles at the substrate surface results in increased conductivity, facilitating electron transfer from the glucose solution to the ACF surface during the enzymatic reaction with glucose. The prepared Cu-ACF/CNF/GOx electrode is characterized for various surface and physicochemical properties by different analytical techniques, including scanning electron microscopy (SEM), electron dispersive X-ray analysis (EDX), Fourier-transform infrared spectroscopy (FTIR), BET surface area analysis, and transmission electron microscopy (TEM). The electrochemical tests show that the prepared electrode has fast response current, electrochemical stability, and high electron transfer rate, corroborated by CV and calibration curves. The prepared transition metal-based carbon electrode in this study is cost-effective, simple to develop, and has a stable immobilization matrix for enzymes.     

Glucose biosensor based on carbon nanotube epoxy composites

A novel glucose biosensor based on a rigid and renewable carbon nanotube (CNT) based biocomposite is reported. The biosensor was based on the immobilization of glucose oxidase (GOx) within the CNT epoxy-composite matrix prepared by dispersion of multi-wall CNT inside the epoxy resin. The use of CNT, as the conductive part of the composite, ensures better incorporation of enzyme into the epoxy matrix and faster electron transfer rates between the enzyme and the transducer. Experimental results show that the CNT epoxy composite biosensor (GOx-CNTEC) offers an excellent sensitivity, reliable calibration profile, and stable electrochemical properties together with significantly lower detection potential (+0.55 V) than GOx-graphite epoxy composites (+0.90 V; difference deltaE = 0.35 V). The results obtained favorably compare to those of a glucose biosensor based on a graphite epoxy composite (GOx-GEC).     

Fabrication of a glucose biosensor based on citric acid assisted cobalt ferrite magnetic nanoparticles

A novel and practical glucose biosensor was fabricated with immobilization of Glucose oxidase (GOx) enzyme on the surface of citric acid (CA) assisted cobalt ferrite (CF) magnetic nanoparticles (MNPs). This innovative sensor was constructed with glassy carbon electrode which is represented as (GOx)/CA-CF/(GCE). An explicit high negative zeta potential value (-22.4 mV at pH 7.0) was observed on the surface of CA-CF MNPs. Our sensor works on the principle of detection of H2O2 which is produced by the enzymatic oxidation of glucose to gluconic acid. This sensor has tremendous potential for application in glucose biosensing due to the higher sensitivity 2.5 microA/cm2-mM and substantial increment of the anodic peak current from 0.2 microA to 10.5 microA.     

Towards nanomedicine with a supramolecular approach: a review

A review dedicated mainly to the results obtained by the authors on the use of cyclodextrin (CD) derivatives on protein (enzyme) stabilization through covalent and non-covalent interactions (host-guest supramolecular interactions) is presented here. This latter procedure served to introduce a new method for enzyme immobilization on metallic surfaces that can be used to prepare biosensors and therapeutic nanodevices. The surfaces of gold (and silver) electrodes and nanoparticles were modified with sulphur-containing cyclodextrin derivatives. The protein (enzyme) was then supramolecularly immobilized on the modified surface when one or more of its bulky hydrophobic moieties was included into the CD cavity. The protein can also be modified with a typical CD guest, such as adamantane, to achieve a more stable immobilization. Different examples are presented, such as a biosensor based on monolayers of adamantane-modified cytochrome c and a bienzymatic nanodevice comprising gold nanoparticles stabilized with CD associated to catalase and superoxide dismutase modified with complementary host-guest residues. The possibilities of this new approach for the development of biosensors and therapeutic nanodevices are analyzed.     

Titanium dioxide–cellulose hybrid nanocomposite and its glucose biosensor application

This paper investigates the fabrication of titanium dioxide (TiO₂)–cellulose hybrid nanocomposite and its possibility for a conductometric glucose biosensor. TiO₂ nanoparticles were blended with cellulose solution prepared by dissolving cotton pulp with lithium chloride/N,N-dimethylacetamide solvent to fabricate TiO₂–cellulose hybrid nanocomposite. The enzyme, glucose oxidase (GOx) was immobilized into this hybrid nanocomposite by physical adsorption method. The successful immobilization of glucose oxidase into TiO₂–cellulose hybrid nanocomposite via covalent bonding between TiO₂ and GOx was confirmed by X-ray photoelectron analysis. The linear response of the glucose biosensor is obtained in the range of 1–10 mM. This study demonstrates that TiO₂–cellulose hybrid nanocomposite can be a potential candidate for an inexpensive, flexible and disposable glucose biosensor.     

壳聚糖凝胶材料固定葡萄糖氧化酶制电极的研究

以壳聚糖为载体研究凝胶法固定葡萄糖氧化酶制电极。试验研究了载体壳聚糖的降解性；交联剂戊二醛的浓度、用量；电极的载酶量等固定化条件对所组建的传感器性能的影响。通过影响规律的分析、优化固定化条件的研究，找出了根据壳聚糖溶液粘度适当调整交联剂成二醛的用量和铂丝在酶膜母液中浸涂时间，克服壳聚糖的降解性对酶电极性能的影响，建立了制备性能相近的GOD传感器的方法。