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1.
A sensitive enzymatic biosensor has been developed for the detection of hydrogen peroxide (H2O2), nitrite ( ) and trichloroacetic acid (TCA) by using hemoglobin (Hb) immobilized on activated screen printed carbon electrode (ASPCE) and zinc oxide (ZnO) composite. A pair of well defined redox peaks is observed with a heterogeneous electron transfer rate constant (Ks) of 5.27 s?1 for Hb at ASPCE/ZnO. The biosensor exhibits the detection of H2O2, TCA and in the concentration range of 0.5–129.5 µmol L?1, 2.5–72.5 mmol L?1 and 0.2–674 µmol L?1 with the detection limit of 0.083 µmol L?1, 0.12 mmol L?1 and 0.069 µmol L?1, respectively.  相似文献   

2.
The nickel tetrasulfonated phthalocyanine (NiTsPc) functionalized multiwalled carbon nanotube (MWCNT) nanocomposite was prepared by a simple sonochemical method. Here, NiTsPc served as a dispersing agent for MWCNT via π? π interaction between MWCNT and NiTsPc. The activated glassy carbon electrode (AGCE) modified with MWCNT‐NiTsPc composite exhibited a good electrocatalytic ability toward dopamine and displayed a good linear dependence in the concentration range of 20 nM–1.384 mM with a sensitivity of 0.17 µA µM?1 cm?2. The detection limit is 1 nM based on the signal‐to‐noise ratio of 3.  相似文献   

3.
《Electroanalysis》2005,17(9):744-748
Magnetic nanoparticles of Fe3O4 approximately 5nm in size were synthesized and characterized by XRD and TEM. A novel gold electrode modified with Fe3O4 nanoparticles was then constructed and was characterized by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The modified electrode exhibited strong promoting effect and high stability toward the electrochemical oxidation of dopamine (DA), which gave reversible redox peaks with a formal potential of 0.192 V (vs. Ag/AgCl) electrode in pH 7.0 phosphate buffer solution (PB). The anodic peak currents (measured by constant potential amperometry) increased linearly with the concentration of dopamine in the range of 1.5×10?7 to 4.0×10?4 M. The detection limit (S/N=3) obtained was 3.0×10?8 M. The relative standard deviation (RSD) of 8 successive scans was 3.41% for 1.5×10?6 M DA. The interference of ascorbic acid (AA) could be eliminated efficiently. The proposed method showed excellent sensitivity and recovery.  相似文献   

4.
建立了多壁碳纳米管及氧化锌纳米复合物修饰的丝印电极(MWNTs-ZnO SPE)测定去甲肾上腺素(NE)的方法。利用丝网印刷技术制备即抛型MWNTs-ZnO丝印电极,去甲肾上腺素在此电极上0.28 V处可产生灵敏的响应电流。应用方波伏安法测定NE的线性范围为0.75~50μmol/L,r2=0.999 3,检出限(S/N=3)为0.3μmol/L。该法简单、快速、灵敏,且电极成本低、可批量制作,适用于大批量样品中NE的测定。  相似文献   

5.
制备了对氨基苯硼酸修饰的磁性纳米粒子,其与血液中的糖化血红蛋白(Hb A1c)结合,通过网状玻璃态碳(RVC)电极的磁性区域后,可实现与未糖基化的血红蛋白分离。通过壳聚糖(CS)、正硅酸乙酯(TEOS)和碳纳米管构成的溶胶-凝胶膜修饰丝网印刷电极对血红蛋白进行电化学检测,从而建立了一种用于检测糖化血红蛋白的新方法。在0.10 V电位下,丝网印刷电极的电量与Hb A1c和Hb的浓度有较好的线性关系,检出限分别为6 mg/m L和0.05 mg/m L。该方法电极制作简单,有较好的重现性和稳定性,且能有效排除抗坏血酸(AA)、尿酸(UA)等的干扰,已成功应用于实际样品中Hb A1c的检测。  相似文献   

6.
We report here a simple and easy electrochemical approach for sensitive detection of non‐electroactive melamine using a disposable screen printed carbon electrode (SPCE) with uric acid as the recognition element. It is based on the competitive adsorptive behavior of melamine at the preanodized SPCE causing suppression in the oxidation current of uric acid. A linear range up to 126 ppb with a detection limit of 1.6 ppb (S/N=3) is achieved at the preanodized SPCE by differential pulse voltammetry. The electrochemical method is successfully applied to detect the melamine content in tainted milk powder and dog food.  相似文献   

7.
纳米银粒子修饰电极法测定血红蛋白   总被引:19,自引:0,他引:19  
报道了一种利用纳米材料修饰电极检测血红蛋白的新方法。制作了以纳米银粒子修饰的银电极,并研究了血红蛋白在该修饰电极上的直接电化学行为。实验结果表明,血红蛋白在该修饰电极上具有良好的电流响应。在2.0×10-7~1.0×10-5mol/L浓度范围内,血红蛋白的氧化峰电流与其浓度呈良好线性关系;检出限为7.4×10-8mol/L。研究了该修饰电极对血红蛋白的催化机理,利用该电极所建立的方法实现了对血红蛋白的分析测定。  相似文献   

8.
研究使用电化学沉积法在丝网印刷碳电极表面制备了还原氧化石墨烯和金纳米颗粒,构建了一种用于新冠病毒检测的石墨烯电化学传感器。通过扫描电子显微镜(SEM)和相应的电化学方法对纳米复合材料在电极表面的成功修饰进行了表征分析。并采用差分脉冲伏安法对传感器的性能进行检测,实验构建的电化学传感器具有良好的灵敏度,该传感器检线性范围为10-10-10-6mol/L,具有良好的重复性和特异性。  相似文献   

9.
A total PSA (tPSA) assay using magnetic beads (1 µm) and a re‐usable 8‐channel screen printed electrochemical array is here reported. The reaction scheme is based on a one step sandwich assay. The linear range obtained is comprised between 5 and 100 ng/mL of tPSA and have a limit of detection of 1.86 ng/mL. This methodology was validated, performing determination of tPSA in serum and the results were compared with a commercial ELISA kit.  相似文献   

10.
在银纳米粒子存在下, 多巴胺可还原硝酸银生成银, 导致银纳米粒子粒径增大, 从而使溶液颜色发生改变. 基于此, 提出了一种用于检测多巴胺的纳米银比色法. 随着多巴胺浓度的增大, 溶液的颜色由浅黄色逐渐变为深黄色, 银纳米粒子溶液的吸收峰发生红移且吸光度增大. 在最优实验条件下, 该方法检测多巴胺的线性范围为0.05~16 μmol/L, 检出限为0.04 μmol/L. 该方法操作简单、 灵敏且选择性良好, 可用于人血清中多巴胺的检测.  相似文献   

11.
利用电聚合法和脉冲沉积技术制备了纳米银/聚多巴胺修饰的玻碳电极. 通过循环伏安法和示差脉冲伏安法研究了该修饰电极上对硝基苯酚的电化学行为; 讨论了扫描速度和支持电解质等条件对对硝基苯酚在修饰电极上催化还原的影响. 结果表明, 对硝基苯酚的示差脉冲峰电流在4×10-5~3×10-4 mol/L范围内呈良好的线性关系.  相似文献   

12.
A convenient, low cost, and sensitive electrochemical method, based on a disposable graphene nanosheets (GR) and NiO nanoparticles modified carbon screen printed electrode (NiO/GR/SPE), is described for the simultaneous determination of dopamine (DA) and uric acid (UA). The modified electrode exhibited good electrocatalytic properties toward the oxidation of DA and UA. A peak potential difference of 150 mV between DA and UA was large enough to determine DA and UA individually and simultaneously. The anodic peak currents of DA were found to be linear in the concentration range of 1.0–500.0 μM with the detection limit of 3.14×10?7 M.  相似文献   

13.
This paper presents a new approach to detect dopamine in nanomolar range using an electrochemical sensor utilizing a composite made of chitosan‐stabilized silver nanoparticles and p‐toluene sulfonic acid‐doped ultrathin polypyrrole film. Studies included cyclic voltammogram, amperometry, differential pulse voltammetry and also investigation by electrochemical impedance spectroscopy. A detection limit of 0.58 nM was achieved in the linear range 1×10?9 M to 1.2×10?7 M. High sensitivity towards DA, good reproducibility and long‐term stability have been demonstrated without interference from ascorbic acid, uric acid, epinephrine, L ‐dopa, glucose. The sensing system was successfully applied for quantitative determination of dopamine in commercially available human blood serum.  相似文献   

14.
We report the electrochemical detection of captopril on commercially available screen printed electrodes (GSPE); it exploits the silver residue left behind on a GSPE during its manufacturing process and involves the catalytic formation of the silver thiol complex (Ag++RSH→AgSR+H+) at potentials corresponding to the oxidation of silver. The oxidation of the silver thiol complex was found to vary linearly with the captopril concentration up to 0.8 mM. A sensitivity of 13.34±0.58 μA mM?1 is reported with a limit of detection of 4.27±0.18 μM.  相似文献   

15.
采用循环伏安法在丝网印刷碳电极表面电聚合聚苯胺/壳聚糖复合膜,利用静电吸附作用固定烯效唑抗体,制备了检测烯效唑的阻抗型免疫传感器.采用循环伏安法和电化学阻抗谱对电极修饰过程进行了表征,并考察了缓冲溶液pH值、温育温度及时间对免疫反应的影响.在优化的条件下研究了免疫传感器的性能.此免疫传感器具有灵敏度高、特异性强、重现性和稳定性好的特点,对烯效唑的线性检测范围为0.01 ~100 mg/L,相关系数为0.999,检出限为8μg/L(3σ).白菜样品中添加0.05,0.10和1.0 mg/kg烯效唑,平均回收率为98.5% ~ 104.6%,相对标准偏差为3.3% ~4.3%,检测结果与气相色谱法的检测结果相符.  相似文献   

16.
刘莉  刘美芳  刘涛  李丽敏 《化学通报》2015,78(10):907-911
通过NaBH4还原AgNO3得到胶体银纳米粒子,制作了以该纳米粒子修饰的银电极。研究了银纳米粒子修饰银电极在电催化中的应用,并对相关机理进行了探讨。该修饰电极对醋酸具有电催化活性,但酪氨酸却对该催化信号有明显的抑制作用,因此建立了用胶体银纳米粒子修饰银电极在NaAc-HAc缓冲溶液中检测酪氨酸的方法,并讨论了最佳工作条件。结果表明:在pH = 5.5时,峰电流与酪氨酸的浓度在1.0×10-8~1.0×10-3mol L-1 范围内呈良好的线性关系,检出限为4.2×10-9 mol L-1,线性回归方程为Ip (μA) = 7.64 pC – 15.69 ( R = 99.73% )。用该方法检测氨基酸注射液中酪氨酸的含量,加标回收率在95.2%~107.8%之间。  相似文献   

17.
制备了介孔炭/纳米金修饰玻碳电极,并对对苯二酚(HQ)在该修饰电极上的电化学行为进行了研究。与HQ在纯介孔炭材料修饰玻碳电极上的电化学响应相比,HQ在该修饰电极上的氧化峰和还原峰电流均大大增加,表明纳米金与介孔炭复合后对HQ具有良好的催化作用。HQ在该修饰电极上经过富集后,峰电流明显增大。采用循环伏安法对HQ电化学行为进行研究,结果表明,HQ在3.0×10-8~1.0×10-6mol/L和1.0×10-6~1.0×10-4mol/L浓度范围内与峰电流呈良好的线性关系,据此建立了检测HQ的电化学分析方法。该方法的相对标准偏差为0.69%,检出限(S/N=3)为1.0×10-8mol/L,具有较高的稳定性和灵敏度。  相似文献   

18.
A novel synthesized tetraamino cobalt(II) phthalocyanine monomer was used for the fabrication of a sensor by electrochemical polymerization. A disposable electrochemical sensor based on the use of a screen printed carbon electrode covered with an electropolymerized film of tetraamino cobalt(II) phthalocyanine for the determination of L-dopa in pharmaceutical tablets and biological samples was described. Cyclic voltammetry and electrochemical impedance spectroscopy were performed for the characterization of the bare and modified electrode. For the electrochemical detection of L-dopa differential pulse voltammetry was used. The proposed method exhibits a good response towards electrooxidation of L-dopa in the linear concentration range: from 0.1 to 1000.0 μmol L−1 in BRB pH=2.0, with a detection limit of 0.03 μmol L−1 and from 1 to 1000 μmol L−1 in PBS pH=7.4, with a detection limit of 0.33 μmol L−1. Due to the fact that the developed sensor was applied in two different types of real samples, two buffer media were used, BRB pH=2.0 for pharmaceutical and urine samples and PBS pH=7.4 for whole blood samples. The proposed pCoTAPc/SPCE was successfully applied for the determination of L-dopa in pharmaceutical tablets, urine and in whole blood samples with satisfactory results.  相似文献   

19.
Screen printed carbon electrodes (SPCEs) modified by a combination of chitosan, multi walled carbon nanotubes (MWCNTs) and zinc nanoparticles (ZnNPs) were studied for the first time as a suitable candidate for non-enzymatic insulin determination. In an effort to find the most suitable modification for electrochemical insulin determination, the stability, analytical characteristics, and selectivity were determined. The results confirmed that the ZnNPs/chitosan-MWCNTs prepared with the Zn deposition time of 45 s displayed the best electrocatalytic activity towards insulin oxidation in a wide linear concentration range (0.5 μM to 5 μM), with low limit of detection and high sensitivity.  相似文献   

20.
印刷三电极系统的制备及分析应用   总被引:4,自引:2,他引:4  
汪立忠  张玉涛 《分析化学》1994,22(11):1185-1188
用丝网印刷技术制备了条形三电极系统,在盐酸、柠檬酸和抗坏血酸支持电解质中二次微分阳极溶出伏安法测定痕量铜。对其电化学行为和响应与电极参数之间的关系作了较为详细的讨论。富集3min,线性范围1.1 ̄50μg/L;检测下限1.1μg/L;10次重复测定值相对标准偏差为2.6%。简便易制、价廉、集约化等特点使印刷电极可能在化学修饰电极、生物传感器方面得到实际的应用。  相似文献   

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