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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Divalent ion-induced aggregation of gold nanoparticles for voltammetry Immunosensing: comparison of transducer signals in an assay for the squamous cell carcinoma antigen
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Divalent ion-induced aggregation of gold nanoparticles for voltammetry Immunosensing: comparison of transducer signals in an assay for the squamous cell carcinoma antigen

机译:二价离子诱导的金纳米颗粒用于伏安法免疫溶解的聚集:换能器信号在鳞状细胞癌抗原的测定中的比较

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A method is described for the electrochemical determination of squamous cell carcinoma (SCC) antigen, and by testing the effect of 30 nm gold nanoparticles (GNPs). Three comparative studies were performed in the presence and absence of GNPs, and with agglomerated GNPs. The divalent ion Ca(II) was used to induce a strong agglomeration of GNPs, as confirmed by colorimetry and voltammetry. Herein, colorimetry was used to test the best amount of salt needed to aggregate the GNPs. Despite, voltammetry was used to determine the status of biomolecules on the sensor. The topography of the surface of ZnO-coated interdigitated electrodes was analyzed by using 3D-nano profilometry, scanning electron microscopy, atomic force microscopy and high-power microscopy. The interaction between SCC antigen and antibody trigger vibrations on the sensor and cause dipole moment, which was measured using a picoammeter with a linear sweep from 0 to 2 V at 0.01 V step voltage. The sensitivity level was 10 fM by 3 sigma calculation for the dispersed GNP-conjugated antigen. This indicates a 100-fold enhancement compared to the condition without GNP conjugation. However, the sensitivity level for agglomerated GNPs conjugated antibody was not significant with 100 fM sensitivity. Specificity was tested for other proteins in serum, namely blood clotting factor IX, C-reactive protein, and serum albumin. The SCC antigen was quantified in spiked serum and gave recoveries that ranged between 80 and 90%.
机译:描述了用于鳞状细胞癌(SCC)抗原的电化学测定的方法,并通过测试30nM金纳米颗粒(GNP)的效果。在存在和不存在GNPS中进行三项比较研究,并用附聚的GNPS进行。二价离子Ca(II)用于诱导GNP的强凝聚,如色比例和伏安法证实。在此,使用比色法测试聚集GNP所需的最佳盐。尽管如此,伏安法用于确定传感器上的生物分子的状态。通过使用3D纳米轮廓测定法,扫描电子显微镜,原子力显微镜和高功率显微镜分析ZnO涂覆的齐键电极表面的地形。 SCC抗原和抗体之间的相互作用在传感器上触发振动并引起偶极矩,用线性扫描从0至2V的微扫描器以0.01V步进测量。敏感性水平为分散的GNP缀合抗原的3秒形计算为10 fm。与没有GNP缀合的条件相比,这表明100倍的增强。然而,凝聚的GNPS共轭抗体的敏感性水平与100cm敏感性不显着。对血清中的其他蛋白质进行测试,即血液凝固因子IX,C反应蛋白和血清白蛋白的特异性。 SCC抗原在尖刺的血清中量化,并在80%和90%之间进行了回收率。

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