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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >A highly sensitive prostate-specific antigen immunosensor based on gold nanoparticles/PAMAM dendrimer loaded on MWCNTS/chitosan/ ionic liquid nanocomposite
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A highly sensitive prostate-specific antigen immunosensor based on gold nanoparticles/PAMAM dendrimer loaded on MWCNTS/chitosan/ ionic liquid nanocomposite

机译:基于负载在MWCNTS /壳聚糖/离子液体纳米复合材料上的金纳米颗粒/ PAMAM树状大分子的高敏感性前列腺特异性抗原免疫传感器

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摘要

We have developed a sensitive electrochemical immunosensor for the detection of prostate-specific antigen (PSA), based on covalently immobilizing of anti-PSA and redox mediator (thionine) onto gold nanoparticles-incorporated polyamidoamine dendrimer (AuNPs-PAMAM) and multiwalled carbon nano-tubes/ionic liquid/chitosan nanocomposite (MWCNTs/IL/Chit) as the support platform. The MWCNTs/IL/ Chit nanocomposite and synthesized AuNPs were characterized using SEM and TEM microscopy techniques. Greatly amplified immunoassay was established by sandwiching the antigen between anti-PSA immobilized on the MWCNTs/IL/Chit/AuNPs-PAMAM interface and anti-PSA labeled with horseradish peroxidase (HRP-labeled anti-PSA) as secondary antibody. Phtaloyl chloride (Ph) was used as linking agent for the subsequent immobilization of AuNPs-PAMAM onto platform and anti-PSA antibody and thionine onto AuNPs-PAMAM dendrimer. The increased electrocatalytic reduction of H_20_2 by HRP was monitored by differential pulse voltammetry technique. Under optimized condition the calibration curve for PSA concentration was linear up to 80 ng ml~(-1) with detection limit (signal-to-noise ratio of 3) of 1 pg ml(-1). AuNPs-PAMAM dendrimer as platform not only increased the amount of thionine and PSA antibody but also the electron transfer process accelerated by encapsulated AuNPs. Moreover, the proposed PSA immunosensor exhibited excellent stability and reproducibility. Accurate detection of PSA in human serum samples was demonstrated by comparison to standard ELISA assays. In addition, impedance technique was used as simple, rapid, low cost label free analytical method for PSA measurement with detection limit of 0.5ngml~(-1) at concentration range up to 25ng ml~(-1). The results indicate that the present protocol is quite promising in developing other electrochemical immunosensors.
机译:我们已将抗PSA和氧化还原介体(硫氨酸)共价固定在掺有金纳米颗粒的聚酰胺酸胺树枝状大分子(AuNPs-PAMAM)和多壁碳纳米管上,开发了一种用于检测前列腺特异性抗原(PSA)的灵敏电化学免疫传感器。管/离子液体/壳聚糖纳米复合材料(MWCNTs / IL / Chit)作为支撑平台。使用SEM和TEM显微镜技术对MWCNTs / IL / Chit纳米复合材料和合成的AuNPs进行了表征。通过将抗原夹在固定在MWCNTs / IL / Chit / AuNPs-PAMAM接口上的抗PSA和以辣根过氧化物酶标记的抗PSA(HRP标记的抗PSA)之间进行夹心,从而建立了高度扩增的免疫测定法。邻苯二甲酰氯(Ph)被用作连接剂,随后将AuNPs-PAMAM固定在平台和抗PSA抗体上,将硫氨酸固定到AuNPs-PAMAM树枝状大分子上。用差示脉冲伏安法监测了HRP对H_20_2的电催化还原反应。在最佳条件下,PSA浓度的校准曲线在不超过80 ng ml〜(-1)的条件下呈线性,检测极限(信噪比为3)为1 pg ml(-1)。 AuNPs-PAMAM树枝状大分子作为平台,不仅增加了蛋氨酸和PSA抗体的量,而且通过包封的AuNPs加速了电子转移过程。而且,提出的PSA免疫传感器表现出优异的稳定性和可再现性。通过与标准ELISA分析相比较,证明了在人血清样品中PSA的准确检测。此外,阻抗技术被用作简单,快速,低成本的无标签分析方法,用于PSA测量,在浓度范围高达25ng ml〜(-1)时检测限为0.5ngml〜(-1)。结果表明,本协议在开发其他电化学免疫传感器方面非常有前途。

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