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基于金纳米粒子/氧化铝溶胶-凝胶修饰的丝网印刷电极的安培免疫传感器,用于检测恶性疟原虫 HRP-2 抗体。

Amperometric immunosensor based on gold nanoparticles/alumina sol-gel modified screen-printed electrodes for antibodies to Plasmodium falciparum histidine rich protein-2.

机构信息

Defence Research & Development Establishment, Jhansi Road, Gwalior, 474002, India.

出版信息

Analyst. 2010 Mar;135(3):608-14. doi: 10.1039/b918880k. Epub 2010 Jan 14.

Abstract

We report herein the amperometric immunosensor for antibodies to Plasmodium falciparum histidine rich protein-2 (PfHRP-2). Screen-printed electrodes (SPEs) were modified with alumina sol-gel (Al(2)O(3) sol-gel) derived film and gold nanoparticles i.e. AuNPs/Al(2)O(3)sol-gel/SPE. A thin film was formed by dripping Al(2)O(3) sol on SPE followed by electrochemical deposition of gold nanoparticles (AuNPs). The modified SPEs were characterized by scanning electron microscopy/energy dispersive X-ray analysis (SEM-EDAX), Raman spectra and voltammetric experiments. Antibodies in rabbit serum sample were allowed to react with the PfHRP-2 protein that was immobilized on the modified SPE to form antigen-antibody immune complex (PfHRP-2/anti-PfHRP-2). The bound antibodies were quantified by alkaline phosphatase (AP) enzyme labeled secondary antibodies (anti-rabbit immunoglobulins-AP conjugate). Enzymatic substrate, 1-naphthyl phosphate was converted to 1-naphthol by AP and an electroactive product was quantified using amperometry. The performances of the developed immunosensor and Dot-ELISA were tested against different dilutions of hyper immune serum (rabbit anti-PfHRP-2). Dot ELISA and the developed immunosensor (AuNPs/Al(2)O(3)sol-gel/SPE) results for the hyper immune serum containing anti-PfHRP-2 were distinctly positive when diluted upto 8 times (1 : 12800 dilution) and 11 times (1 : 102400 dilution), respectively. The developed immunosensor was applied for antibodies to PfHRP-2 in human clinical samples.

摘要

我们在此报告了一种用于检测恶性疟原虫环子氨酸蛋白-2(PfHRP-2)抗体的电流型免疫传感器。通过氧化铝溶胶-凝胶(Al2O3溶胶-凝胶)衍生膜和金纳米粒子,即 AuNPs/Al2O3溶胶-凝胶/SPE,对丝网印刷电极(SPE)进行了修饰。通过在 SPE 上滴注 Al2O3溶胶形成薄膜,然后进行金纳米粒子的电化学沉积(AuNPs)。通过扫描电子显微镜/能量色散 X 射线分析(SEM-EDAX)、拉曼光谱和伏安实验对修饰后的 SPE 进行了表征。让兔血清样品中的抗体与固定在修饰后的 SPE 上的 PfHRP-2 蛋白发生反应,形成抗原-抗体免疫复合物(PfHRP-2/抗-PfHRP-2)。通过碱性磷酸酶(AP)酶标记的二抗(抗兔免疫球蛋白-AP 缀合物)定量结合的抗体。AP 将酶底物 1-萘基磷酸盐转化为 1-萘酚,并通过电流法对电活性产物进行定量。针对不同稀释度的高免疫血清(兔抗 PfHRP-2),对所开发的免疫传感器和 Dot-ELISA 的性能进行了测试。Dot ELISA 和开发的免疫传感器(AuNPs/Al2O3溶胶-凝胶/SPE)对含有抗 PfHRP-2 的高免疫血清的结果分别在稀释至 8 倍(1:12800 稀释)和 11 倍(1:102400 稀释)时明显呈阳性。该免疫传感器用于检测人临床样本中的 PfHRP-2 抗体。

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