使用磁性磺化还原氧化石墨烯/金纳米粒子适体传感器检测前列腺特异性抗原

Iman Ahmadi , Mehrab Pourmadadi , Fatemeh Yazdian , Hamid Rashedi , Abbas Rahdar , Sadanand Pandey
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引用次数: 0

摘要

前列腺特异性抗原(PSA)是一种由前列腺癌细胞产生的蛋白质,它的存在可能预示着前列腺癌的可能性。为了检测PSA,开发了一种利用磁性磺化还原氧化石墨烯/金纳米颗粒的新型感应传感器。这种独特的纳米复合材料首次用于前列腺癌的生物传感,显著提高了生物传感器的性能。与以前的工作不同,我们的生物传感器包含两种检测模式:亚铁氰化物溶液中的无标记检测模式和使用亚甲基蓝的标记模式。利用红外光谱(FTIR)、x射线衍射(XRD)和透射电镜(TEM)等测试手段对纳米颗粒的性质进行了识别,并确定了颗粒之间的联系。为了检测不同阶段的适体传感器,采用了一系列电分析技术,如循环伏安法(CV)、方波伏安法(SWV)和电化学阻抗谱法(EIS)。该配体传感器对PSA具有显著的选择性,能够将PSA与葡萄糖、癌胚抗原(CEA)等其他成分区分开来。最终在亚铁氰化物环境中检出限(LOD)为1.371 ng/mL, R2为0.9777。磷酸缓冲液中标记电极的检出限为1.566 pg/mL, R2值为0.9676,线性范围为2.5 ~ 12.5 pg/mL,具有较高的灵敏度和准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of prostate specific antigen using a magnetic sulfonated reduced graphene oxide/gold nanoparticle aptasensor

Prostate-specific antigen (PSA), is a protein produced by cancerous cells in the prostate gland, and its presence may indicate the likelihood of prostate cancer. For the purpose of detecting PSA, an innovative aptasensor utilizing magnetic sulfonated reduced graphene oxide/gold nanoparticles was developed. This unique nanocomposite has been used for the first time for biosensing of prostate cancer which resulted in significant enhancement of the biosensor’s performance. Unlike previous works, our biosensor incorporates two detection modes: a label-free detection mode in ferrocyanide solution and a labeled mode using methylene blue. Different tests such as FTIR, XRD and TEM were applied to recognize the characterization of the nanoparticles and to make sure of the linkage of particles. To examine the aptasensor at various stages, a range of electroanalytical techniques, such as cyclic voltammetry (CV), square-wave voltammetry (SWV), and electrochemical impedance spectroscopy (EIS), were employed. The aptasensor exhibited significant selectivity for PSA, as demonstrated by its ability to distinguish PSA from other components like glucose, carcinoembryonic antigen (CEA), etc. Ultimately, the detection limit (LOD) reached 1.371 ng/mL in the ferrocyanide environment with an R2 value of 0.9777. Furthermore, the labeled electrode in phosphate buffer achieved the remarkable detection limit of 1.566 pg/mL with an R2 value of 0.9676 and linear range of 2.5–12.5 pg/mL, demonstrating the impressive sensitivity and accuracy of the method.

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