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基于蛋白质功能化自组装单层的用于结肠癌检测的生物传感器。

Protein functionalised self assembled monolayer based biosensor for colon cancer detection.

机构信息

Nanobioelectronics Laboratory, Department of Biotechnology, Delhi Technological University, Delhi, 110042, India.

Nanobioelectronics Laboratory, Department of Biotechnology, Delhi Technological University, Delhi, 110042, India; Centre for Nano Science and Engineering (CeNSE), Indian Institute of Science, Bengaluru, 560012, India.

出版信息

Talanta. 2019 Aug 15;201:465-473. doi: 10.1016/j.talanta.2019.04.039. Epub 2019 Apr 18.

Abstract

We report results of the studies relating to the fabrication of a surface plasmon resonance (SPR) based label-free immunosensor for real-time monitoring of endothelin-1 (ET-1), a colon cancer biomarker. A gold disk modified with a self-assembled monolayer (SAM) of 11-mercaptoundecanoic acid (11-MUA) was functionalised via covalent immobilization of monoclonal anti-ET-1 antibodies using EDC-NHS (1-(3-(dimethylamine)-propyl)-3-ethylcarbodiimide hydrochloride, N-hydroxy succinimide) chemistry. This immunosensing platform (ethanolamine/anti-ET-1/11-MUA/Au) was characterized via atomic force microscopy (AFM), contact angle (CA) and Fourier transform infrared (FT-IR) spectroscopic techniques. The fabricated SPR electrode was further used to detect ET-1 in the broad concentration range 2-100 pg mL, with a detection limit of 0.30 pg mL and remarkable sensitivity of 2.18 m pgmL. The adsorption mechanism was studied using monophasic model and the values of association (k) and dissociation (k) constants for anti-ET-1 and ET-1 binding were calculated to be 4.4 ± 0.4 × 10 M s and 2.04 ± 0.0003 × 10 s, respectively. The results obtained via analysis of serum samples of colorectal cancer patients were found to be in good agreement with those obtained from enzyme-linked immunosorbent assay (ELISA) technique. Further, electrochemical studies were performed to prove the efficacy of the fabricated platform as a point of care device for the detection of ET-1.

摘要

我们报告了与基于表面等离子体共振(SPR)的无标记免疫传感器的制造相关的研究结果,该传感器用于实时监测结肠癌生物标志物内皮素-1(ET-1)。通过使用 EDC-NHS(1-(3-(二甲氨基)丙基)-3-乙基碳二亚胺盐酸盐,N-羟基琥珀酰亚胺)化学将金盘与 11-巯基十一酸(11-MUA)的自组装单层(SAM)功能化。通过原子力显微镜(AFM)、接触角(CA)和傅里叶变换红外(FT-IR)光谱技术对该免疫传感平台(乙醇胺/抗 ET-1/11-MUA/Au)进行了表征。进一步将制造的 SPR 电极用于在 2-100 pg mL 的宽浓度范围内检测 ET-1,检测限为 0.30 pg mL,灵敏度高达 2.18 m pg mL。使用单相模型研究了吸附机制,并计算了抗 ET-1 和 ET-1 结合的结合(k)和解离(k)常数的值,分别为 4.4±0.4×10 M s和 2.04±0.0003×10 s。通过分析结直肠癌患者的血清样本得到的结果与酶联免疫吸附测定(ELISA)技术得到的结果非常吻合。此外,还进行了电化学研究,以证明所制造平台作为用于检测 ET-1 的即时护理设备的功效。

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