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采用纳米压印光刻技术实现的等离子体金纳米盘阵列的高灵敏度生物传感。

Highly sensitive biosensing using arrays of plasmonic Au nanodisks realized by nanoimprint lithography.

机构信息

Korea Research Institute of Bioscience and Biotechnology, 111 Gwahangno, Yuseong-gu, Daejeon 305-806, South Korea.

出版信息

ACS Nano. 2011 Feb 22;5(2):897-904. doi: 10.1021/nn102041m. Epub 2011 Jan 11.

DOI:10.1021/nn102041m
PMID:21222487
Abstract

We describe the fabrication of elliptical Au nanodisk arrays as a localized surface plasmon resonance (LSPR) sensing substrate for clinical immunoassay via thermal nanoimprint lithography (NIL) and enhancement in the sensitivity of the detection of the prostate-specific antigen (PSA) using the precipitation of 5-bromo-4-chloro-3-indolyl phosphate p-toluidine/nitro blue tetrazolium (BCIP/NBT), catalyzed by alkaline phosphatase. Au nanodisks were fabricated on glass through an unconventional tilted evaporation, which could preserve the thickness of imprinted resists and create an undercut beneficial to the subsequent lift-off process without any damage to pattern dimension and the glass while removing the residual polymers. To investigate the optically anisotropic property of the LSPR sensors, a probe light with linear polarization parallel to and perpendicular to the long axis of the elliptical nanodisk array was utilized, and their sensitivity to the bulk refractive index (RI) was measured as 327 and 167 nm/RIU, respectively. To our knowledge, this is the first application of enzyme-substrate reaction to sandwich immunoassay-based LSPR biosensors that previously suffered from a low sensitivity due to the short penetration depth of the plasmon field, especially when large-sized antibodies were used as bioreceptors. As a result, a large change in local refractive index because of the precipitation on the Au nanodisks amplified the wavelength shift of the LSPR peak in the vis-NIR spectrum, resulting in femtomolar detection limits, which was ∼10(5)-fold lower than the label-free detection without the enzyme precipitation. This method can be extended easily to the other clinical diagnostics with a high sensitivity.

摘要

我们通过热纳米压印光刻(NIL)制造了椭圆金纳米盘阵列作为局部表面等离子体共振(LSPR)传感基底,并通过碱性磷酸酶催化的 5-溴-4-氯-3-吲哚磷酸对甲苯胺/硝基蓝四唑(BCIP/NBT)沉淀,提高了前列腺特异性抗原(PSA)检测的灵敏度。通过非传统的倾斜蒸发在玻璃上制造了 Au 纳米盘,这可以保留压印抗蚀剂的厚度,并创建一个有利于后续脱模过程的底切,而不会对图案尺寸和玻璃造成任何损坏,同时去除残留聚合物。为了研究 LSPR 传感器的各向异性光学性质,我们使用了与椭圆纳米盘阵列的长轴平行和垂直的线偏振探针光,并测量了它们对体折射率(RI)的灵敏度,分别为 327 和 167nm/RIU。据我们所知,这是酶底物反应首次应用于基于夹心免疫测定的 LSPR 生物传感器,由于等离子体场的短穿透深度,之前这种生物传感器的灵敏度较低,尤其是当使用大尺寸抗体作为生物受体时。结果,由于 Au 纳米盘上的沉淀,局部折射率的大幅变化放大了可见近红外光谱中 LSPR 峰的波长位移,从而实现了飞摩尔检测限,比没有酶沉淀的无标记检测低约 10^5 倍。这种方法可以很容易地扩展到其他具有高灵敏度的临床诊断。

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