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Development of a mass-producible on-chip plasmonic naeohole array biosensor

机译:发展mass-producible芯片上电浆naeohole阵列生物传感器

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We have developed a polymer film based plasmonic device whose optical properties are tuned for measuring biological samples. The device has a circular nanohole array structure fabricated with a nanoimprint technique using a UV curable polymer, and then gold thin film is deposited by electron beam deposition. Therefore, the device is mass-producible, which is also very important for bioaffinity sensors. First the gold film thickness and hole depth were optimized to obtain the maximum dip shift for the reflection spectra. The dip shift is equivalent to the sensitivity to refractive index changes at the plasmonic device surface. We also calculated the variation in reflection spectra by changing the above conditions using the finite-difference time domain method, and we obtained agreement between the theoretical and experimental curves. The nanohole periodicity was adjusted from 400 to 900 nm to make it possible to perform measurements in the visible wavelength region to measure the aqueous samples with less optical absorption. The tuned bottom filled gold nanohole array was incorporated in a microfluidic device covered with a PDMS based microchannel that was 2 mm wide and 20 μm deep. As a proof of concept, the device was used to detect TNF-α by employing a direct immunochemical reaction on the plasmonic array, and a detection limit of 21 ng mL~(- 1)was obtained by amplification with colloidal gold labeling instead of enzymatic amplification.
机译:我们已经开发出一种基于聚合物薄膜的电浆设备的光学性能调优测量生物样本。圆形nanohole数组结构制造使用紫外线固化nanoimprint技术聚合物,然后金薄膜沉积电子束沉积。mass-producible,这也很重要呢bioaffinity传感器。厚度和孔深度进行优化来获得反射光谱的最大倾斜转变。下降的转变相当于敏感性折射率变化的电浆设备表面。通过改变上述反射光谱使用有限差分时间条件域方法,和我们之间的协议理论和实验曲线。从400年到900年nanohole周期性调整纳米可以执行测量可见波长测量区域用更少的光学吸收水样本。调底了黄金nanohole数组合并在一个微流控设备覆盖与基于PDMS微通道2毫米宽和20μm深。被用来检测肿瘤坏死因子-α采用直接吗免疫化学反应的电浆数组,的检出限21 ng毫升~ (- 1)通过放大与胶体金标签代替酶放大。

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