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一种基于分子印迹纳米粒子作为识别元件的新型电容传感器。

A novel capacitive sensor based on molecularly imprinted nanoparticles as recognition elements.

机构信息

MIP Diagnostics Ltd., Fielding Johnson Building, University of Leicester, LE1 7RH, United Kingdom.

MIP Diagnostics Ltd., Fielding Johnson Building, University of Leicester, LE1 7RH, United Kingdom.

出版信息

Biosens Bioelectron. 2018 Nov 30;120:108-114. doi: 10.1016/j.bios.2018.07.070. Epub 2018 Aug 7.

Abstract

Molecularly Imprinted Polymers (MIPs) are synthetic receptors capable of selective binding to their target (template) molecules and, hence, are used as recognition elements in assays and sensors as a replacement for relatively unstable enzymes and antibodies. Herein, we describe a manufacturing-friendly protocol for integration of MIP nanoparticles (nanoMIPs) with a (label-free) capacitive sensor. The nanoMIPs were produced by solid-phase synthesis for two templates with different sizes and properties, including a small molecule tetrahydrocannabinol (THC) and a protein (trypsin). NanoMIPs were deposited on the surface of the sensor and the change in capacitance (ΔC) upon binding of the target was measured. The significant improvement in the selectivity and limit of detection (one order of magnitude compared to previously used MIP microparticles) can be attributed to their increased surface-to-volume ratio and higher specificity of the nanoMIPs produced by the solid-phase method. The methodology described is also compatible with common sensor fabrication approaches, as opposed to methods involving in situ MIP polymerisation. The proposed sensor shows high selectivity, fast sensor response (45 min including injection, regeneration and re-equilibration with running buffer), and straightforward data analysis, which makes it viable for label-free monitoring in real-time. The set of targets assessed in this manuscript shows the general applicability of the biosensor platform.

摘要

分子印迹聚合物(MIPs)是一种能够选择性结合其目标(模板)分子的合成受体,因此可用作分析和传感器中的识别元件,以替代相对不稳定的酶和抗体。在此,我们描述了一种制造友好型方案,将 MIP 纳米颗粒(nanoMIPs)与(无标记)电容传感器集成。通过固相合成法制备了两种具有不同尺寸和特性的模板的 nanoMIPs,包括小分子四氢大麻酚(THC)和蛋白质(胰蛋白酶)。将 nanoMIPs 沉积在传感器表面上,并测量结合目标时电容的变化(ΔC)。与之前使用的 MIP 微颗粒相比,选择性和检测限(提高了一个数量级)的显著改善归因于它们增加的表面积与体积比,以及固相法制备的 nanoMIPs 的更高特异性。所描述的方法也与常见的传感器制造方法兼容,而不是涉及原位 MIP 聚合的方法。与实时无标记监测相比,该传感器具有高选择性、快速传感器响应(包括注射、再生和用运行缓冲液重新平衡在内的 45 分钟)和简单的数据分析,使其具有可行性。在本文评估的目标组中显示了生物传感器平台的通用性。

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