Department of Physics, Tsinghua University, Beijing 100084, China; Shenzhen Key Laboratory for Minimal Invasive Medical Technologies, Institute of Optical imaging and Sensing, Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055, China.
Department of Physics, Tsinghua University, Beijing 100084, China; Shenzhen Key Laboratory for Minimal Invasive Medical Technologies, Institute of Optical imaging and Sensing, Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055, China.
Biosens Bioelectron. 2017 Aug 15;94:328-334. doi: 10.1016/j.bios.2017.03.021. Epub 2017 Mar 10.
A new type of sensing protocol, based on a high precision metrology of quantum weak measurement, was first proposed for molecularly imprinted polymers (MIP) sensor. The feasibility, sensitivity and selectivity of weak measurement based MIP (WMMIP) sensor were experimentally demonstrated with bovine serum albumin (BSA). Weak measurement system exhibits high sensitivity to the optical phase shift corresponding to the refractive index change, which is induced by the specific capture of target protein molecules with its recognition sites. The recognition process can be finally characterized by the central wavelength shift of output spectra through weak value amplification. In our experiment, we prepared BSA@MIP with modified reversed-phase microemulsion method, and coated it on the internal surface of measuring channels assembled into the Mach-Zehnder (MZ) interferometer based optical weak measurement system. The design of this home-built optical system makes it possible to detect analyte in real time. The dynamic process of the specific adsorption and concentration response to BSA from 5×10 to 5×10μg/L was achieved with a limit of detection (LOD) of 8.01×10g/L. This WMMIP shows superiority in accuracy, fast response and low cost. Furthermore, real-time monitoring system can creatively promote the performance of MIP in molecular analysis.
一种基于高精度量子弱测量计量的新型传感协议,首次被应用于分子印迹聚合物(MIP)传感器。实验证明,基于弱测量的分子印迹聚合物(WMMIP)传感器具有可行性、灵敏度和选择性,其研究对象为牛血清白蛋白(BSA)。弱测量系统对光学相移具有很高的灵敏度,该光学相移对应于折射率变化,而折射率变化是由目标蛋白分子与识别位点的特异性结合引起的。通过弱值放大,可以最终通过输出光谱的中心波长移动来表征识别过程。在我们的实验中,我们使用改进的反相微乳液法制备了 BSA@MIP,并将其涂覆在组装成基于 Mach-Zehnder(MZ)干涉仪的光学弱测量系统的测量通道的内表面上。该自制光学系统的设计使得实时检测分析物成为可能。从 5×10 到 5×10μg/L,实现了对 BSA 的特异性吸附和浓度响应的动态过程,检测限(LOD)为 8.01×10g/L。这种 WMMIP 在准确性、快速响应和低成本方面具有优势。此外,实时监测系统可以创造性地提高 MIP 在分子分析中的性能。