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A novel smartphone-integrated binary-emission molecularly imprinted fluorescence sensor embedded with MIL-101(Cr) for sensitive and real-time detection of protein

化学 检出限 碲化镉光电 荧光 分子印迹聚合物 纳米传感器 分析化学(期刊) 色谱法 纳米技术 选择性 催化作用 生物化学 物理 材料科学 量子力学
作者
Wei Hu,Shasha Feng,Fubin Pei,Bin Du,Bing Liu,Xihui Mu,Zhaoyang Tong
出处
期刊:Talanta [Elsevier BV]
卷期号:260: 124563-124563 被引量:6
标识
DOI:10.1016/j.talanta.2023.124563
摘要

Aiming for precise, real-time, and on-site analysis of proteins, an innovative binary-emission fluorescence imprinted polymer was designed by sol-gel method after mixing MIL-101(Cr), green CdTe (g-CdTe) and red CdTe (r-CdTe) for detection of protein. In this proposal, MIL-101(Cr), as a favorable supporter, provided high surface area and porosity for imprinting sites, which ameliorated the transfer rate and the sensitivity of the nanosensor. And g-CdTe and r-CdTe were served as signal transduction for dual-emission response. Based on strengthened recognition reaction between high-affinity imprinting sites and protein, the fluorescence intensities of g-CdTe and r-CdTe yielded conspicuous two responses at 528 nm and 634 nm for protein under the excitation of 350 nm. The cytochrome c (Cyt c) and trypsin were served as model proteins to verify the generality of strategy. Given prominent merits of MIL-101(Cr), g-CdTe/r-CdTe@MIL-101(Cr)@MIP exhibited good linear range of 1-30 μM for Cyt c and 0.15-4 μM for trypsin, and the limit of detection were 0.13 μM and 0.014 μM, respectively. Significantly, an unsophisticated smartphone-based sensing device was developed by integrating g-CdTe/r-CdTe@MIL-101(Cr)@MIP with a 3D printing portable device to obtain precise on-site results. As expected, this portable platform was successfully applied for monitoring Cyt c and trypsin with a detection limit of 0.71 μM and 0.026 μM, respectively. These results indicated this dual-response molecularly imprinted fluorescence senor based on smartphone provided promising perspectives on futural on-site protein analysis.
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