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Sensitive fluorescent sensor for the fuzzy exosomes in serum based on the exosome imprinted polymer sandwiched with aggregation induced emission

适体 微泡 外体 化学 生物物理学 分析物 纳米颗粒 分子印迹聚合物 荧光 分子印迹 纳米技术 材料科学 分子生物学 色谱法 生物 选择性 生物化学 小RNA 基因 催化作用 物理 量子力学
作者
Zerong Liao,Jirun Peng,Chen Shi,Pengjie Zhang,Hui Chen,Dongwei Feng,Tuanjie Zhang,Kaida Ye,Yulin Deng,Yuping Dong,Lina Geng
出处
期刊:Sensors and Actuators B-chemical [Elsevier]
卷期号:358: 131182-131182 被引量:17
标识
DOI:10.1016/j.snb.2021.131182
摘要

Cancer cell derived exosomes are considered as one of the potential biomarkers for the non-invasive cancer diagnosis. Nevertheless, how to efficiently and sensitively detect exosomes is still the biggest obstacle. The not yet well-understood surface of exosomes restricts the application of antibodies or epitope imprinting. In addition, the exosomal detection in serum was challenging. Encouragingly, utilizing the self-assembly property of imprinted polymer technology, little-known intact exosomes was directly used as template here to tail the formation of exosome-binding 3D cavities on the surface of the magnetic particles. Analytes in serum were thus selectively captured by this template eluted imprinted polymer. Furthermore, aptamer mediated aggregation induced emission (AIE) was utilized to selectively “turn-on” ignite the captured targets. The performance of the strategy was evaluated using lysozyme and fuzzy exosomes as targets successively. The linear relationships were obtained between the fluorescence and the concentration of these targets in serum respectively. The recovery rate of lysozyme in serum was 107%. The detection limit (LOD) of exosome in serum was 1.3 × 10 6 particles/mL, lower than the current literature. The discrimination of serum from breast cancer patients and healthy people was also achieved, primarily confirming the reliability of this method. To sum up, a novel “light up” sensor with high sensitivity and selectivity in the real biological fluid was developed by the integration of imprinted polymer (MIP) with heterogenous aptamer mediated AIE signaling. Furthermore, the unique potential of MIPs in unknown target recognition revealed herein provides a bright future in the fuzzy target assay. • Aggregation induced aggregation was used to fluorescent “turn-on” igniting the targets captured by imprinted polymer. • The first imprinted polymer based sensor for exosomes in serum was reported here, whose sensitivity was comparable with ELISA. • The ability of imprinted polymer for the detection of fuzzy or little-known target was revealed.
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