Sun Xiaolu, Jian Yannan, Wang He, Ge Shenguang, Yan Mei, Yu Jinghua
Shandong Collaborative Innovation Center of Technology and Equipements for Biological Diagnosis and Therapy, Institute for Advanced Interdisciplinary Research , University of Jinan , Jinan 250022 , P.R. China.
School of Chemistry and Chemical Engineering , University of Jinan , Jinan 250022 , P.R. China.
ACS Appl Mater Interfaces. 2019 May 1;11(17):16198-16206. doi: 10.1021/acsami.9b02005. Epub 2019 Apr 17.
In this work, we proposed a strategy that combined molecularly imprinted polymers (MIPs) and hybridization chain reaction into microfluidic paper-based analytical devices for ultrasensitive detection of target glycoprotein ovalbumin (OVA). During the fabrication, Au nanorods with a large surface area and superior conductibility were grown on paper cellulosic fiber as a matrix to introduce a boronate affinity sandwich assay. The composite of MIPs including 4-mercaptophenylboronic acid (MPBA) was able to capture target glycoprotein OVA. SiO@Au nanocomposites labeled MPBA and cerium dioxide (CeO)-modified nicked DNA double-strand polymers (SiO@Au/dsDNA/CeO) as a signal tag were captured into the surface of the electrode in the presence of OVA. An electrochemical signal was generated by using nanoceria as redox-active catalytic amplifiers in the presence of 1-naphthol in electrochemical assays. As a result, the electrochemical assay was fabricated and could be applied in the detection of OVA in the wide linear range of 1 pg/mL to 1000 ng/mL with a relatively low detection limit of 0.87 pg/mL (S/N = 3). The results indicated that the proposed platform possessed potential applications in clinical diagnosis and other related fields.
在本研究中,我们提出了一种将分子印迹聚合物(MIPs)与杂交链式反应相结合的策略,用于在基于微流控纸的分析装置中对目标糖蛋白卵清蛋白(OVA)进行超灵敏检测。在制备过程中,具有大表面积和优异导电性的金纳米棒生长在纸质纤维素纤维上作为基质,以引入硼酸亲和夹心分析。包含4-巯基苯硼酸(MPBA)的MIPs复合物能够捕获目标糖蛋白OVA。在OVA存在的情况下,标记有MPBA的SiO@Au纳米复合材料和作为信号标签的二氧化铈(CeO)修饰的带切口DNA双链聚合物(SiO@Au/dsDNA/CeO)被捕获到电极表面。在电化学分析中,在1-萘酚存在的情况下,使用纳米氧化铈作为氧化还原活性催化放大器产生电化学信号。结果,构建了电化学分析方法,该方法可用于在1 pg/mL至1000 ng/mL的宽线性范围内检测OVA,检测限相对较低,为0.87 pg/mL(S/N = 3)。结果表明,所提出的平台在临床诊断和其他相关领域具有潜在应用。