An electrochemical aptasensor based on Ce-MOF@COF to detect carcinoembryonic antigen

被引:5
|
作者
Li, Shurui [1 ]
Cao, Tianzi [1 ]
Zhang, Han [1 ]
Sun, Yuanling [1 ]
Luo, Chuannan [1 ]
机构
[1] Univ Jinan, Key Lab Interfacial React & Sensing Anal Univ Shan, Sch Chem & Chem Engn, Jinan 250022, Peoples R China
基金
中国博士后科学基金;
关键词
Molybdenum disulfide;
D O I
10.1039/d4nj01743a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, a gold-supported cerium-based organic framework hybrid structure (Au@Ce-MOF@COF) and gold@molybdenum disulfide@graphene oxide (Au@MoS2@rGO) were successfully prepared, and used for constructing an electrochemical aptasensor to detect carcinoembryonic antigen (CEA). Au@MoS2@rGO has a large surface area and good electron transfer rate, so it was used as the substrate to immobilize more aptamers (Apt1). The prepared Ce-MOF@COF was also used as a substrate for the immobilization of aptamers (Apt2) and horseradish peroxidase (HRP). When CEA exists, CEA binds to Au@Ce-MOF@COF-HRP-Apt2. In the presence of H2O2, it can effectively promote the oxidation of hydroquinone (HQ) to benzoquinone (BQ), and the electrochemical reduction signal of BQ was significantly amplified. So, the highly sensitive and selective detection of CEA was achieved. The linear range of the aptasensor is 0.1 pg mL-1-100 ng mL-1, and the detection limit is 0.019 pg mL-1, which shows excellent selectivity, reproducibility and stability. Finally, the aptasensor was applied to detect CEA in serum. In the presence of H2O2, Au@Ce-MOF@COF-HRP can effectively promote the oxidation of hydroquinone (HQ) to benzoquinone (BQ), and the electrochemical reduction signal of BQ was significantly amplified.
引用
收藏
页码:10628 / 10635
页数:8
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