A carboxylated graphene nanodisks/glucose oxidase nanotags and Mn:CdS/TiO2 matrix based dual signal amplification strategy for ultrasensitive photoelectrochemical detection of tumor markers

The Analyst ◽  
2017 ◽  
Vol 142 (24) ◽  
pp. 4647-4654 ◽  
Author(s):  
Jie Song ◽  
Shuo Wu ◽  
Xinlan Yang ◽  
Jingli Yuan

A graphene nanodisk and glucose oxidase based dual signal amplification strategy was developed for a highly sensitive PEC immunoassay of CEA.

RSC Advances ◽  
2020 ◽  
Vol 10 (44) ◽  
pp. 26239-26245
Author(s):  
Yubin Li ◽  
Ling Xie ◽  
Jiaming Yuan ◽  
Huazhong Liu

An assay for Ag+ based on a C–Ag+–C structure by utilizing a HCR/GOx dual-signal amplification strategy and SCGS as an ideal separation material.


2019 ◽  
Vol 55 (56) ◽  
pp. 8076-8078 ◽  
Author(s):  
Huimei Da ◽  
Yaling Liu ◽  
Mengjie Li ◽  
Ruo Yuan ◽  
Hongyan Liu ◽  
...  

We developed a novel “signal-on” photoelectrochemical (PEC) aptasensor with a near-zero background signal by using AgVO3 as a single photoactive material for the sensitive detection of vascular endothelial growth factor (VEGF165).


The Analyst ◽  
2019 ◽  
Vol 144 (5) ◽  
pp. 1671-1678 ◽  
Author(s):  
Xiaoqiang Liu ◽  
Yunfei Tang ◽  
Peipei Liu ◽  
Liwei Yang ◽  
Lele Li ◽  
...  

In this work, a sensitive and selective electrochemical aptasensor for detection of microcystin-LR was developed based on a dual signal amplification system consisted of a novel ternary composite and horseradish peroxidase.


The Analyst ◽  
2020 ◽  
Vol 145 (4) ◽  
pp. 1219-1226 ◽  
Author(s):  
Jingjing Zhang ◽  
Chunyuan Song ◽  
Huiling Zhou ◽  
Juan Jia ◽  
Yinna Dai ◽  
...  

A dual signal amplification strategy comprising target-triggered recycling and DSN-mediated amplifications was designed and proposed for a highly sensitive fluorescence assay of nucleic acids.


Biosensors ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 222
Author(s):  
Chenxin Fang ◽  
Ping Ouyang ◽  
Yuxing Yang ◽  
Yang Qing ◽  
Jialun Han ◽  
...  

A microRNA (miRNA) detection platform composed of a rolling circle amplification (RCA) system and an allosteric deoxyribozyme system is proposed, which can detect miRNA-21 rapidly and efficiently. Padlock probe hybridization with the target miRNA is achieved through complementary base pairing and the padlock probe forms a closed circular template under the action of ligase; this circular template results in RCA. In the presence of DNA polymerase, RCA proceeds and a long chain with numerous repeating units is formed. In the presence of single-stranded DNA (H1 and H2), multi-component nucleic acid enzymes (MNAzymes) are formed that have the ability to cleave substrates. Finally, substrates containing fluorescent and quenching groups and magnesium ions are added to the system to activate the MNAzyme and the substrate cleavage reaction, thus achieving fluorescence intensity amplification. The RCA–MNAzyme system has dual signal amplification and presents a sensing platform that demonstrates broad prospects in the analysis and detection of nucleic acids.


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