4.8 Article

In situ enzymatic silver enhancement based on functionalized graphene oxide and layer-by-layer assembled gold nanoparticles for ultrasensitive detection of thrombin

期刊

BIOSENSORS & BIOELECTRONICS
卷 38, 期 1, 页码 50-54

出版社

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2012.04.046

关键词

Graphene oxide; Alkaline phosphatase; Gold nanoparticles; Silver enhancement; Thrombin; Layer-by-layer assembly; Aptasensor

资金

  1. National Natural Science Foundation of China [21075100]
  2. Ministry of Education of China [708073]
  3. Specialized Research Fund for the Doctoral Program of Higher Education [20100182110015]
  4. Fundamental Research Funds for the Central Universities [XDJK2012A004]
  5. State Key Laboratory of Electroanalytical Chemistry [SKLEAC 2010009]
  6. Natural Science Foundation Project of Chongqing City [CSTC-2011BA7003, CSTC-2009BA1003]

向作者/读者索取更多资源

A highly specific in situ amplification strategy was designed for ultrasensitive detection of thrombin by combining the layer-by-layer (LBL) assembled amplification with alkaline phosphatase (ALP) and gold nanoparticles (Au) mediated silver deposition. High-density carboxyl functionalized graphene oxide (FGO) was introduced as a nanocarrier for LBL assembling of alkaline phosphatase decorated gold nanoparticles (ALP-Au), which was further adopted to label thrombin aptamer II. After sandwich-type reaction, numerous ALP were captured onto the aptasensor surface and catalyzed the hydrolysis of ascorbic acid 2-phosphate (AAP), which in situ generated ascorbic acid (AA), reducing Ag+ to Ag nanoparticles (AgNPs) for electrochemical readout. Inspiringly, the in situ amplification strategy with ethanolamine as an effective blocking agent showed remarkable amplification efficiency, very little nonspecific adsorption, and low background signal, which was favorable to enhance the sensitivity of aptasensor. Our novel dramatic signal amplification strategy, with a detection limit of 2.7 fM, showed about 2-3 orders of magnitude improvement in the sensitivity for thrombin detection compared to other universal enzyme-based electrochemical assay. (c) 2012 Elsevier B.V. All rights reserved.

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