Celiac disease detection using a transglutaminase electrochemical immunosensor fabricated on nanohybrid screen-printed carbon electrodes
Biosensors and Bioelectronics, ISSN: 0956-5663, Vol: 31, Issue: 1, Page: 95-100
2012
- 66Citations
- 61Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations66
- Citation Indexes66
- 66
- CrossRef40
- Captures61
- Readers61
- 61
Article Description
Celiac disease is a gluten-induced autoimmune enteropathy characterized by the presence of tissue tranglutaminase (tTG) autoantibodies. A disposable electrochemical immunosensor (EI) for the detection of IgA and IgG type anti-tTG autoantibodies in real patient's samples is presented. Screen-printed carbon electrodes (SPCE) nanostructurized with carbon nanotubes and gold nanoparticles were used as the transducer surface. This transducer exhibits the excellent characteristics of carbon–metal nanoparticle hybrid conjugation and led to the amplification of the immunological interaction. The immunosensing strategy consisted of the immobilization of tTG on the nanostructured electrode surface followed by the electrochemical detection of the autoantibodies present in the samples using an alkaline phosphatase (AP) labelled anti-human IgA or IgG antibody. The analytical signal was based on the anodic redissolution of enzymatically generated silver by cyclic voltammetry. The results obtained were corroborated with a commercial ELISA kit indicating that the electrochemical immunosensor is a trustful analytical screening tool.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0956566311006658; http://dx.doi.org/10.1016/j.bios.2011.09.044; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84455208295&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/22019096; https://linkinghub.elsevier.com/retrieve/pii/S0956566311006658; https://dx.doi.org/10.1016/j.bios.2011.09.044
Elsevier BV
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