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Gold nanoparticle-decorated reduced-graphene oxide targeting anti hepatitis B virus core antigen
Hepatitis B virus core antigen (HBcAg) is the major structural protein of hepatitis B virus (HBV). The presence of anti-HBcAg antibody in a blood serum indicates that a person has been exposed to HBV. This study demonstrated that the immobilization of HBcAg onto the gold nanoparticles-decorated redu...
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Published in: | Bioelectrochemistry (Amsterdam, Netherlands) Netherlands), 2018-08, Vol.122, p.199-205 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Hepatitis B virus core antigen (HBcAg) is the major structural protein of hepatitis B virus (HBV). The presence of anti-HBcAg antibody in a blood serum indicates that a person has been exposed to HBV. This study demonstrated that the immobilization of HBcAg onto the gold nanoparticles-decorated reduced graphene oxide (rGO-en-AuNPs) nanocomposite could be used as an antigen-functionalized surface to sense the presence of anti-HBcAg. The modified rGO-en-AuNPs/HBcAg was then allowed to undergo impedimetric detection of anti-HBcAg with anti-estradiol antibody and bovine serum albumin as the interferences. Upon successful detection of anti-HBcAg in spiked buffer samples, impedimetric detection of the antibody was then further carried out in spiked human serum samples. The electrochemical response showed a linear relationship between electron transfer resistance and the concentration of anti-HBcAg ranging from 3.91ngmL−1 to 125.00ngmL−1 with lowest limit of detection (LOD) of 3.80ngmL−1 at 3σm−1. This established method exhibits potential as a fast and convenient way to detect anti-HBcAg.
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•Protein-functionalized graphene-based nanocomposite to sense anti-HBcAg•Limit of detection of 3.80ngmL−1 in spiked samples•Protein-functionalized electrode is selective and specific towards anti-HBcAg.•Works on diluted human serum sample |
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ISSN: | 1567-5394 1878-562X |
DOI: | 10.1016/j.bioelechem.2018.04.004 |