Sensitive aptasensing of hepatitis B viral antigen gold dielectrode by current-volt measurements

Hepatitis B virus (HBV) is a serious human health issue, primarily leading to cirrhosis, chronic hepatitis, and primary liver cancer. Patients are at higher risk of a poor prognosis if the viral load exceeds >10(5) copies/mL; hence, it is crucial to identify the early stages of HBV infection. Thi...

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Bibliographic Details
Main Authors: Geng, Huijuan, Gopinath, Subash Cb, Chen, Yeng, Niu, Wenyan
Format: Article
Published: Amer Scientific Publishers 2022
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Online Access:http://eprints.um.edu.my/40440/
https://doi.org/10.1166/jno.2022.3288
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Institution: Universiti Malaya
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Summary:Hepatitis B virus (HBV) is a serious human health issue, primarily leading to cirrhosis, chronic hepatitis, and primary liver cancer. Patients are at higher risk of a poor prognosis if the viral load exceeds >10(5) copies/mL; hence, it is crucial to identify the early stages of HBV infection. This research aimed to identify hepatitis B surface antigen (HBsAg) on an interdigitated gold electrode sensor assisted by HBsAg-specific aptamer and antibody interactions. The aptamer-HBsAg-antibody sandwich assay was carried out on an interdigitated electrode using aptamer as the capture molecule and anti-HBsAg antibody as the detection molecule. Higher capture probe immobilization was achieved through the gold nanourchin conjugated capture aptamer. On the aptamer-attached electrode, HBsAg interacted with and was sandwiched by the detection antibody. The sandwich assay lowered the limit of HBsAg detection to 0.1 ng/mL, as indicated by the calculated R-2 value of 0.9915 on a linear regression graph presenting data for concentrations of HBsAg from 0.1 to 60 ng/mL. Furthermore, specific HBsAg detection was confirmed by complementarily of the capture aptamer sequence and nonspecific proteins (hepatitis C-the core antigen (HCVcoreAg) and albumin). A selective experiment revealed a gradual increase in current responses in a HBsAg-spiked serum sample, demonstrating the interference-free detection of HBsAg for the real-life sample.