| Literature DB >> 26762619 |
Sheikh M Talha1, Teppo Salminen2, Etvi Juntunen2, Anni Spangar2, Chandrasekhar Gurramkonda3, Tytti Vuorinen4, Navin Khanna5, Kim Pettersson2.
Abstract
Hepatitis B infection, caused by hepatitis B virus (HBV), presents a huge global health burden. Serological diagnosis of HBV mainly relies on the detection of hepatitis B surface antigen (HBsAg). Although there are high sensitivity commercial HBsAg enzyme immunoassays (EIAs) available, many low-resource laboratories lacking trained technicians continue to use rapid point-of-care assays with low sensitivities for HBsAg detection, due to their simplicity to operate. We developed a time-resolved fluorometric dry-reagent HBsAg immunoassay which meets the detection limit of high sensitivity EIAs but is simple to operate. To develop the assay, anti-HBsAg monoclonal antibody coated on europium nanoparticles was dried atop of biotinylated anti-HBsAg polyclonal antibody immobilized on streptavidin-coated microtiter wells. To test a sample in dry-reagent assay, serum sample and assay buffer were added to the wells, incubated, washed and europium signals were measured. The assay showed a detection limit of 0.25 ng/ml using HBsAg spiked in serum sample. When evaluated with 24 HBV positive and 37 negative serum samples, assay showed 100% sensitivity and specificity. Assay wells are stable for at least 26 weeks when stored at 4°C, and can tolerate elevated temperatures of up to 35°C for two weeks. The developed assay has high potential to be used in low-resource laboratories.Entities:
Keywords: Assay; Diagnostics; Europium; HBsAg; Hepatitis B virus; Time-resolved
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Year: 2016 PMID: 26762619 DOI: 10.1016/j.jviromet.2016.01.001
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014