AI Article Synopsis

  • - The study developed a new quick and cost-effective point-of-care test called STAT-DNA, which uses nanoparticle-DNA aggregation for easy visual detection of the hepatitis C virus (HCV) without complex procedures.
  • - This detection system employs a reverse transcription-polymerase chain reaction (RT-PCR) method with specially labeled primers and aggregates magnetic and polystyrene particles for the visual change needed to confirm HCV presence.
  • - The results from the STAT-DNA test showed a detection limit of at least 10 IU/mL, with no cross-reactivity to other viral pathogens, and were consistent with traditional real-time PCR results from 54 patient samples.

Article Abstract

Rapid, simple, and inexpensive diagnostic point-of-care tests (POCTs) are essential for controlling infectious diseases in resource-limited settings. In this study, we developed a new detection system based on nanoparticle-DNA aggregation (STat aggregation of tagged DNA, STAT-DNA) to yield a visual change that can be easily detected by the naked eye. This simplified optical detection system was applied to detect hepatitis C virus (HCV). Reverse transcription-polymerase chain reaction (RT-PCR) was performed using primers labeled with biotin and digoxigenin. Streptavidin-coated magnetic particles (1 μm) and anti-digoxigenin antibody-coated polystyrene particles (250-350 nm) were added to form aggregates. The limit of detection (LoD) and analytical specificity were analyzed. The STAT-DNA results were compared with those of the standard real-time PCR assay using serum samples from 54 patients with hepatitis C. We achieved visualization of amplified DNA with the naked eye by adding nanoparticles to the PCR mixture without employing centrifugal force, probe addition, incubation, or dilution. The LoD of STAT-DNA was at least 10 IU/mL. STAT-DNA did not show cross-reactivity with eight viral pathogens. The detection using STAT-DNA was consistent with that using standard real-time PCR.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9496050PMC
http://dx.doi.org/10.3390/bios12090744DOI Listing

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