AI Article Synopsis

  • Viral infections remain a significant health challenge, and traditional RT-PCR methods for virus detection are reliable but lengthy and complex.
  • A new direct detection method for the CoV-2 genome using fluorescein-loaded mesoporous silica nanoparticles provides a faster alternative, eliminating the need for extensive processing.
  • This method showed promising results, with a detection time of just 15 minutes and good sensitivity (84%) when tested on clinical samples.

Article Abstract

Viral infection has been one of the major health issues for human life. The real-time reverse transcription polymerase chain reaction (RT-PCR)-based detection has primarily been used for virus detection as a highly reliable procedure. However, it is a relatively long and multi-stage process. In addition, required skilled personnel and complex instrumentation presents difficulties in large scale monitoring efforts. Therefore, we report here a direct and fast detection method for CoV-2 genome as applied in the nose-throat swab samples without any further processing. The detection principle is based on fluorescein-loaded mesoporous silica nanoparticles capped by specific gene sequences probes immobilized on the surface of the nanoparticles. Upon hybridization with the target viral genome, the fluorescein molecules were released from the mesopores. Testing with synthetic oligonucleotides, the NSP12 gene-based detection resulted in a strong signal. Target detection time could be optimized to 15 min and the limit of detection was 1.4 RFU with 84% sensitivity with clinical samples (n = 43).

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Source
http://dx.doi.org/10.1016/j.talanta.2022.123429DOI Listing

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