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10.1021/acs.analchem.1c01950

http://scihub22266oqcxt.onion/10.1021/acs.analchem.1c01950
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34338520!ä!34338520

suck abstract from ncbi


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pmid34338520      Anal+Chem 2021 ; 93 (32): 11225-11232
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  • Multiplexed Magnetofluorescent Bioplatform for the Sensitive Detection of SARS-CoV-2 Viral RNA without Nucleic Acid Amplification #MMPMID34338520
  • Zayani R; Rezig D; Fares W; Marrakchi M; Essafi M; Raouafi N
  • Anal Chem 2021[Aug]; 93 (32): 11225-11232 PMID34338520show ga
  • Rapid and sensitive detection of SARS-CoV-2 virus genetic material is of paramount importance to mitigate the COVID-19 pandemic outbreak and lower the death toll. Herein, we report the design of a magnetofluorescent bioplatform for the direct and specific detection of the viral RNA of SARS-CoV-2 in the total RNA extracted from nasopharyngeal swabs of COVID-19-positive patients. A higher fluorescence response was achieved using two capture probes tethered to magnetic beads using a biotin/streptavidin linkage, targeting two specific sites in the ORF1a and S genes. Two horseradish peroxidase (HRP)-conjugated reporter sequences, complementary to the loci of the S and N genes, were used to reveal the presence of the viral RNA through the oxidation of o-phenylenediamine to fluorescent 2,3-diaminophenazine. Under optimal conditions, the bioplatform showed high selectivity and sensitivity and was able to detect as low as 0.01 ng of viral RNA (1 x 10(3) copies/muL) with a linear dynamic range varying from 0.01 to 3.0 ng (1 x 10(3) to 9 x 10(7) copies/muL). The bioplatform was also able to discriminate the SARS-CoV-2 RNA from those of other related viruses such as hepatitis C, West Nile, measles, and non-polio viruses. Furthermore, the developed biosensor was validated in 46 clinical samples (36 COVID-19-positive patients and 10 COVID-19-negative subjects, as assessed with the gold standard RT-qPCR method). Both sensitivity and specificity of the developed method reached 100%. Finally, making such a simple and specific method available in the field, at a primary point of care, can better help the detection of SARS-CoV-2 infection in low-resource settings.
  • |*COVID-19[MESH]
  • |*RNA, Viral/genetics[MESH]
  • |Humans[MESH]
  • |Nucleic Acid Amplification Techniques[MESH]
  • |Pandemics[MESH]
  • |SARS-CoV-2[MESH]


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