Clinical evaluation of a novel digital microfluidic based point-of-care test platform for detection of SARS-Cov-2 and influenza A/B.

Clinical evaluation of a novel digital microfluidic based point-of-care test platform for detection of SARS-Cov-2 and influenza A/B.

Publication date: Aug 01, 2024

Respiratory pathogens, such as SARS-CoV-2 and influenza A/B, can cause severe illnesses in susceptible individuals. This research evaluated a novel digital microfluidic point-of-care testing platform designed to detect 23 pathogens, comparing its performance to conventional laboratory-based nucleic acid tests. The platform integrates nucleic acid extraction and amplification processes for rapid detection with only 2 min of hands-on time. Performance assays demonstrated that the platform has high sensitivity (87 %-100 %) and specificity (99 %-100 %) for the detection of the evaluated 3 viruses. Additionally, the platform can be adapted for the detection of other respiratory pathogens, aiding in the early diagnosis of respiratory diseases, identifying the source of an outbreak or epidemic, and curbing the spread of the disease.

Concepts Keywords
Acid COVID-19
Influenza Digital microfluidic platform
Laboratory Humans
Pathogens Influenza A virus
Influenza B virus
Influenza, Human
Microfluidics
Point-of-Care Systems
Point-of-Care Testing
Point-of-care testing
Respiratory pathogens
SARS-CoV-2
SARS-Cov-2
Sensitivity and Specificity

Semantics

Type Source Name
pathway KEGG Influenza A
disease VO time
disease VO Viruses
disease MESH respiratory diseases
disease MESH COVID-19
drug DRUGBANK Influenza A virus
drug DRUGBANK Influenza B virus
disease MESH Influenza Human

Original Article

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