4.7 Article

Smartphone-assisted point-of-care testing of nucleic acids based on hybridization chain reaction, magnetic beads, and gold nanorods etching

Journal

SENSORS AND ACTUATORS B-CHEMICAL
Volume 392, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2023.134111

Keywords

Point-of-care testing; Nucleic acids; Hybridization chain reaction; Magnetic beads; Gold nanorods etching; Smartphone-based detection

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This study developed a smartphone-assisted nucleic acid POCT method for rapid and accurate detection of viruses. The method utilized hybridization chain reaction, magnetic beads, and etching of gold nanorods to amplify nucleic acid signal and convert it into a visually semi-quantitative result. The method showed excellent specificity and fast detection time, making it suitable for clinical laboratory diagnosis and nucleic acid POCT research.
Colorimetric biosensors are simple but effective tools that are gaining popularity due to their ability to provide low-cost, rapid, and accurate detection for viruses like the Novel coronavirus, Influenza A, and Dengue virus, especially in point-of-care testing (POCT) and visual detection. In this study, a smartphone-assisted nucleic acid POCT was built using hybridization chain reaction (HCR), magnetic beads (MBs), and oxidized 3,3 & PRIME;,5,5 & PRIME;-tetramethylbenzidine (TMB2+)-mediated etching of gold nanorods (GNRs). The application of HCR without enzyme isothermal characteristics and MBs with easy separation, can quickly amplify nucleic acid signal and remove other reaction components. The blue shift of longitudinal localized surface plasmon resonance (LSPR) based on GNRs showed significant differences in etching color for different concentrations of target nucleic acid, which convert the signal into a visually semi-quantitative colorimetric result, achieving quantitative analysis with the color recognition software built into smartphones. This strategy, which only takes 40 min to detect and is twothirds less time than the PCR, was successfully applied for the detection of the Dengue target sequence with a detection limit of 1.25 nM and exhibited excellent specificity for distinguishing single-base mutations, indicating broad application prospects in clinical laboratory diagnosis and enriching the research of nucleic acid POCT.

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