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. 2020 Jul 3;20(13):3728. doi: 10.3390/s20133728

Table 3.

Comparison of the Sensing Properties of Different Genosensors for the Detection of DENV.

Sensing Interface Method/Target Dynamic Range LOD Ref.
pDNA2-liposome/biotin-pDNA1-SMB Fluorescence/synthetic DNA and RNA amplicon 0.125 nM–50 pM 0.125 nM [39]
SH-pDNA-AuNP QCM/PCR 130mtDNA amplicon 2 × 100–2 × 106 PFU/mL 2 PFU/mL [40]
pDNA/IEM I-V curve/RT-PCR DNA amplicon -- 0.17 aM [41]
NH2-pDNA/APS/Pt/AAO EIS or DPV/synthetic 30mtDNA 1 pM–1 μM 2.7 pM [15]
pDNA/PGE DPV/synthetic 22mtDNA 10–100 nM 3.1 nM [18]
NH2-pDNA/chitosan/ZnO/Pt-Pd/FTO CV/synthetic 35mtDNA 1–100 μM 43 μM [19]
NH2-pDNA/MPA/Mn2O3 nanofiber/GCE EIS or DPV/synthetic consensus dengue primer 1 aM–1 μM 0.12 aM [20]
ITO LSV/pDNA-RNA amplicon mixture -- 2 amol [26]
pDNA/SiO2@APTES-GO/Pt EIS/extracted RNA -- 1 fM [16]
NH2-pDNA/MHA/MCH/Au EIS/extracted RNA 102–105 PFU/mL 20 PFU/mL (~20 aM) This work

AAO: anodic aluminum oxide, APS: 3-aminopropyltrimethoxysilane, DPV: differential pulse voltammetry, FTO: fluorine doped tin oxide, IEM: ion-exchang nanomembrane sensor, I-V: current-voltage, LSV: linear sweep voltammetry, SMB: streptavidin magnetic bead, MPA: mercaptopropionic acid, PGE: pencil graphite electrode, QCM: quartz crystal microbalance, SPR: surface plasmon resonance, LOD: limit of detection.