Table 7.
Summary of herpes viruses' DNA biosensor.
Virus | Genosensor type | Method | Electrode | Assay time | Linear rang | Detection limit | Ref |
---|---|---|---|---|---|---|---|
HSV I | Piezoelectric | Acoustic | QCM | 3 min | 5.2 × 10−11_1.3 × 10−7 M | 10−18 M | [254] |
HSV I | Piezoelectric | Acoustic | Gold | 6 min | _ | 5.2 × 10−12 M | [255] |
HSV I | Capacitive | Impedimetric | Aluminum | 30 s | _ | 21 × 10 −17 M | [256] |
CMV | Electrochemical | Voltammetric | SPE | _ | 1 × 10−10M | 6 × 10 −16M | [257] |
CMV | Electrochemical | Amperometric | SPE | _ | 3 × 10 −8_ 2 × 10−7 M | 3 × 10 −11 M | [258] |
CMV | Optical | Fluorometric | GO | _ | _ | 4.15 × 105IFU/ml | [259] |
CMV | Optical | SPR | Gold | <1 h | _ | 24_108 × 10 −15M | [260] |
CMV | Piezoelectric | PCR | QCM | _ | 0_500 × 10 −9 M | 25 × 10 −9 M | [261] |
CMV | Piezoelectric | SDA | Gold | >3 h | _ | _ | [262] |
EBV | Electrochemical | Voltammetric | Graphite | _ | 3.78_756 × 10 −6 M | 17.32 × 10 −9 M | [263] |
EBV | Electrochemical | Microfluidic | Gold | 10 min | 1.0 × 103_1.0 × 10−1 copies/mL | 1.1 × 103 copies/mL | [264] |
EBV | Electrochemical | EIS | Gold | _ | 1 × 10−15_1 × 10−9 M | 38 × 10−17 M | [265] |
EBV | LF | LF | Gold | _ | _ | _ | [266] |
EBV | Electrochemical | Signal amplification | QCM-D | _ | 11.235 × 10−11 _2.247 × 10−9 M | 112.35 × 10−12M | [267] |
HHV-5 | Electrochemical | Voltammetric | Zn–Ag | 5 s | 113_103 and 3 × 105_106copies/mL | 97 copies/mL | [268] |
KSHV | LF | SERS | Gold | 20 min | 0_100 × 10 −12 M | 0.043 × 10 −12 M | [269] |
SPE; screen-printed carbon electrode, IFU; immunofluorescence focus unit, SPR; surface plasmon resonance, GO; graphene oxide, SDA; strand displacement amplification, EIS; electrochemical impedance spectroscopy, LF; lateral flow, QCM-D; quartz crystal microbalance with a dissipation monitoring, Zn–Ag; zinc-silver, SERS; surface-enhanced Raman scattering.