Table 1.
Recent studies on HBV detection.
Target | Materials/Sensing Strategy | Detection limit (limit of detection) | Time | Advantages | Limitations | Reference Number |
---|---|---|---|---|---|---|
HBV-DNA | Paper based electrochemical platform/Electrochemical | 85 pM | 5 min | Cost-effective, easy fabrication | Require Electrochemical Instrument | [32] |
HBV-DNA | cationic polythiophene/Optical | 1nM- 10 μM (600 pM) | 45 min | paper-based assay, cost-effective | sensitivity issue in undiluted plasma | [33] |
HBV-DNA | Micro-Scale chip based PCR | 100-1000 copies/μL (278copies/μL) | NA | Low sample volume | solution based assay, tedious sample preparation |
[34] |
HBV-DNA | Streptavidin-coated gold nanoparticles/Optical | 0.01 pM | NA | Very low detection limit | Not cost effective Tedious fabrication steps |
[35] |
HBsAg | Gold coated slides/Surface Plasmon Resonance | 0.002–1 U/mL | 10 min | Label Free | Require Optical instrument | [36] |
HBV-DNA | Copper nanocluster/Optical | 20 fmol | NA | Very low detection limit | Require Optical instrument | [37] |
HCV RNA | Gold nanoparticles/Optical | 4.6 U/μL | 30 min | Direct forward Colorimetric detection | Not cost effective Tedious fabrication steps |
[38] |
HBV-DNA | cationic polythiophene impregnated cartridge | 1nM-1μM | 30 min | Cartridge-based assay, no external equipment for sample preparation | sensitivity issue in undiluted plasma | Present work |