TABLE I. Nucleic Acid-Based Test.
| Ref. | Substrate / Approach | Detection tools | Detection time | LOD |
|---|---|---|---|---|
| [42] | RT-LAMP | Colorimetry | 1 h | - |
| [102] | One-step RT-LAMP | Colorimetry | 20 min | 80 copies/ml |
| [103] | RT-LAMP | Colorimetry | 20 min | 100 copies/
|
| [104] | One-step RT-LAMP | Colorimetry | 30 min | 1000 copies/ml (5 copies) |
| [105] | RT-LAMP | Colorimetry | 40 min | - |
| [106] | RT-LAMP | Fluorescent | >15 min | 1
101 – 1
102 copies/reaction |
| [107] | RT-LAMP | Colorimetry | 30 min | 102copies |
| [108] | RT-LAMP | Colorimetry, spectrophotometry, and real time fluorescence | >1 h | 59 copies/reaction |
| [109] | RT-LAMP | Colorimetry | 45 min | 200 virions/
|
| [110] | Isothermal rolling circle amplification (RCA) | Portable potentiostat | >2 h | 1 copy/
|
| [17] | Thiol-modified ssDNA-capped AuNPs, paper-based | Simple signal conditioning circuit | >5 min | 6.9 copies/
|
| [111] | Supersandwich-type recognition strategy | EIS | - | 200 copies/ mL (clinics) |
| [47] | CRISPR-based SHERLOCK | Fluorescent and colorimetric readout | >1 hour | 2 aM |
| [46] | Recombinase polymerase amplification (RPA) | LightMix®Modular | - | - |
| [49] | Combined isothermal amplification with CRISPR–Cas12 DETECTR technology | fluorescence-based readout | <40 min | 10 copies per
|
| [102] | One-step RT-LAMP | Colorimetry | 20 min | 80 copies/m |
| [112] | Two-step RT-LAMP | fluorescence-based readout | 25 min | 2 copies per
|
| [44] | RT-LAMP assay on semiconductor technology | Electrochemical | >20min | 10 copies/reaction |
RT-LAMP = reverse transcription loop-mediated isothermal amplification, ssDNA = single-stranded DNA, AuNPs = gold nanoparticles, CRISPR = clustered regularly interspaced short palindromic repeats, SHERLOCK = Specific High Sensitivity Enzymatic Reporter Unlocking, DETECTR = DNA Endonuclease-Targeted CRISPR Trans Reporter.







