Table 2.
Methods | Biomarker | Limit of detection | Time-to-result | Sample preparation | Portability | Scale | Use cases | References |
---|---|---|---|---|---|---|---|---|
CDC RT-PCR diagnostic panel | SARS-CoV-2 RNA | 100 copies/µL | 3 h | Complex | Unportable | Low throughput | ID/AIS/ES | CDC Instruction Manual: CDC-006-00019, Revision: 0311 |
Magnetic | ||||||||
Magnetic NP capture | SARS-CoV-2 viral RNA | 10 copies | 30 min (extraction) | Simple | Unportable | Low throughput | ID/AIS/ES | Zhao et all90 (not peer reviewed) |
Self-assemble magnetic nanoparticles | Adenovirus-5 and Herpes simplex virus-1 antigen | 5 viral particles/10 µL | <30 min | Simple | Unportable | High throughput | ID/AIS | Perez et al50 |
Fluorescent-magnetic-catalytic nanospheres | H9N2 avian influenza virus antigen | 10 pg/mL (electrical) and 69.8 ng/mL (fluorescence) | 1–2 h | Simple | Portable | Low throughput | ID | Peng et al49 |
Optical | ||||||||
Catalytic colorimetric reagent | Anti-SARS-CoV-2 antibodies | N/A | Within 15 min | Simple | Portable | Low throughput | ID | Zhengtu et al35 |
Fluorescently labeled biosensor | SARS-CoV-2 Antibody | N/A | 10 min | Simple | Portable | High throughput capable | ID | Zhenhua et al13 |
Functionalized QD | Respiratory syncytial virus antigen | N/A | 6 days (plaques) | Complex | Unportable | Low throughput | ID | Tripp et al71 |
Liposome-quantum dot complexes | HIV DNA | 0.1 fM | <1 hour | Complex | Unportable | Moderate throughput | ID/AIS | Zhou et al91 |
PDA liposomes | Influenza antigen | 11 HAUs | <1 hour | Simple | Portable | Moderate throughput | ID | Riechert et al55 |
RT-LAMP pH-based colorimetric sensor | ZIKV RNA | 1 copy/uL | 10 min | Complex | Portable | Moderate throughput | ID/AIS | Kaarj et al28 |
Plasmonic | ||||||||
Surface plasma | SARS-CoV-2 RNA | 0.22 pM | Within 15 min | Simple | Unportable | High throughput capable | ID | Guangyu et al53 |
Plasmonics nanoprobe | HIV-1 DNA | 0.5 μM | 10 s (detection) | Complex | Unportable | High throughput capable | ID | Wabuyele et al76 |
SPR SERS | HBV DNA | 50 aM | <1 h | Complex | Portable | High throughput capable | ID/AIS/ES | Li et al34 |
Electrochemical sensor | ||||||||
Field-effect transistor | SARS-CoV-2 antigen | 2.42 × 102 copies/mL | 30 s | Simple | Portable | Low throughput | ID/AIS/ES | Seo et al58 |
Potentiostat sensor | SARS-CoV-2 antigen | 10 fM | 10–30 s | Simple | Portable | Moderate throughput | ID/AIS | Mahari et al38 (not peer reviewed) |
Screen-printed carbon electrodes | SARS DNA | 2.5 pM | 20 min | Complex | Portable | Moderate throughput | ID | Martínez-Paredes et al41 |
Nanoparticle-streptavidin conjugates | HBV DNA | 2.0 pM | N/A | Complex | Unportable | High throughput capable | ID | Wang et al 79 |
AgNPs modified carbon electrode | Influenza antigen | sub pM | 15 min | Simple | Unportable | Moderate throughput | ID/AIS | Sepunaru et al 59 |
Lateral flow immunoassay | ||||||||
Lanthanide-doped nanoparticles | SARS-CoV-2 antibody | 1:1000 dilution | 10 min | Complex | Portable | Moderate throughput | ID | Chen et al13 |
Raman scattering | Influenza A H1N1 virus and HAdV | 50 pfu/mL (HAdV)and 10 pfu/mL (H1N1) | 30 min | Simple | Unportable | High throughput capable | ID | Wang et al80 |
Technologies specific for SARS-CoV-2 in bold. Methods which can directly applied the collected sample from patients are termed “Simple”. Methods requiring extra sample processing steps are regarded as “Complex”. Devices that can only process one sample per time are defined as low throughput. Devices that have potential to process multiple samples per time, even if their ability is not mentioned in original papers, are termed “High throughput capable”
We have split the technologies into use cases based upon limit of detection requirements— ID infection diagnosis, AIS asymptomatic screening, and ES environmental surveillance