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BioMK | Diseases | Procedure | NPs used | LoD | Reference |
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Viral diseases |
Antibodies against COVID-19 | COVID-19 | Multiplexed grating-coupled FRS plasmonics | Au-coated nanoscale | 1 : 1600 dilution | [106] |
Dengue viral RNA | Dengue virus | ETC monitoring | Methylene blue conjugated AuNPs | 100.00 fM | [107] |
S spike glycoproteins | SARS-CoV-2 | ETC monitoring | GPO and Au nanostars | | [108] |
Peptide DNA/RNA | Influenza A viruses (H1 to H16 subtypes) | Visual colorimetric assay (CMA) | Au NPs | 2.30 ng | [109] |
DENV proteins | Dengue viral disease | ELISA-plate spectrophotometers | Au nanorods | 1.00 pg | [110] |
COVID-19 spike protein | COVID-19 | FET-based BioSS | GP sheets | | [111] |
Complementary sequences of RdRp-COVID-19, ORF1ab-COVID-19, and E genes of COVID-19 | COVID-19 | PPT effect and LSPR sensing transduction | Dual-dimensional Au nanoislands (AuNIs) | 0.22 pM | [112] |
HBV DNA | Hepatitis B | ETC impedance spectra (EIS) | Tin-doped WO3/In2O3 nanowires | 0.10 pM to 10.00 μM | [113] |
Virus DNA/RNA | Narrowly related Zika and dengue viruses | Fluorometric detection | GPO | | [114] |
Dengue viral DNA | Dengue viral disease | Sandwich hybridization strategy of DNAs | AuNPs | | [111] |
Sialyl oligosaccharide receptor-mimic peptide | Influenza A virus | Optimized peptide termination | Boron-doped diamond electrode | 5.00–10.00 pfu/sample | [115] |
HCVcoreAg | Hepatitis C | Modification of buffer pH from acidic to neutral | Silicon-on-insulator (SOI) nanowire | 0.30 pg/mL | [116] |
Concanavalin A lectin | Dengue type 2, Zika, chikungunya, and yellow fever | Cyclic VTM and impedance spectroscopy | Zinc oxide NPs | 0.0421 pfu/mL for ZIKV, 0.0437 pfu/mL for YFV, 0.062 pfu/mL for CHIKV, and 0.0382 pfu/mL for DENV | [117] |
L-lysine levels | HIV | APM BioSS | L-lysine oxidase (LOx NPs) and GPO NPs | 0.01 μM | [113] |
Nonspecific proteins | MERS-CoV and HCoV | Electrochemiluminescence | Au NPs | 0.40 and 1.00 pg mL−1 for HCoV and MERS-CoV, respectively | [118] |
Hepatitis B virus gene | Hepatitis B | ETC monitoring | AMT-Au NPs-PGEs | 0.86 μg/mL | [119] |
Viral DNA | HPV-18 | FRS assay | Ti3C2 nanosheets | 100.00 pM | [120] |
HIV-1 gene | AIDS | Electrochemiluminescence NanoBioSS | Europium sulfide nanocrystals (EsNCs) | 3.00 fM to 0.30 nM | [121] |
Envelop protein AB (Zev-Abs) | Zika virus | ETC IMSS | Interdigitated microelectrode of Au (IDE-Au) | 10.00 pM | [122] |
Virus oligonucleotide | MERS-CoV | CMA | Citrate anion-stabilized AgNPs | 1.53 nM | [123] |
Virus oligonucleotide | Human papillomavirus | CMA | Citrate anion-stabilized Ag NPs | 1.03 nM |
Surface receptor | Influenza A | Chromatographic assay | Carbon NPs | 350 TCID50/mL (i.e., the 50% tissue culture infectious dose) | [124] |
JEV via recognition cavities | Japanese encephalitis virus | FRS detection | Magnetic silicon microspheres | 2.50–45.00 nM | [125] |
| Influenza A (H1N1) and A (H3N2) | Paper-based immunoassay (IMA) | Au NPs | plaque-forming unit per assay | [126] |
AB specific to influenza virus | Influenza A (H7N9) | ETC sensor | GPO, multiwalled CN | 0.81 pg/mL | [127] |
AB specific to viral infection | Influenza A and B | IMA | Europium NPs | to EID 50/mL | [128] |
Specific mouse α-A NP mAbs | Influenza A (H1N1) | FRS IMA | Magnetic NPs (MnFe2O4) | 0.007 HAU | [129] |
| Influenza A (H3N2) | FET BioSS | Silicon nanowire, magnetic NPs | 29 viruses/μL | [130] |
DNA-based detection | Influenza A (H5N1) | DNA-based microarray assay (scanometric detection) | AuNPs with Ag staining technique | per assay (PCR fragments) TCID50 per assay (viral RNA) | [131] |
|
Bacterial diseases |
Bacterial target DNA | S. aureus | Targeted DNA was quantified in spectrophotometry at 260 nm; the sensitivity of this method was studied with PCR and gel agarose electrophoresis | MNP-TiO2-AP-SMCC | 230.00 CFU/mL | [132] |
Electrostatic interaction of cell wall and concomitant inhibition of peroxidase activity of CS-MNPs | Gram-negative Escherichia coli or the Gram-positive Staphylococcus aureus | CMA | Chitosan-coated iron oxide magnetic NPs (CS-M NPs) | by the naked eye and by spectrophotometry within 10 min | [133] |
Anti-E. coli O157 AB | E. coli O157 | Cyclic VTM and ETC impedance spectroscopy | Au NPs | 15.00 CFU/mL | [134] |
Anti-E. coli AB | E. coli | Chemiresistive BioSS | Au NPs | 12.00 CFU/mL | [135] |
Biofilm | Staphylococcus epidermidis | ETC sensing | Magnesium zinc oxide (MZO) NS | A drain current change of ~80% after ~200 min of S. epidermidis bacteria culturing | [136] |
Bacterial peptides | Listeria monocytogenes and Staphylococcus aureus | ETC BioSS | Au NPs | 3.00 CFU/mL for Staphylococcus aureus and 9.00 CFU/mL for Listeria monocytogenes | [137] |
Bacteria’s target DNA | Foodborne bacteria including Escherichia coli O157:H7, Vibrio parahaemolyticus, Salmonella, Staphylococcus aureus, Listeria monocytogenes, Shigella, etc. | Amplified microcantilever array BioSS | Au NPs | 0.005–0.040 fM or 1–9 cells/mL | [138] |
Receptor-binding protein of bacteria | Escherichia coli, Pseudomonas aeruginosa, and Vibrio cholerae | CMA | Au NPs | ∼100 cells | [139] |
Mycobacterium tuberculosis oligonucleotide | Mycobacterium tuberculosis (MTB) | CMA | Citrate anion-stabilized (Ag NPs) | 1.27 nM | [123] |
Fungal diseases |
Fungal spores | Aspergillus niger | CMA | Peptide-modified Au NPs | 50 spores | [140] |
Concanavalin A (ConA) and wheat germ agglutinin (WGA) lectins | Candida spp. | Impedimetric BioSS | Lectin-modified Au NPs | | [141] |
Protein BioMK | Aspergillus fumigatus allergen Asp f 1 | CMA | Magneto-BioSS biochip | ~100.00 pg/mL | [142] |
|
Parasitic diseases |
AB as receptor | Malaria | ETC BioSS | Platinum NPs (Pt NPs) | 8.00 ng/mL | [143] |
pLDH | Malaria | EIS: ETC impedance spectroscopy | GCE | 0.50 fM | [144] |
β-Hematin | P. berghei, P. falciparum | ETC NS | Au-CuO | 3.60–4.80 mM 0.65–1.35 mM | [145] |
Bilharzia AB | Bilharzia disease | ETC NanoBioSS | Nanostrip with immobilized Au NPs | | [146] |
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