Table 15.1.
Nanosensors Used for Detection of Pathogens
| Analyte | Nanomaterial | Detection Method | Detection Limits | References |
|---|---|---|---|---|
| Bacilli | ||||
| Campylobacter jejuni | Lectin immobilized on gold surface of quartz crystal electrode | QCM | Reusable, limit of detection 103 cells within 30 min | Safina et al. (2008) |
| E. coli O157:H7 | Core-shell Cu/AuNPs with anti-E. coli Ab | Anodic-stripping voltammetry | Detection limit is 30 CFU/mL within a time span of 2 h | Zhang et al. (2009) |
| Magnetic nanobeads | Impedance spectroscopy | 45 log CFU/g in freshly ground beef, assay time 35 min | Varshney et al. (2005) | |
| Ab immobilized gold-coated on QCM | QCM with dissipation monitoring | Log–log linear working range 107–109 cells/mL | Poitras and Tufenkji (2009) | |
| Anti-E.coli Ab immobilized on PEG alkanethiol monolayers on SPR | Sandwich assay SPR immunosensor | Detection limit 106 CFU/mL, highly specific against Salmonella enteritidis | Subramanian et al. (2006) | |
| Sugar attached to iron-oxide NPs | Fluorescent staining | Can isolate up to 88% of E. coli within 45 min | El-Boubbou et al. (2007) | |
| Ab coated on iron-oxide NPs | Optic detection using FTIR/portable mid-IR | 104–105 CFU/mL in 2% milk and spinach extract | Ravindranath et al. (2009) | |
| S. aureus, Vibrio parahaemolyticus, and S. typhimurium | Multicolor upconversion NPs (rare-earth ions) coupled with aptamers attached to magnetic NPs | Magnetic NPs used for immuneseparation with aptamers followed by visible luminescence | 25 CFU/mL for S. aureus 10 CFU/mL for V. parahaemolyticus 15 CFU/mL for S. typhimurium |
Wu et al. (2014) |
| S. typhimurium and S. aureus | AuNPs labeled with Raman reporter molecules | Raman scattering | 103 CFU/mL in spinach wash and peanut butter emulsion | Zhuyi et al. (2011) |
| S. typhimurium | Protein G-coated 11-mercaptoundecanoic acid monolayer on gold surface | SPR | 102–109 CFU/mL | Oh et al. (2004) |
|
S. typhimurium, Shigella flexneri, and E. coli O157:H7 |
Combination of magnetic NPs and Ab-conjugated semiconductor QD | Magnetic NPs immobilized with Ab and quantified by fluorescence | 10–3 CFU/mL within 2 h in food matrix protein in high concentration decreased sensitivity of the method | Zhao et al. (2009) |
| Salmonella | Anti-Salmonella Ab immobilized to QD | Fluorescence at 415 nm UV | 4 × 103 CFU/mL in food extracts | Kim et al. (2013) |
| S. aureus | AuNPs immobilized with anti-S. aureus Ab | Magnetic beads enhance capture of S. aureus from milk matrix florescence of gold quantified | Assay time 40 min, low sensitivity with detection limit of 5 log CFU/mL | Sung et al. (2013) |
| Viruses | ||||
| Cauliflower mosaic virus | Lead sulfide NPs linked to cauliflower mosaic virus 35S oligonucleotide | Sensitive differential pulse anodic stripping voltammetric | Detection limit was 4.38 × 10–12 M/L | Sun et al. (2008) |
| Tomato ring-spot virus and grapevine fan leaf virus | Mesoporous silicon | Change in electric parameters after adsorption | Effective virus size for detection was 50 nm | Vashpanov et al. (2008) |
| Spores | ||||
| Bacillus anthracis spores | Polyaniline-coated magnetic NPs (100 nm) | Detection mechanism depend on capillary flow of captured spores | Limit of detection 4.2 × 102 spores/mL within 16 min | Pal and Alocilja (2009) |
| Bacillus thuringiensis spores | 60-base aptamer conjugated to zinc-sulfide capped CdSe QD | Detects at 655 nm with no photo bleaching of QDs | Semiquantitative, specific and detects 1000 CFU/mL | Ikanovic et al. (2007) |