Table 2.
Examples of biosensors based on screen-printed electrodes for the detection of bacteria and evaluation of antibiotic resistance.
| Bacteria/Sample | Sensor Configuration 1 | Analytical Performance | Reference |
|---|---|---|---|
| Electrochemical Impedance Spectroscopy | |||
| S. typhimurium; Cell cultures | SPCE modified with Au NP; aptamer | DL: 600 cfu mL−1; 13.8% increase in RCT for 1 × 105 cfu mL−1 heat-killed bacteria, 100% RCT increase in with live bacteria |
[78] |
| Staphylococcus arlettae; Spiked water and apple juice | Graphene electrode; bacteriophage | DL: 2 cfu Range: 2.0–2.0 × 106 cfu; Response time: 2 min Stability: 3 months |
[99] |
| E. coli; Cell cultures | SPCE; T4 phage | DL: 104 cfu mL−1, onset of lysis observed after 20 min | [110] |
| E. coli K12; milk | phage-functionalized screen-printed carbon microarrays; T4 phage-magnetic beads; | DL: 103 cfu mL−1 | [111] |
| blaNDM gene | SPCE; peptide nucleic acid, | DL: 200 nM | [57] |
| blaNDM gene | SPAuE; peptide nucleic acid | DL: 10 nM (synthetic targets), 100 pM (PCR products) | [112] |
| E. coli and methicillin-resistant S. aureus; cell culture | Interdigitated electrodes; antibody | Analysis time: <90 min; AST, 6 antibiotics tested; results compared with bacteria viability and conventional antibiogram assay | [113] |
| Amperometry | |||
| E. coli K-12, MG1655; cell culture | SPCE; activity of β-d-galactosidase in filtered cell lysate | DL: 1 cfu/100 mL for an incubation time of 8 h. | [114] |
| Differential Pulse Voltammetry | |||
| E. coli; Drinking water, apple juice, and skim milk | Thin film Pt electrode; engineered T7 phage; release of β-galactosidase | 105 cfu mL−1 for 3 h interaction; 102 cfu mL−1 after 7 h |
[115] |
| Square Wave Voltammetry | |||
| E. coli and Enterococcus spp.; pure cultures, water alfalfa sprouts, inoculated with E. coli and E. faecium | Screen-printed stencil electrodes on transparent film; release of β-galactosidase and β-glucuronidase (E. coli) and β-glucuronidase (Enterococcus) | DL: 10 cfu mL−1
E. coli after 4 h pre-culturing and 1 cfu mL−1 Enterococcus after 8 h culturing; DL: 2.3 × 102 cfu g−1 (E. coli) and 3.1 × 101 cfu g−1 E. faecium after 4 h and 12 h of pre-enrichment |
[116] |
| E. coli; cell cultures | SPCE modified with didodecyldimethylammonium bromide (DDAB); |
Test time: 2–5 h; resistance to cefepime, ampicillin, amikacin, and erythromycin | [117] |
| Chronocoulometry | |||
| E. coli JM105; cell culture | Screen-printed carbon electrode arrays modified with poly-l-lysine or chitosan; | IC50 chloramphenicol: 2.0 ± 0.2 mM; 17 antibiotics tested; 20 min test time; measurement of bacterial respiratory activity | [118] |
1 SPCE: screen-printed carbon electrodes; DL: detection limit; PNP: p-nitrophenol; SPAuE: screen-printed gold electrode.