3D printed microfluidic biosensor |
Aptamer coated magnetic beads with magnetic separation |
Plasmodium falciparum lactate dehydrogenase (PfLDH) enzyme |
Colorimetric |
Parasitemia < 0.01% |
180 min |
[109] |
Enzyme-linked LTF assay (ELLTA) |
Long tail fibers (S16 LTF) of bacteriophages immobilized onto paramagnetic beads |
Salmonella typhimurium
|
Colorimetric |
102 cfu/mL |
2 h |
[110] |
Assay |
Magnetic beads coated with the engineered chimeric human opsonin protein, Fc-mannose-binding lectin (FcMBL) |
Articular fluid samples and synovial tissue samples from patients with S. aureus infections |
RT-PCR analysis and MALDI-TOF |
76% ± 5.7% capture efficiency |
- |
[111] |
Assay |
Iron oxide magnetic nanoparticles functionalized with bacterial species-identifiable aptamers |
S. aureus and E. coli
|
Fluorescence microscopy |
10 CFU |
1.5 h |
[112] |
Microfluidic platform |
Induced advectivespiral flows of super-paramagnetic nanoparticles coated with mannose-binding lectin and magnetic separation |
E. coli spiked into undiluted rat whole blood |
None |
91.68% ± 2.18% capture efficiency |
- |
[113] |
3D Nano-biointerface platform |
Zinc oxide nanorod array 3D nano–bio surface functionalized with lectin Concanavalin A |
E. coli
|
Fluorescence microscopy imaging |
0.9 × 102 CFU/mL |
- |
[114] |
Nanowire arrays |
Functionalized 3D nanowire substrate |
S. aureus
|
Fluorescence microscopy |
10 CFU/mL |
30 min |
[115] |
Nanowire arrays |
Bendable polycrystalline nanowires pre-grafted on 3D carbon foam |
Human blood spiked with Salmonella spp
|
Fluorescence microscopy |
~97% capture efficiency |
- |
[116] |
Impedanceelectrode sensor |
Antibacterial prickly Zn-CuO nanoparticles with burr-like nanostructures |
Rat blood spiked with E. coli
|
Impedance-based electrode sensor |
10 CFU/mL |
20 min |
[117] |
Surface-Enhanced Raman Scattering Multi-Multifunction Chip |
4-mercaptophenylboronic acid |
Humanblood spiked with E.coli, S. aureus
|
Surface-Enhanced Raman Scattering |
1.0 × 102 cells m/L |
- |
[118] |
Photoelectrochemical platform |
4-mercaptophenylboronic acid |
E. coli
|
Photoelectrode |
46 CFU/mL |
30 min |
[119] |
Microfluidic platform |
Magainin 1 peptide |
urine spiked with Salmonella spp; Brucella spp
|
Recombinase polymerase amplification (RPA) sensor |
5 CFU/mL urine for Salmonella; 10 CFU/mL for Brucella
|
60 min |
[120] |
Microfluidic chip |
Bulk acoustophoresis |
diluted whole blood spiked with Pseudomonas putida
|
Microscopy |
- |
12.5 min |
[121] |
Microfluidic chip |
Bulk acoustophoresis |
Pseudomonas aeruginosa, S. aureus, E. coli
|
Luminescent bacterio-phage assay |
45% to 60% capture efficiency |
- |
[122] |
Microfluidic capillaric circuit |
Antibody-functionalized microbeads |
synthetic urine spiked with E. coli
|
Fluorescence microscopy |
1.2 × 102 CFU/mL |
7 min |
[123] |
Microfluidic chip |
Pillar-assisted self-assembly microparticles Nano- filter for |
E. coli from samples |
Fluorescence microscopy |
capture efficiency of 93% |
- |
[124] |
Reusable supramolecular platform |
Multilayered film and β-cyclodextrin (β-CD) derivatives modified with mannose |
Type I fimbriae E. coli and lectin proteins |
Fluorescence microscopy |
Capture efficiency of 93% |
- |
[125] |
Photonic PCR on a chip |
Gravity-driven cell enrichment |
E. coli
|
Photonic PCR on a chip |
103 CFU/mL |
10 min |
[126] |
Enzyme-linked lectin sorbent assay (ELLecSA) |
Fc-mannose-binding lectin |
Bacteria, fungi, virus, parasites. LPS, LTA from Gram-negative and Gram-positive bacteria, as well as lipo-arabino-mannan (LAM) and phosphatidyl-inositol mannoside from M. tuberculosis
|
Scanning electron microscopy |
- |
<1 h |
[114] |
Fluorometric assay |
Two distinct terminal phosphate-labeled LPS specific aptamers attached onto Zr-MOFs to fabricate the magnetic core-shell for magnetic separation |
Acinetobacter baumannii in blood samples |
Fluorescent signal amplification by fluorescence probes |
10 cfu/mL |
~2.5 h |
[127] |