Table 2.
Methods | Exosome sources | Sample volume | Sensing mechanism | Sensing substances | Detection limit | Ref. |
---|---|---|---|---|---|---|
Colorimetric Detection | MCF-7 cells and breast cancer patient’s serum | H2O2-mediated oxidation of TMB | s-SWCNTs; CD63-specific aptamer | 5.2 × 105 particles/μL | [109] | |
Cell-culture medium and prostate cancer patient’s plasma | 500 μL | H2O2-mediated oxidation of TMB | Aptamer-capped Fe3O4 nanoparticles | 3.58 × 106 particles/mL | [72] | |
Urine | 100 mL | H2O2-mediated oxidation of TMB | Biotinylated anti-CD63 antibody; streptavidin-labeled HRP | 35.0 AU/mL | [76] | |
MCF-7 cells and cancer patient’s serum | 100 μL | H2O2-mediated oxidation of TMB | CD9, CD63 antibody mixture; HRP-labeled secondary antibody | 2.2 × 104 particles/μL | [110] | |
BeWo cell | H2O2-mediated oxidation of TMB | Au-NP; Fe2O3NC | 103 exosomes/mL | [148] | ||
Fluorescence Detection | Plasma specimens from NSCLC and OVCA patients | 30 μL | Chemifluorescence reagents | EpCAM, IGF-1R or CA125 antibodies; AP-conjugated secondary antibody, and the DiFMUP substrate | 0.281 pg/mL; 0.383 pg/mL | [36] |
SKOV3 cells and plasma of OVCA patients | 10 μL | The reaction of SβG with FDG | Biotin conjugated detection antibodies and streptavidin conjugated SβG | 21 exosomes/μL | [149] | |
MCF-7 and MDA-MB-231 cell culture medium | 1 mL | Fluorescent carbocyanine dye (DiO) | CD63 antibody functionalized microbead and DIO labelling | [150] | ||
Cell culture supernatant and serum from pancreatic cancer patients | Fluorescent carbocyanine dye (DiO) | CD63 antibody-functionalized EXOchip | [20] | |||
MCF-7 cells and blood samples from cancer patients | 100-300 μL | Fluorescent second antibody | Anti-EpCAM antibody and Alexafluor®647-conjugated secondary antibody | [59] | ||
Cell-culture medium and plasma from breast cancer patients | Fluorescent second antibody | CD63 antibody-coated magnetic beads; fluorescent dye-conjugated antibodies | 107 particles/μL | [151] | ||
A549 cancer cell line and plasma samples of lung cancer patients | 0.5 μL | Fluorescent aptamer | TMR-aptamer | 500 particles/μL | [152] | |
Serum samples | Fluorescent aptamer | CD63 aptamer-modified magnetic beads; Cy3-labeled short sequence | 1.0 × 105 particles/μL | [126] | ||
Cancer cell line and plasma samples | 500 μL | Fluorescent aptamer | TPE-TAs/aptamer complexes; graphene oxide surface | 3.43 × 105 particles/μL | [99] | |
MDA-MB-231 cell-culture medium and plasma from breast cancer patients | 80 μL | Fluorescence quenching | GPC-1 antibody coated magnetic beads; CD63 aptamer | 6.56 × 104 particles/μL | [84] | |
Cancer cell line and serum samples | Fluorescence quenching | FAM-labeled aptamers; graphene oxide | 1.6 × 105 particles/mL | [113] | ||
Cancer cell line and blood samples | Fluorescence quenching | Anti-CD63-PE/MoS2–MWCNT | 14.8 × 105 particles/mL | [153] | ||
Electrochemical Detection | Ovarian cancer cell lines and plasma from patients with ovarian cancer | 10 μL | Integrated magneto-electrochemical sensor | Immunomagnetic beads; HRP-labeled secondary antibody | 3 × 104 | [128] |
Plasma samples | 20 μL | Electrochemical biosensor | Immunomagnetic beads; probing antibodies | [129] | ||
Cell-culture medium and blood samples from breast cancer patients | Electrochemical biosensor | Anti-PD-L1-linked DNA strand; PVP@HRP@ZIF-8 | 334 particles/mL | [114] | ||
HepG2 cells and human serum of liver cancer patients | 30 μL | Aptamer-based biosensors | CD63 aptamer and mimicking DNAzyme sequence | 4.39 × 103 particles/mL | [65] | |
Culture medium of HepG2 cells | Aptamer-based biosensors | NTH-assisted aptasensor | 2.09 × 104/mL | [154] | ||
Cell-culture medium and serum | Aptamer-based biosensors | Aptamer-magnetic bead bioconjugates; electroactive Ru (NH3)63+ | 70 particles/μL | [155] | ||
Cellular supernatant and human plasma samples | Aptamer-based biosensors | anti-CD63 antibody modified gold electrode and a gastric cancer exosome specific aptamer | 9.54 × 102/mL | [156] | ||
Human hepatoma cell lines MHCC97H/L and mouse melanoma cell lines B16-F1/10 | Antibody microarray SPRi sensor | Anti-CD9, CD41b,21 and tyrosine kinase receptor MET8a antibodies immobilized gold-coated glass sensor chip | [157] | |||
SPR Detection | MCF-7 breast cancer cells and MCF-10A normal breast cells | SPR-based aptasensor | Dual gold nanoparticle-assisted signal amplification | 5 × 103 exosomes/mL | [158] | |
Human NSCLC cell lines, normal lung cell and plasma | 1.5 mL | Bioaffinity interactions of antibodies and different recognition sites | Antibodies modified-gold chip and different recognition sites | 104 particles/μL | [159] | |
Urine samples from lung cancer patients and controls | 500 μL | SPR-induced improved scattering intensity | Anti CD81/LRG1 antibody modified nanoporous gold nanocluster membrane; second antibody-conjugated Au nanorod probes | < 1000 particles/mL | [58] | |
Breast cancer cell line and serum | 250 μL | SPR-induced improved scattering intensity | Anti-HER2-functionalised SPR chip | 8280 exosomes/μL | [160] | |
Cancer cells and serum and the CSF of an orthotopic mouse model | Strong localization of surface plasmon polaritons | TIC-AFM and TiN–NH-LSPR biosensors | 5.29 × 10−1 μg/ml; 3.46 × 10 -3 μg /ml | [161] | ||
Breast cancer cells and normal breast cells; plasma from HER2-positive breast cancer patients | Raman reporters | Gold-coated glass microscopy slide; QSY21-coated gold nanorods | 2 × 106/mL | [134] | ||
SERS | Plasma of cancer patients | 400 μL | P-O bond signature | Beehives-like Au-coated TiO2 macroporous inverse opal | [117] | |
Cell-culture medium and serum sample | 4 μL | MBA signature | Fe3O4@TiO2 nanoparticles; anti-PD-L1 antibody modified Au@Ag@MBA | 1 PD-L1 exosome/μL | [90] | |
Normal and lung cancer cell lines; plasma | Deep learning | Deep learning model | [162] | |||
Cell-culture medium; serum and plasma | < 1 μL | Enrichment of aptamer-bound EVs | Seven aptamers targeting specific proteins; machine-learning algorithm | 3.3 × 103/μl | [68] | |
CRISPR/Cas-assisted detection | A549 cell-culture medium and serum from lung cancer patients | CRISPR/Cas12a | CD63 aptamer; CRISPR/Cas12a | Linear range of 3 × 103–6 × 107 particles/μL | [136] | |
SUNE2 cell-culture medium and serum from NPC patients | 50 μL | CRISPR/Cas12a | Nucleolin and PD-L1 aptamers; CRISPR/Cas12a | 102 particles/μL | [137] | |
SUNE2 cell-culture medium and serum from NPC patients | CRISPR/Cas12a | CD109 and EGFR aptamers; CRISPR/Cas12a | 102 particles/μL | [138] | ||
Single EV Analysis | Human serum | 10 μL | Rolling circle amplification | ssDNA-assisted single EV detection platform | 82 vesicles/μL | [139] |
T3M4 pancreas cancer line and serum from PDAC patients | 10 mL | Flow cytometry | Aldehyde/sulfate latex beads; anti-GPC-1 antibody and Alexa-488-tagged antibody | [38] | ||
Breast cancer cell lines and serum of breast cancer patients | 500 μL | Flow cytometry | Aldehyde/sulfate latex beads; anti-EpCAM or anti-HER2 antibody; Alexa-488- or − 594-tagged secondary antibodies | [141] | ||
Human cell lines and serum of glioma patients | 250 μL | Flow cytometry | Aldehyde/sulfate latex beads; anti-EGFR or anti-CXCR4 antibody | [118] | ||
HCT15 cell-culture medium and plasma | 500 μL | Nano-flow cytometry | [142] |
OVCA Ovarian cancer, PGR Progesterone receptor, ESR1 Estrogen receptor 1, ERBB2 erb-b2 receptor tyrosine kinase 2