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. 2018 Jan 1;2(1):21–41. doi: 10.7150/ntno.22091

Table 1.

Summary of nanotechnologies for CTC detection.

Nanomaterial
/Device
Description Affinity ligand Efficiency % Purity % Viability % Cancer type
Metastatic (M)
Ref
Magnetic nanoparticles (MNPs) Ease of surface modification, controllable size, superparamagnetism and response to a magnetic field, high stability of surface chemistry, biocompatibility. EpCAM >94 -- 90.5 Colon/liver
/lung/breast
159
-- >75 -- -- -- 160
EpCAM/EGFR/HER2 90 -- -- -- 161
Gold nanoparticles (AuNPs) Simple synthesis, ease of surface modification, unique spectral properties, thiolated aptamers can be modified on AuNP surfaces through Au-S bonds. HER2 -- -- -- Breast 85
CD2/CD3 -- -- -- -- 87
Quantun dots (QDs) Inherent fluorescence, controllable size, long fluorescence lifetime, tunable emission wavelengths. EpCAM 86 -- 70 -- 81
EpCAM 70-80 18-23 -- -- 33
Graphene oxides (GO) High surface area-to-volume ratio, ease of surface modification, controllable size of its sheets, unique optical properties, biocompatibility. EpCAM 73 -- -- Breast/lung
/pancreatic
31
>40 -- 78 -- 92
Carbon nanotubes High surface area-to-volume ratio, good conductivity. EpCAM -- -- -- Liver 88
Nanoroughened surfaces The preference of cancer cells adhere to nanorough surfaces compared with normal blood cells. -- 80 14-84 -- -- 29
-- 90 -- -- -- 28
Si Nanopillars, (SiNP) Similar size to nanoscale components of the cell surface (e.g., filopodia and microvilli), allowing for increased local topographic interactions. EpCAM >40 -- 84-91 -- 66
EpCAM >70 -- 90 -- 107
Aptamer >80 >95 78-83 NSCCL 110
Nanofibers Ultralong nanofibers with controllable diameters that have similar dimensions with extracellular matrix (ECM) scaffolds and cell surface components. EpCAM 40-70 -- -- Colorectal
/gastric
67
CD146 87 -- -- Melanoma 120
Herringbone-
Chip (HBCTC-Chip/HB-chip)
A microfluidic mixing device with patterned herringbones on their upper surface to disrupt the laminar flow streamlines that cells travel. The chaotic microvortices increase the interactions between antibody-modified chip surfaces and target CTCs. EpCAM 91.8 14 95 M-prostate 95
-- -- -- M-pancreatic 139
-- -- -- Prostate 141
EpCAM/EGFR/HER2 80-90 -- -- Breast 150
75-95.9 78-90 85-90 Breast/Lung 122
80 53 90 M-lung 162
-- -- -- Breast/prostate 3
CSPG4/MCAM >90 0.3 -- M-melanoma 127
MagSweeper An immunomagnetic separation technology functionalized with a magnetic rod covered with a plastic sheath. Blood cells will be washed away by the movement of the magnetic rod and magnetic particles attached cells will be captured by a magnetic force produced by the magnetic rod. EpCAM >80 100 -- M-breast 163
>85 -- -- M-prostate 164
-- -- 50 Breast 71
MagSifter A magnetic sifter device functionalized with a section of a patterned pore array. Magnetically labeled target cells are captured at the pore edges and unlabeled cells pass through the pores. EpCAM >91.4 -- -- Lung 99
EpCAM -- -- -- Lung 14
Microchip-
based immunomagnetic
A microchip-based immunomagnetic separation that combines an immunomagnetic assay with a microfluidic device. EpCAM 86 -- -- -- 100
EpCAM 66 -- -- Breast/prostate
/lung
165
CTC-iChip A microchip-based immunomagnetic device performed by positioning cells in a near-single file line and targeted cell can be precisely deflected using a minimal magnetic force. EpCAM 96.7 >0.1 -- Prostate/breast
/pancreas
/colorectal/lung
102
Magnetic ranking cytometry (MagRC) A microchip-based immunomagnetic separation with X-shaped structures within the microfluidic channel that generates regions with slow flow and can be accurate for the in-line profiles of CTCs at the single-cell level. EpCAM 90 -- -- Prostate 104