Table 1.
Nanotubes | Surfactant | Biological System | Dose | Exposure Time | Assay Method | Conclusion | Reference |
---|---|---|---|---|---|---|---|
HiPco SWCNTs | PLPEG | Human serum and intravenous injection in rats | 60 μg/mL | 0.5 h | ELISA | Activation of the complement system by SWCNTs in undiluted normal human serum and in vivo rats. | [18] |
HiPco SWCNTs | PLPEG | Intravenous/brain injection in rats | 60 μg/mL | 0.5 h to days | Fluorescence | In vivo SWCNT circulation (vascular system, brain). Stable imaging in vivo and in tissues. | [11,17] |
HiPco SWCNTs | Pluronic F108 | J774.1A mouse peritoneal macrophage | 11 ng/mL | 0, 8, 18 and 24 h | Fluorescence | Macrophages can ingest significant quantities of SWCNTs without showing toxic effects. Stable imaging in cells. | [19] |
HiPco SWCNTs | Pluoronic F127 | HeLa cells | 200 μg/mL | 2 days | Fluorescence imaging | Induction of actin bundling in cells, reduced cellular proliferation. | [20] |
Arc Discharge SWCNTs | Tween20 | Pathgen free guinea pigs | 50 mg/mL | 4 weeks | Lung function, bronchoalveolart lavega | No abnormalities of pulmonary function or measurable inflammation in guinea pigs. | [21] |
MWCNTs | Sterile saline + Brij 35 | Incubation with cytochrome P450 enzymes (CYP3A4) | 0.067 mg/mL | 5 min at 37 °C | Capillary electrochromatography, enzyme activity monitoring | No effect on CYP3A4 activity. Substantial improvement of migration time and peak shape repeatability in capillary electrochromatography. | [22] |
HiPco SWCNTs | ISPVP | Human embryonic kidney cells (HEK cells) | 1/30 μg/mL | 5 min at RT or 12 h at 37 °C | Fluorescence | Stable imaging in cells. | [23] |
HiPco: High-Pressure carbon monoxide; SWCNTs: Single-walled Carbon Nanotubes; MWCNTs: Multi-walled Carbon Nanotubes; PLPEG: Phospholipid-polyethylene Glycol; ISPVP: In Situ Polymerized (poly)vinyl pyrrolidone.