TABLE 2.
Summary of Quantum Dot Toxicity Studies Published Prior to September 2005.
QD composition | Cell, tissue, or organism tested | [QD] used | Exposure time | Observed toxicity | Reference |
CdTe | PC12 (rat pheochronocytoma) and N9 (murine microglia) cell lines | 0.01–100 μg/ml | 2–24 h | Cytotoxic: 10 μg/ml | (Lovric et al., 2005) |
CdSe/ZnS-DHLA QDs | B16F10 cells injected into mice | Injected 20,000–40,000 QD-treated cells into mice. | 4–6 h cell incubation time, mice sacrificed at 1–6 h | Not toxic: No toxicity observed in cells or mice. | (Voura et al., 2004) |
CdSe/ZnS-MUA | Vero and HeLa cell lines; primary human hepatocytes | 0–0.4 mg/ml | 24 h | Cytotoxic: 0.2 mg/ml in Vero cells, 0.1 mg/ml in HeLa cells, 0.1 mg/ml in hepatocytes. | (Shiohara et al., 2004) |
CdSe/ZnS-SSA | EL-4 cells (mouse lymphocytes) | 0.1–0.4 mg/ml | 0–24 h | Cytotoxic: 0.1 mg/ml altered cell growth; most cells nonviable at 0.4 mg/ml. | (Hoshino et al., 2004b) |
CdSe/ZnS-SSA | EL-4 cells labelled with QDs and injected into mice | 0.1 mg/ml QDs per 5 × 107 cells | 2 h to 7 days | Not toxic: No toxicity observed in mice in vivo. | (Hoshino et al., 2004b) |
CdSe/ZnS conjugates: NH2, OH, OH/COOH, H2/OH, MUA, COOH | WTK1 cells | 1–2μM | 12 h | Cytotoxic: 2μM QD-COOH induced DNA damage at 2 h. | (Hoshino et al., 2004a) |
CdSe-MAA, TOPO QDs | Primary rat hepatocytes | 62.5–1000 μg/ml | 1–8 h | Cytotoxic: A concentration of 62.5 μg/ml was cytotoxic under oxidative/photolytic conditions. No toxicity observed on addition of ZnS cap to QDs. | (Derfus et al., 2004) |
CdSe/ZnS | HeLa cells | 10 pmol QDs per 10,000 cells (approx. 10nM) | 10 days (cell culture) | Not cytotoxic: 10nM QD had minimal impact on cell survival. | (Chen and Gerion, 2004) |
CdSe/ZnS amp-QDs, and mPEG QDs | Mice—QDs injected into tail vein | Injections of approx. 180nM, or 20 pmol/g animal weight | 15-min cell incubations, 1–133 days in vivo | Not toxic: No signs of localized necrosis at the sites of deposition. | (Ballou et al., 2004) |
CdSe/ZnS-amphiphilic micelle | Mice—QDs injected into tail vein | 60μM/gram animal weight, 1μM and 20nM final [QD]. | Not indicated. | Mice showed no noticeable ill effects upon imaging. | (Larson et al., 2003) |
CdSe/ZnS-DHLA | Dictyostelium discoideum and HeLa cells | 400–600nM | 45–60 min | No effects on cell growth noted. | (Jaiswal et al., 2003) |
Avidin-conjugated CdSe/ZnS QDs | HeLa cells | 0.5–1.0μM | 15 min | No effect on cell growth or development noted. | (Jaiswal et al., 2003) |
CdSe/ZnS-MUA QDs; QD-SSA complexes | Vero cells | 0.24 mg/ml | 2 h | Not cytotoxic: 0.4 mg/ml MUA/SSA-QD complexes did not affect the viability of Vero cells. | (Hanaki et al., 2003) |
QD micelles: CdSe/ZnS QDs in (PEG-PE)and phosphati-dylcholine | Xenopus blastomeres | 5 × 109 QDs/cell (approx. 0.23 pmol/cell) | Days | Toxic: At a threshold of 5 × 109 QDs/cell, observed cell abnormalities, altered viability and motility. | (Dubertret et al., 2002) |
Note. PEG, polyethylene glycol.