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Table 1 Toxicokinetics of NMs

From: Nanomaterials and hepatic disease: toxicokinetics, disease types, intrinsic mechanisms, liver susceptibility, and influencing factors

Material

Size

Animal model

Administration

Biodistribution

Elimination

References

TiO2-NPs

21 nm

F344/DuCrlCrlj rats

10 mg/kg b.w., intravenous injection

Accumulated mostly in the liver (94% of the administration dose) and spleen (2.0%) at 6 h and did not decrease for up to 30 d

Extracted mostly into feces (15 ± 2.9 ng/h), followed by urine (0.27 ± 0.13 ng/h)

[200]

TiO2-NPs

70 nm

Wistar rats

40–400 μg/kg b.w., intravenous injection

Highest accumulations in the liver (95.5% of the injected dose) at 1 d, followed by the spleen

Extracted into the GIT then into feces (NM accumulations increase with time) and urine (decrease with time)

[19]

TiO2-NPs

8 nm

Wistar rats

40–240 μg/kg b.w., intratracheal instillation

Accumulated mostly in the lung; 1% passed through the ABB (4% of the IPLD) at 1 h

Cleared via the larynx into the GIT and translocated across the ABB into blood

[20]

Au-NPs

1.4–200 nm

Wistar rats

3.1–29 μg/rat, intravenous injection

Accumulated mostly in the liver (from 50 to 99%), followed by the spleen; exhibited a size- and surface charge-dependent distribution

Extracted into feces and urine

[28]

TiO2-NPs

40 nm

Wistar rats

30–80 μg/kg b.w., oral application

Accumulated mainly in the skeleton (0.98 ng/g), uterus (0.55 ng/g) and spleen (0.45 ng/g), and a few in the liver (0.09 ng/g) at 7 d

Mostly (0.6% of the applied dose) excreted in feces at 1 h, and 0.05% passed across the GIT barrier

[30]

Au-NPs

1.4–200 nm

Wistar rats

0.8–34.5 μg/rat, intratracheal instillation

Accumulated mostly in the lung (more than 94% at 24 h), and very few reached other organs

Cleared via the larynx and transported into the GIT and feces

[21]

TiO2-NPs

20 nm

Wistar rats

1.4 ± 0.5 μg/group, intratracheal instillation

Accumulated mostly in the lung, and 1% of the IPLD reached the liver and kidney

Cleared via the larynx into the GIT and translocation across the ABB, finally excreted in feces and urine

[26]

Ag-NPs

40 nm

Wistar rats

13.5 ± 3.6 μg, intratracheal instillation

Fractions of 0.14/ILD retained in the lung, 0.86 translocated across the ABB, 0.02 each retained in the liver and kidney, 0.48 and 0.22 found in the GIT and feces, respectively

Cleared via the larynx into the GIT or via the blood, liver, and gall bladder into the GIT, then excreted via feces

[168]