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. 2020 Sep 1;25(17):3985. doi: 10.3390/molecules25173985

Table 2.

In vivo assessments of selected toxic substances.

Substance Radioisotope and Labeling Method Exposure Route Animal Model Results Ref.
Perfluorooctanoic acid 14C, incorporation Oral exposure Angus cows
  • Biodistribution of 14C-labeled perfluorooctanoic acid in blood, urine, and feces over 28 days and in tissues at the time of slaughter (28 days)

  • Measurement of plasma elimination half-life

[26]
Perfluorooctane sulfonate 35S, nucleophilic addition to [35S]SO2 Oral exposure C57BL/6 mice
  • Biodistribution of low and high doses of 35S-labeled perfluorooctane sulfonate in organs over 5 d

  • Whole-body autoradiogram of a mouse 48 h after oral administration

[28]
35S, nucleophilic addition to [35S]SO2 Gestational exposure Pregnant C57BL/6 mice
  • Biodistribution of 35S-labeled perfluorooctane sulfonate in the organs of dams, fetuses, and pups

  • Whole-body autoradiograms of pregnant mice 48 h and 96 h after exposure

[29]
Perfluorinated alkyl compounds 18F, isotopic exchange (19F → 18F) Intravenous injection CD1 mice
  • Biodistribution of 18F-labeled perfluorocarbons in organs over 4 h

  • Comparison of biological uptake values of three different perfluorocarbons (PFOA, PFHxA, PFBA)

[30]
Bisphenol A 14C, incorporation Intravenous and topical injection, percutaneous absorption SD rats (in vivo), human skin (in vitro)
  • Quantification of radioactivity in urine, feces, skin, and carcasses (14C-BPA mass balance) 1–72 h after administration

  • In vivo and ex vivo measurement of percutaneous 14C-BPA absorption

[35]
14C, incorporation Intraperitoneal injection Pregnant mice
  • Biodistribution of 14C-BPA in the organs of pregnant mice and newborn mice determined via autoradiography

[36]
14C, incorporation Percutaneous absorption Human skin (in vitro)
  • Kinetic measurements of 14C-BPA penetration

  • Distribution of 14C-BPA in the stratum corneum after incubation for 24 h

[37]
Manganese 52Mn Nasal inhalation, intravenous injection CD1 mice
  • Biodistribution of inhaled and injected 52Mn in organs over 24 h

  • Whole-body PET/CT imaging of intravenously injected 52Mn over 72 h

[38]
Graphene 125I, electrophilic substitution Intravenous injection BALB/c mice
  • Biodistribution of 125I-labeled graphene in organs over 60 days

  • Hepatic and renal toxicity over a three-month period after exposure

[39]
Graphene oxide 125I, electrophilic substitution Intratracheal instillation Kunming mice
  • Biodistribution of 125I-labeled graphene oxide in organs over 12 h

  • Whole-body SPECT/CT imaging for 1 h

  • Pulmonary toxicity over a three-month period after exposure

[40]
Graphene 14C, graphitization with 14C-labeled phenol Intake Daphnia magna
  • Quantification of 14C-labeled graphene uptake and excretion in different aqueous media

[41]
Graphene 14C, graphitization with 14C-labeled phenol Intratracheal instillation, oral exposure ICR mice
  • Biodistribution of 14C-labeled graphene in organs over 3 d (oral exposure) or 28 d (intratracheal instillation)

  • Quantification of translocation from the lungs to other internal organs

  • Pulmonary toxicity 24 h after exposure

[42]
Iridium NPs 192Ir, incorporation Nasal inhalation SD rats
  • Measurement of radioactive iridium NP (10, 15, 35, and 75 nm) retention half-life in the lungs

  • Quantification of translocation from the lungs to other internal organs

[43]
PHMG 111In, DOTA chelation Whole-body inhalation, intratracheal instillation SD rats
  • Biodistribution of 111In-labeled PHMG aerosols in organs over 168 h

  • Quantification of translocation from the lungs to other internal organs

  • Whole-body SPECT/CT imaging over 24 h

[44]
DEP 125I, self-assembly with 125I-labeled pyrene Intratracheal instillation, oral exposure ICR mice
  • Biodistribution of 125I-labeled DEP particles over 48 h

  • Whole-body SPECT/CT imaging over 48 h

[45]
LPS 111In, DOTA-BODIPY conjugate chelation Intravenous injection C57BL/6 mice
  • Biodistribution and SPECT/CT imaging of 111In-labeled LPS in organs over 24 h

  • Ex vivo fluorescence imaging of liver tissues

[46]
E. Coli 99mTc, [99mTc(CO)3] chelation with intracellular proteins Intravenous injection, oral exposure ICR mice
  • Organ biodistribution of 99mTc-labeled E. Coli over 8 h

  • Whole-body SPECT/CT imaging over 8 h

[47]
S. Aureus 99mTc, radiolabeled peptide attached to the cell membrane Intramuscular injection Swiss mice
  • Organ biodistribution of 99mTc-labeled S. Aureus over 28 h

  • Whole-body SPECT and fluorescence imaging of infected muscle over 28 h

[48]
AAV 124I, electrophilic substitution/modified Bolton–Hunter reagent Intraparenchymal injection CD-1 mice
  • Whole-body PET/CT imaging of 124I-labeled AAV over 8 h days

  • Measurement of brain uptake over 8 d

[49]
AAV 64Cu, NOTA chelation followed by conjugation on the AAV surface Intravenous injection C57BL/6 mice
  • Organ biodistribution of 64Cu-labeled AAV over 21 h

  • Whole-body PET/CT imaging over 21 h

  • Comparison of AAV9, AA9-TC, and PHP.eB viral capsid uptake by the brain

[50]