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. 2021 Apr 16;11(1):8362.
doi: 10.1038/s41598-021-87014-3.

Evaluation of the C60 biodistribution in mice in a micellar ExtraOx form and in an oil solution

Affiliations

Evaluation of the C60 biodistribution in mice in a micellar ExtraOx form and in an oil solution

Konstantin N Semenov et al. Sci Rep. .

Abstract

The article is devoted to the study of the pharmacokinetics of fullerene C60 in oil and micellar forms, analysis of its content in blood, liver, lungs, kidneys, heart, brain, adrenal glands, thymus, testicles, and spleen. The highest accumulation of C60 was found in the liver and adrenal glands. As a result of the studies carried out, it was shown that the bioavailability of C60 in the micellar form is higher than that in an oil solution.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
13C NMR spectrum of C60 obtained with CP/MAS technique.
Figure 2
Figure 2
MALDI mass spectrum of C60 fullerene.
Figure 3
Figure 3
IR spectrum of C60 fullerene.
Figure 4
Figure 4
A chemical structure of TWEEN-80.
Figure 5
Figure 5
Size distribution of a C60 micellar form.
Figure 6
Figure 6
Absorption spectrum of fullerene C60 in olive oil.
Figure 7
Figure 7
Triglyceride molecule consisting of two oleic acid residues and one palmitic acid residue.
Figure 8
Figure 8
Cell with fullerene molecule and 20 triglyceride molecules.
Figure 9
Figure 9
HPLC–MS chromatogram of C60.
Figure 10
Figure 10
Solubility polytherm of fullerene C60 in olive oil in the temperature range 0–80 °C.
Figure 11
Figure 11
A density field of oleic residues in a system under study.
Figure 12
Figure 12
Pharmacokinetics of fullerene C60 in whole blood after oral administration to mice of an oil solution (–■–) and micellar form of fullerene C60 (–●–). Dots are experimental points; lines represent Eq. 2.

References

    1. Friedman SH, et al. Inhibition of the HIV-1 protease by fullerene derivatives: model building studies and experimental verification. J. Am. Chem. Soc. 1993;115:6506–6509. doi: 10.1021/ja00068a005. - DOI
    1. Friedman SH, Ganapathi PS, Rubin Y, Kenyon GL. Optimizing the binding of fullerene inhibitors of the HIV-1 protease through predicted increases in hydrophobic desolvation. J. Med. Chem. 1998;41:2424–2429. doi: 10.1021/jm970689r. - DOI - PubMed
    1. Jafvert CT, Kulkarni PP. Buckminsterfullerene’s (C60) octanol-water partition coefficient (Kow) and aqueous solubility. Environ. Sci. Technol. 2008;42:5945–5950. doi: 10.1021/es702809a. - DOI - PubMed
    1. Lin Y-L, et al. Light-independent inactivation of Dengue-2 virus by carboxyfullerene C3 isomer. Virology. 2000;275:258–262. doi: 10.1006/viro.2000.0490. - DOI - PubMed
    1. Piotrovsky LB, Kiselev OI. Fullerenes and viruses. Fullerenes Nanotub. Carbon Nanostruct. 2005;12:397–403. doi: 10.1081/FST-120027198. - DOI

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