journal article·2015-01

Structural organization of C60 fullerene, doxorubicin, and their complex in physiological solution as promising antitumor agents

Yu. I. Prylutskyy, M. P. Evstigneev, V. V. Cherepanov, O. A. Kyzyma, L. A. Bulavin, N. A. Davidenko, P. Scharff

Journal of Nanoparticle Research· Volume 17· Issue 1
Publisher page

Abstract

Specific features of structural self-organization of C60 fullerene (1 nm size range), antitumor antibiotic doxorubicin (Dox) and their complex in physiological solution (0.9 % NaCl) have been investigated by means of atomic-force microscopy, dynamic light scattering, and small-angle X-ray scattering. Significant ordering of the mixed system, C60 + Dox, was observed, suggesting the complexation between these drugs, and giving insight into the mechanism of enhancement of Dox antitumor effect on simultaneous administration with C60 fullerene.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Fullerene Chemistry and Applications · Graphene research and applications · Boron and Carbon Nanomaterials Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (32)

Show source-provided references
1. Amer MS, Elliott JA, Maguire JF, Windle AH (2005) Calculations of the Raman spectra of C60 interacting with water molecules. Chem Phys Lett 411:395–39810.1016/j.cplett.2005.06.057 ↗
2. Andrievsky GV, Klochkov VK, Bordyuh AB, Dovbeshko GI (2002) Comparative analysis of two aqueous-colloidal solutions of C60 fullerene with help of FTIR reflectance and UV-Vis spectroscopy. Chem Phys Lett 364:8–1710.1016/S0009-2614(02)01305-2 ↗
3. Aschberger K, Johnston HJ, Stone V, Aitken RJ, Tran CL, Hankin SM et al (2010) Review of fullerene toxicity and exposure-appraisal of a human health risk assessment, based on open literature. Regul Toxicol Pharmacol 58:455–47310.1016/j.yrtph.2010.08.017 ↗
4. Avdeev MV, Khokhryakov AA, Tropin TV, Andrievsky GV, Klochkov VK, Derevyanchenko LI et al (2004) Structural features of molecular-colloidal solutions of C60 fullerenes in water by small-angle neutron scattering. Langmuir 20:4363–436810.1021/la0361969 ↗
5. Balch AL, Olmstead MM (1999) Structural chemistry of supramolecular assemblies that place flat molecular surfaces around the curved exteriors of fullerenes. Coord Chem Rev 185–186:601–61710.1016/S0010-8545(99)00013-2 ↗
6. Boyd PDW, Reed CA (2005) Fullerene-porphyrine constructs. Acc Chem Res 38:235–24210.1021/ar040168f ↗
7. Brant J, Lecoanet H, Wiesner MR (2005) Aggregation and deposition characteristics of fullerene nanoparticles in aqueous systems. J Nanopart Res 7:545–55310.1007/s11051-005-4884-8 ↗
8. Buchelnikov AS, Evstigneev MP (2014) Quantitative correlation of the in vitro biological effect with parameters of molecular complexation in mutagen-interceptor systems. J Theor Biol 357:268–27110.1016/j.jtbi.2014.06.016 ↗
9. Carvalho FS, Burgeiro A, Garcia R, Moreno AJ, Carvalho RA, Oliveira PJ (2014) Doxorubicin-induced cardiotoxicity: from bioenergetic failure and cell death to cardiomyopathy. Med Res Rev 34:106–13510.1002/med.21280 ↗
10. Cataldo F, Da Ros T (eds) (2008) Medicinal chemistry and pharmacological potential of fullerenes and carbon nanotubes. Carbon materials: chemistry and physics, vol 1. Springer, Dordrecht10.1007/978-1-4020-6845-4 ↗
11. Chen KL, Elimelech M (2009) Relating colloidal stability of fullerene (C60) nanoparticles to nanoparticle charge and electrokinetic properties. Environ Sci Technol 43:7270–727610.1021/es900185p ↗
12. Dallavalle M, Leonzio M, Calvaresi M, Zerbetto F (2014) Explaining fullerene dispersion by using micellar solutions. ChemPhysChem 15:2998–300510.1002/cphc.201402282 ↗
13. Deguchi S, Alargova RG, Tsujii K (2001) Stable dispersions of fullerenes, C60 and C70, in water. Preparation and characterization. Langmuir 17:6013–601710.1021/la010651o ↗
14. Evstigneev MP (2014) Hetero-association of aromatic molecules in aqueous solution. Int Rev Phys Chem 33:229–27310.1080/0144235X.2014.926151 ↗
15. Evstigneev MP, Buchelnikov AS, Voronin DP, Rubin YuV, Belous LF, Prylutskyy YuI et al (2013) Complexation of C60 fullerene with aromatic drugs. ChemPhysChem 14:568–57810.1002/cphc.201200938 ↗
16. Fortner JD, Lyon DY, Sayes CM, Boyd AM, Falkner JC, Hotze EM et al (2005) C60 in water: nanocrystal formation and microbial response. Environ Sci Technol 39:4307–431610.1021/es048099n ↗
17. Gharbi N, Pressac M, Hadchouel M, Szwarc H, Wilson SR, Moussa F (2005) [C60] fullerene is a powerful antioxidant in vivo with no acute or subacute toxicity. Nano Lett 5:2578–258510.1021/nl051866b ↗
18. Hirsch A, Brettreich M, Wudl F (2005) Fullerenes: chemistry and reactions. Wiley, New York
19. Labille J, Masion A, Ziarelly F, Rose J, Brant J, Villieras F et al (2009) Hydration and dispersion of C60 in aqueous systems: the nature of water-fullerene interactions. Langmuir 25:11232–1123510.1021/la9022807 ↗
20. Montellano A, Da Ros T, Bianco A, Prato M (2011) Fullerene C60 as multifunctional system for drug and gene delivery. Nanoscale 3:4035–404110.1039/c1nr10783f ↗
21. Panchuk RR, Prylutska SV, Chumak VV, Skorokhyd NR, Lehka LV, Evstigneev MP et al (2015) Application of C60 fullerene-doxorubicin complex for tumor cell treatment in vitro and in vivo. J Biomed Nanotechnol 11:1139–115210.1166/jbn.2015.2058 ↗
22. Piosik J, Zdunek M, Kapuscinski J (2002) The modulation by xanthines of the DNA-damaging effect of polycyclic aromatic agents, part II. The stacking complexes of caffeine with doxorubicin and mitoxantrone. Biochem Pharmacol 63:635–64610.1016/S0006-2952(01)00903-0 ↗
23. Prylutska SV, Grynyuk II, Matyshevska OP, Prylutskyy YuI, Ritter U, Scharff P (2008) Anti-oxidant properties of C60 fullerenes in vitro. Fuller Nanotub Carbon Nanostruct 16:698–70510.1080/15363830802317148 ↗
24. Prylutska SV, Burlaka AP, Klymenko PP, Grynyuk II, Prylutskyy YuI, Schuetze Ch et al (2011) Using water-soluble C60 fullerenes in anticancer therapy. Cancer Nanotechnol 2:105–11010.1007/s12645-011-0020-x ↗
25. Prylutska S, Bilyy R, Overchuk M, Bychko A, Andreichenko K, Stoika R et al (2012) Water-soluble pristine fullerenes C60 increase the specific conductivity and capacity of lipid model membrane and form the channels in cellular plasma membrane. J Biomed Nanotechnol 8:522–52710.1166/jbn.2012.1404 ↗
26. Prylutska S, Grynyuk I, Matyshevska O, Prylutskyy Y, Evstigneev M, Scharff P, Ritter U (2014) C60 fullerene as synergistic agent in tumor-inhibitory doxorubicin treatment. Drugs R D 14:333–34010.1007/s40268-014-0074-4 ↗
27. Prylutskyy YuI, Buchelnikov AS, Voronin DP, Kostjukov VV, Ritter U, Parkinson JA et al (2013) C60 fullerene aggregation in aqueous solution. Phys Chem Chem Phys 15:9351–936010.1039/c3cp50187f ↗
28. Prylutskyy YuI, Petrenko VI, Ivankov OI, Kyzyma OA, Bulavin LA, Litsis OO et al (2014a) On the origin of C60 fullerene solubility in aqueous solution. Langmuir 30:3967–397010.1021/la404976k ↗
29. Prylutskyy YuI, Evstigneev MP, Pashkova IS, Wyrzykowski D, Woziwodzka A, Gołuński G et al (2014b) Characterization of C60 fullerene complexation with antibiotic doxorubicin. Phys Chem Chem Phys 16:23164–2317210.1039/C4CP03367A ↗
30. Skamrova GB, Laponogov I, Buchelnikov AS, Shckorbatov YG, Prylutska SV, Ritter U et al (2014) Interceptor effect of C60 fullerene on the in vitro action of aromatic drug molecules. Eur Biophys J 43:265–27610.1007/s00249-014-0960-2 ↗
31. Traganos F, Kapuscinski J, Darzynkiewicz Z (1991) Caffeine modulates the effects of DNA-intercalating drugs in vitro: a flow cytometric and spectrophotometric analysis of caffeine interaction with novantrone, doxorubicin, ellipticine, and the doxorubicin analogue AD198. Cancer Res 51:3682–3689
32. Woziwodzka A, Gołuński G, Wyrzykowski D, Kaźmierkiewicz R, Piosik J (2013) Caffeine and other methylxanthines as interceptors of food-borne aromatic mutagens: inhibition of Trp-P-1 and Trp-P-2 mutagenic activity. Chem Res Toxicol 26:1660–167310.1021/tx4002513 ↗