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C60 Fullerene as an Effective Nanoplatform of Alkaloid Berberine Delivery into Leukemic Cells

Authors :
Anna Grebinyk
Svitlana Prylutska
Anatoliy Buchelnikov
Nina Tverdokhleb
Sergii Grebinyk
Maxim Evstigneev
Olga Matyshevska
Vsevolod Cherepanov
Yuriy Prylutskyy
Valeriy Yashchuk
Anton Naumovets
Uwe Ritter
Thomas Dandekar
Marcus Frohme
Source :
Pharmaceutics, Vol 11, Iss 11, p 586 (2019)
Publication Year :
2019
Publisher :
MDPI AG, 2019.

Abstract

A herbal alkaloid Berberine (Ber), used for centuries in Ayurvedic, Chinese, Middle-Eastern, and native American folk medicines, is nowadays proved to function as a safe anticancer agent. Yet, its poor water solubility, stability, and bioavailability hinder clinical application. In this study, we have explored a nanosized carbon nanoparticle—C60 fullerene (C60)—for optimized Ber delivery into leukemic cells. Water dispersions of noncovalent C60-Ber nanocomplexes in the 1:2, 1:1, and 2:1 molar ratios were prepared. UV−Vis spectroscopy, dynamic light scattering (DLS), and atomic force microscopy (AFM) evidenced a complexation of the Ber cation with the negatively charged C60 molecule. The computer simulation showed that π-stacking dominates in Ber and C60 binding in an aqueous solution. Complexation with C60 was found to promote Ber intracellular uptake. By increasing C60 concentration, the C60-Ber nanocomplexes exhibited higher antiproliferative potential towards CCRF-CEM cells, in accordance with the following order: free Ber < 1:2 < 1:1 < 2:1 (the most toxic). The activation of caspase 3/7 and accumulation in the sub-G1 phase of CCRF-CEM cells treated with C60-Ber nanocomplexes evidenced apoptosis induction. Thus, this study indicates that the fast and easy noncovalent complexation of alkaloid Ber with C60 improved its in vitro efficiency against cancer cells.

Details

Language :
English
ISSN :
19994923
Volume :
11
Issue :
11
Database :
Directory of Open Access Journals
Journal :
Pharmaceutics
Publication Type :
Academic Journal
Accession number :
edsdoj.f2cdd4eff1e1406f9846cb1084b92860
Document Type :
article
Full Text :
https://doi.org/10.3390/pharmaceutics11110586