Ukr.Biochem.J. 2025; Volume 97, Issue 6, Nov-Dec, pp. 134-141
doi: https://doi.org/10.15407/ubj97.06.134
Benzofuran thiazole derivative complexation with polymeric nanoparticles enhances reduction of mitochondrial membrane potential in murine lymphoma cells
Ya. R. Shalai1*, A. V. Salamovska1, M. V. Ilkiv1, B. O. Manko1,
Yu. V. Ostapiuk2, N. E. Mitina3, O. S. Zaichenko3, A. M. Babsky1
1Biology Faculty, Ivan Franko National University of Lviv, Ukraine;
2Chemistry Faculty, Ivan Franko National University of Lviv, Ukraine;
3Department of Organic Chemistry, Lviv Polytechnic National University, Ukraine;
*e-mail: Yaryna.Shalay@lnu.edu.ua
Received: 01 August 2025; Revised: 17 September 2025;
Accepted: 28 November 2025; Available on-line: 23 December 2025
The development of new anticancer drugs aimed at the inhibition of mitochondria functioning in tumor cells is a promising approach to cancer treatment. The aim of our study was to investigate the effect of benzofuran derivative N-(5-benzyl-1,3-thiazol-2-yl)-3,5-dimethyl-1-benzofuran-2-carboxamide (BF1) and its complex with polymer nanoparticles based on polyethylene glycol (PEG-PN) on mitochondrial membrane potential in cells of NK/Ly lymphoma grafted in ascite form in mice. Relative values of mitochondrial potential at different exposure times were recorded using the fluorescent dye tetramethylrhodamine. Fluorescence microscopy showed a significant decrease in mitochondrial potential after 30 and 60 min of cells incubation with the BF1-PEG-PN complex but not with unconjugated BF1. After 120 min of incubation, a decrease in the studied parameter was observed under the action of both BF1 alone and its complex with PEG-PN. The data obtained showed that a possible mechanism of cytotoxic action of the BF1 complex with PEG-PN involves early mitochondria depolarization in lymphoma cells.
Keywords: benzofuran derivative, complexation, mitochondrial membrane potential, NK/Ly lymphoma cell, polymeric nanoparticle
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