4.7 Article

In Vitro Studies Demonstrate Antitumor Activity of Vanadium Ions from a CaO-P2O5-CaF2:V2O5 Glass System in Human Cancer Cell Lines A375, A2780, and Caco-2

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Publisher

MDPI
DOI: 10.3390/ijms24021149

Keywords

phosphate glasses; V2O5 ions; pH measurements; Fourier transform infrared (FT-IR); antitumor activity; MTT assay

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In this research, the structural and biological properties of V2O5-doped phosphate glasses were investigated. A xV(2)O(5)center dot(100 - x)[CaF2 center dot 3P(2)O(5)center dot CaO] glass system was synthesized and analyzed using various techniques. In vitro tests were conducted to evaluate the antitumor activity of the V2O5-doped glass compared to the matrix and control. The results indicate that the V2O5-doped glass has a high dissolution rate and cytotoxic potential as an antitumor agent.
In this research, we investigated the structural and biological properties of phosphate glasses (PGs) after the addition of V2O5. A xV(2)O(5)center dot(100 - x)[CaF2 center dot 3P(2)O(5)center dot CaO] glass system with 0 <= x <= 16 mol% was synthesized via a conventional melt-quenching technique. Several analysis techniques (dissolution tests, pH, SEM-EDS, FT-IR, and EPR) were used to obtain new experimental data regarding the structural behavior of the system. In vitro tests were conducted to assess the antitumor character of V2O5-doped glass (x = 16 mol%) compared to the matrix (x = 0 mol%) and control (CTRL-) using several tumoral cell lines (A375, A2780, and Caco-2). The characterization of PGs showed an overall dissolution rate of over 90% for all vitreous samples (M and V1-V7) and the high reactivity of this system. EPR revealed a well-resolved hyperfine structure (hfs) typical of vanadyl ions in a C-4v symmetry. FT-IR spectra showed the presence of all structural units expected for P2O5, as well as very clear depolymerization of the vitreous network induced by V2O5. The MTT assay indicated that the viability of tumor cells treated with V7-glass extract was reduced to 50% when the highest concentration was used (10 mu g/mL) compared to the matrix treatment (which showed no cytotoxic effect at any concentration). Moreover, the matrix treatment (without V2O5) provided an optimal environment for tumor cell attachment and proliferation. In conclusion, the two types of treatment investigated herein were proven to be very different from a statistical point of view (p < 0.01), and the in vitro studies clearly underline the cytotoxic potential of vanadium ions from phosphate glass (V7) as an antitumor agent.

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