The in vitro anticancer activity of the dinuclear trithiolato-bridged arene ruthenium complex diruthenium-1 (DiRu-1) was evaluated against a panel of human cancer cell lines used as in vitro models for hepatocellular carcinoma (HepG2 cells), estrogen-responsive breast adenocarcinoma (MCF-7 cells), and triple-negative breast adenocarcinoma (MDA-MB-231 cells). DiRu-1 is highly cytotoxic to these cell lines, demonstrating half-maximal inhibitory concentrations (IC ) in the low-nanomolar range (77±1.4 to 268.2±4.4 nm). The main molecular mechanisms responsible for the high cytotoxicity of DiRu-1 against the most responsive MCF-7 cell line (IC =77±1.4 nm) were investigated on the basis of the capacity of DiRu-1 to induce oxidative stress, apoptosis, and DNA damage, and to inhibit the cell cycle and proliferation. The results show that DiRu-1 triggers caspase-dependent apoptosis in MCF-7 cells on both the intrinsic and extrinsic pathways. Moreover, the Ru complex also causes necrosis, mitotic catastrophe, and autophagy. DiRu-1 increases the intracellular levels of reactive oxygen species (ROS), which play a significant role in its cytotoxicity and pro-apoptotic activity. An important mechanism of the anticancer activity of DiRu-1 appears to be the induction of DNA lesions, mainly due to apoptotic DNA fragmentation and cell-cycle arrest at the G /M checkpoint. These changes are correlated with the concentration of DiRu-1, the duration of the cell treatment, and the post-treatment time.
Spinel Mn(x)Zn(1-x)Fe2O4 (0.0 ≤ x ≤ 1.0) nanoparticles (NPs) were successfully synthesized by a facile one-pot microwave combustion method using urea as the fuel. The formation of single phase cubic spinel structure was confirmed by powder X-ray diffraction (XRD), Rietveld analysis and Fourier transform infrared (FT-IR) spectroscopy and the calculated average crystallite size is in the range of 37.57 nm to 25.43 nm. The high resolution scanning electron microscopy (HR-SEM) and high resolution transmission electron microscopy (HR-TEM) results indicated that the as-prepared spinel Mn(x)Zn(1-x)Fe2O4 NPs showed high crystallinity and uniform size distribution with particles-like morphologies. The energy dispersive X-ray (EDX) analysis was confirmed the elemental composition and purity of the samples. The estimated band gap energy from UV-Visible diffuse reflectance spectroscopy (UV-Vis. DRS) is about 1.88 eV to 2.35 eV. The broad visible emission band is observed in the entire photoluminescence (PL) spectroscopy for all compositions. The variation of magnetization (M(s)) value of the samples was studied by vibrating sample magnetometer (VSM) and the lower compositions (x = 0.0, 0.2 and 0.4) show a superparamagnetism and the higher composition (x = 0.6, 0.8 and 1.0) show a ferromagnetic behavior with hysteresis and that the M(s) values increased with increasing Mn2+ content to reach a maximum value of 60.99 emu/g for MnFe2O4. All composition of spinel Mn(x)Zn(1-x)Fe2O4 NPs were successfully tested as catalyst for the oxidation of benzyl alcohol into benzaldehyde, which has resulted 83.29 and 96.51% conversion efficiency of ZnFe2O4 and Mn0.6Zn0.4Fe2O4 respectively.
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