Herein, nanocrystalline MoB(2) powder synthesized via a single-step molten salt reaction of precursor materials MoCl(5) and amorphous boron powder in the presence of KCl and NaCl by varying the boron amount was applied for the first time in vitro cytotoxicity and antibacterial studies. The crystalline structure, morphology, and surface characteristics were investigated in detail by powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), and Brunauer-Emmett-Teller (BET) analysis. The results indicated that the amount of boron played a crucial role in the nanostructure of MoB(2). XRD results showed an enhancement in crystallinity, and HRTEM examinations revealed a rise in reflections (100) and growth in grains with the rise in boron amount during the synthesis of MoB(2). The particle size was found to be in the range of 50-100 nm, and the surface areas of MoB(2) nanoparticles were measured between 7.74 and 16.11 m(2)/g. In vitro findings showed that MoB(2)-16 did not have a significant cytotoxic effect on healthy cells (HaCaT and MCF10A), but it exhibited a notable cytotoxic effect on breast cancer cell lines (MDA-MB-231 and MCF7 cells), whereas no cytotoxic effect occurred on the liver cancer line Hep3B cells. Antibacterial studies revealed that MoB(2)-4 exhibited promising antibacterial activity against both S. aureus and E. coli, where MICs were in the range of 60 to 70 μg/mL. Overall, our research reported the successful synthesis and characterization of MoB(2) nanoparticles, which can be efficient anticancer and antibacterial agents.
Molybdenum Diboride (MoB(2)) Nanoparticles via a Facile Molten Salt Route: Synthesis, Characterization, Cytotoxicity, and Antibacterial Studies.
通过简便的熔盐法制备二硼化钼(MoB(2))纳米粒子:合成、表征、细胞毒性和抗菌研究
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作者:Aydın Hamide, Ãstün Burcu, Åahintürk Utkan, DeÄirmenci Nurdan Sena, Åahin Fikrettin, Kaptan Usul Sedef, Aslan AyÅe, Demir Muslum, Kurtan Ãmran
| 期刊: | ACS Applied Bio Materials | 影响因子: | 4.700 |
| 时间: | 2025 | 起止号: | 2025 Aug 18; 8(8):6745-6754 |
| doi: | 10.1021/acsabm.5c00161 | 研究方向: | 细胞生物学 |
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