Cinar-Acar Berat
Faculty of Science, Department of Biology, Gazi University, 906500, Ankara, Turkey.
Sci Rep. 2025 Jul 16;15(1):25875. doi: 10.1038/s41598-025-09192-8.
The limitations of both inorganic and organic selenium sources, such as low bioavailability and potential toxicity, have driven research towards selenium nanoparticles (SeNPs). In this study, β-glucan was extracted from the cell wall of Kluyveromyces marxianus M59 and subsequently carboxymethylated to enhance its water solubility. Carboxymethylated β-glucan was then utilized for the synthesis of selenium nanoparticles (SeNPs), and their sizes were determined using Scanning Electron Microscopy (SEM) analysis. To reduce the size of larger nanoparticles, Cold Atmospheric Plasma (CAP) treatment was applied, resulting in an approximately 82.4% decrease in particle size. The SeNPs obtained ranged in size from 180 to 83 nm. The synthesized SeNPs were characterized using UV-Vis Spectrophotometry, Fourier-Transform Infrared Spectroscopy (FTIR), and X-ray Diffraction (XRD) analysis. The absorption peak of SeNPs was detected at 330 nm, further confirming their amorphous nature. Additionally, the biological activities of SeNPs, including their antimicrobial, antibiofilm, and antioxidant properties, were investigated. When the antibiofilm activity of SeNPs was evaluated, the highest inhibition rate (43.6 ± 0.1%) was observed at a concentration of 5 mg/mL. In contrast, regarding antimicrobial activity, SeNPs exhibited limited inhibition zones at low concentrations, with a maximum inhibition diameter of 1.20 mm recorded. Antioxidant activity was evaluated through 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging, superoxide anion scavenging, and hydroxyl radical scavenging assays. The highest antioxidant activity was determined at 5 mg/mL SeNP concentration (47.7%) at DPPH method. The cytotoxic effects of SeNPs were evaluated on both healthy (L929) and lung cancer (A549) cell lines. The IC for L929 cells remained above 200 µg/mL (411 and 390 µg/mL) at both hours (24 and 48 h), whereas in A549 cells, it was approximately 65 µg/mL at 24 h and 34 µg/mL at 48 h. In this study, SeNPs whose particle sizes were reduced through the CAP process were found to exhibit antibiofilm, antioxidant, and non-toxic properties, suggesting their potential for sustainable and different applications such as healthcare, biomaterials, environmental protection, and drug delivery. The findings of this study provide preliminary insights that will guide future research aimed at elucidating the molecular mechanisms of SeNPs, optimising their biocompatibility and targeted applications, integrating them into advanced biomedical and environmental systems, and evaluating their potential for sustainable use.
无机和有机硒源都存在局限性,如生物利用度低和潜在毒性,这推动了对硒纳米颗粒(SeNPs)的研究。在本研究中,从马克斯克鲁维酵母M59的细胞壁中提取β-葡聚糖,随后进行羧甲基化以提高其水溶性。然后将羧甲基化的β-葡聚糖用于合成硒纳米颗粒(SeNPs),并使用扫描电子显微镜(SEM)分析确定其尺寸。为了减小较大纳米颗粒的尺寸,应用了冷大气等离子体(CAP)处理,导致颗粒尺寸减少了约82.4%。获得的SeNPs尺寸范围为180至83nm。使用紫外-可见分光光度法、傅里叶变换红外光谱(FTIR)和X射线衍射(XRD)分析对合成的SeNPs进行了表征。在330nm处检测到SeNPs的吸收峰,进一步证实了它们的无定形性质。此外,还研究了SeNPs的生物活性,包括其抗菌、抗生物膜和抗氧化特性。在评估SeNPs的抗生物膜活性时,在浓度为5mg/mL时观察到最高抑制率(43.6±0.1%)。相比之下,关于抗菌活性,SeNPs在低浓度下表现出有限的抑菌圈,记录到的最大抑菌直径为1.20mm。通过1,1-二苯基-2-苦基肼(DPPH)自由基清除、超氧阴离子清除和羟基自由基清除试验评估抗氧化活性。在DPPH法中,在SeNP浓度为5mg/mL时测定到最高抗氧化活性(47.7%)。在健康(L929)和肺癌(A549)细胞系上评估了SeNPs的细胞毒性作用。在两个时间点(24小时和48小时),L929细胞的IC均保持在200μg/mL以上(411和390μg/mL),而在A549细胞中,24小时时约为65μg/mL,48小时时约为34μg/mL。在本研究中,发现通过CAP工艺减小粒径的SeNPs具有抗生物膜、抗氧化和无毒特性,表明它们在医疗保健、生物材料、环境保护和药物递送等可持续和不同应用方面具有潜力。本研究的结果提供了初步见解,将指导未来旨在阐明SeNPs分子机制、优化其生物相容性和靶向应用、将它们整合到先进的生物医学和环境系统中以及评估其可持续利用潜力的研究。