Department of Biochemistry, Indian Institute of Science, Bangalore, 560012, India.
Laboratory of Functional Molecules and Materials, School of Physics and Optoelectronic Engineering, Shandong University of Technology, 255000, Xincun West Road 266, Zibo, China.
Appl Biochem Biotechnol. 2021 Dec;193(12):3983-3995. doi: 10.1007/s12010-021-03674-x. Epub 2021 Sep 20.
The present study highlights/demonstrates facile synthesis of β-Glucan nanoparticles (β-GluNPs) that can be used in the prevention of breast cancer and other infectious diseases. Moreover, this method is inexpensive and shows effectivity towards different biological applications. Further, the characterization of synthesized β-GluNPs was exclusively confirmed through UV-Vis spectroscopy, Fourier transform infrared spectroscopy (FT-IR), dynamic light scattering (DLS), zeta potential, scanning electron microscopy (SEM), high resolution-transmission electron microscopy (HR-TEM), and X-ray powder diffraction (XRD) analysis. The synthesized β-GluNPs were further confirmed by FT-IR spectroscopy. The HR-TEM results demonstrated that the formation of polydispersed nanoparticles with a mean size of 20 ± 5 nm. The hydrostatic zeta potential was - 22.7 mV, which indicated their colloidal stability. The XRD pattern revealed the crystalline nature of the nanoparticles. Besides, β-GluNPs showed better antibacterial activity against the tested pathogens. The apoptosis and DNA fragmentation observed to be IC 42.5 µg/ml of the β-GluNPs. The DNA fragmentation assay indicated the selective inhibition of the MCF-7 cell line by DNA damage. Hence, the study reports that the β-GluNPs have a potential to be used as a promising alternative drug against human breast cancer.
本研究强调/展示了β-葡聚糖纳米粒子(β-GluNPs)的简便合成方法,可用于预防乳腺癌和其他传染病。此外,这种方法成本低廉,对不同的生物应用具有有效性。进一步,通过紫外-可见光谱、傅里叶变换红外光谱(FT-IR)、动态光散射(DLS)、Zeta 电位、扫描电子显微镜(SEM)、高分辨率透射电子显微镜(HR-TEM)和 X 射线粉末衍射(XRD)分析专门确认了合成的β-GluNPs 的特性。通过傅里叶变换红外光谱进一步确认了合成的β-GluNPs。HR-TEM 结果表明,形成了具有平均尺寸为 20±5nm 的多分散纳米粒子。静水 Zeta 电位为-22.7mV,表明其胶体稳定性。XRD 图谱显示了纳米粒子的结晶性质。此外,β-GluNPs 对测试病原体表现出更好的抗菌活性。观察到凋亡和 DNA 片段化的 IC42.5μg/ml 的β-GluNPs。DNA 片段化分析表明β-GluNPs 对 MCF-7 细胞系的选择性抑制作用是通过 DNA 损伤引起的。因此,该研究报告称,β-GluNPs 具有作为治疗人类乳腺癌的有前途的替代药物的潜力。