Răcuciu Mihaela, Oancea Simona, Barbu-Tudoran Lucian, Drăghici Olga, Agavriloaei Anda, Creangă Dorina
Environmental Sciences and Physics Department, Faculty of Sciences, Lucian Blaga University of Sibiu, Dr. I. Ratiu Str., no. 5-7, 550012 Sibiu, Romania.
Agricultural Sciences and Food Engineering Department, Lucian Blaga University of Sibiu, Dr. I. Ratiu Str., no. 7-9, 550012 Sibiu, Romania.
Materials (Basel). 2024 Mar 7;17(6):1229. doi: 10.3390/ma17061229.
Hyaluronic acid (HA) has attracted much attention in tumor-targeted drug delivery due to its ability to specifically bind to the CD44 cellular receptor, which is widely expressed on cancer cells. We present HA-capped magnetic nanoparticles (HA-MNPs) obtained via the co-precipitation method, followed by the electrostatic adsorption of HA onto the nanoparticles' surfaces. A theoretical study carried out with the PM3 method evidenced a dipole moment of 3.34 D and negatively charged atom groups able to participate in interactions with nanoparticle surface cations and surrounding water molecules. The ATR-FTIR spectrum evidenced the hyaluronic acid binding to the surface of the ferrophase, ensuring colloidal stability in the water dispersion. To verify the success of the synthesis and stabilization, HA-MNPs were also characterized using other investigation techniques: TEM, EDS, XRD, DSC, TG, NTA, and VSM. The results showed that the HA-MNPs had a mean physical size of 9.05 nm (TEM investigation), a crystallite dimension of about 8.35 nm (XRD investigation), and a magnetic core diameter of about 8.31 nm (VSM investigation). The HA-MNPs exhibited superparamagnetic behavior, with the magnetization curve showing saturation at a high magnetic field and a very small coercive field, corresponding to the net dominance of single-domain magnetic nanoparticles that were not aggregated with reversible magnetizability. These features satisfy the requirement for magnetic nanoparticles with a small size and good dispersibility for long-term stability. We performed some preliminary tests regarding the nanotoxicity in the environment, and some chromosomal aberrations were found to be induced in corn root meristems, especially in the anaphase and metaphase of mitotic cells. Due to their properties, HA-MNPs also seem to be suitable for use in the biomedical field.
透明质酸(HA)因其能够特异性结合广泛表达于癌细胞上的CD44细胞受体,在肿瘤靶向给药方面备受关注。我们展示了通过共沉淀法获得的HA包覆磁性纳米颗粒(HA-MNPs),随后通过静电吸附将HA吸附到纳米颗粒表面。用PM3方法进行的理论研究表明,其偶极矩为3.34 D,且存在带负电荷的原子基团,能够参与与纳米颗粒表面阳离子及周围水分子的相互作用。ATR-FTIR光谱证明了透明质酸与铁相表面的结合,确保了水分散体中的胶体稳定性。为验证合成和稳定化的成功,还使用其他研究技术对HA-MNPs进行了表征:透射电子显微镜(TEM)、能谱分析(EDS)、X射线衍射(XRD)、差示扫描量热法(DSC)、热重分析法(TG)、纳米颗粒跟踪分析(NTA)和振动样品磁强计(VSM)。结果表明,HA-MNPs的平均物理尺寸为9.05 nm(TEM研究),微晶尺寸约为8.35 nm(XRD研究),磁芯直径约为8.31 nm(VSM研究)。HA-MNPs表现出超顺磁性行为,磁化曲线在高磁场下显示饱和,矫顽场非常小,这对应于未聚集且具有可逆磁化性的单畴磁性纳米颗粒的净主导地位。这些特性满足了对尺寸小、分散性好且长期稳定的磁性纳米颗粒的要求。我们对环境中的纳米毒性进行了一些初步测试,发现玉米根尖分生组织中诱导了一些染色体畸变,尤其是在有丝分裂细胞的后期和中期。由于其特性,HA-MNPs似乎也适用于生物医学领域。