Mora-Cabello Romualdo, Fuentes-Ríos David, Gago Lidia, Cabeza Laura, Moscoso Ana, Melguizo Consolación, Prados José, Sarabia Francisco, López-Romero Juan Manuel
Department of Organic Chemistry, Faculty of Sciences, University of Málaga, 29071 Málaga, Spain.
Institute of Biopathology and Regenerative Medicine (IBIMER), Biomedical Research Center (CIBM), 18100 Granada, Spain.
Pharmaceutics. 2024 Sep 19;16(9):1226. doi: 10.3390/pharmaceutics16091226.
: Magnetic FeO nanoparticles (MNPs) are becoming more important every day. We prepared MNPs in a simple one-step reaction by following the solvothermal method, assisted by azide and alkyne functionalized polyethylene glycol (PEG400) polymers, as well as by PEG6000 and the polyol β-cyclodextrin (βCD), which played a crucial role as electrostatic stabilizers, providing polymeric/polyol coatings around the magnetic cores. : The composition, morphology, and magnetic properties of the nanospheres were analyzed using Transmission Electron and Atomic Force Microscopies (TEM, AFM), Nuclear Magnetic Resonance (NMR), X-ray Diffraction Diffractometry (XRD), Fourier-Transform Infrared Spectroscopy (FT-IR), Matrix-Assisted Laser Desorption/Ionization (MALDI) and Vibrating Sample Magnetometry (VSM). : The obtained nanoparticles (@FeO-PEGs and @FeO-βCD) showed diameters between 90 and 250 nm, depending on the polymer used and the FeO·6HO precursor concentration, typically, 0.13 M at 200 °C and 24 h of reaction. MNPs exhibited superparamagnetism with high saturation mass magnetization at room temperature, reaching values of 59.9 emu/g (@FeO-PEG6000), and no ferromagnetism. Likewise, they showed temperature elevation after applying an alternating magnetic field (AMF), obtaining Specific Absorption Rate (SAR) values of up to 51.87 ± 2.23 W/g for @FeO-PEG6000. Additionally, the formed systems are susceptible to click chemistry, as was demonstrated in the case of the cannabidiol-propargyl derivative (CBD-Pro), which was synthesized and covalently attached to the azide functionalized surface of @FeO-PEG400-N. Prepared MNPs are highly dispersible in water, PBS, and citrate buffer, remaining in suspension for over 2 weeks, and non-toxic in the T84 human colon cancer cell line, : indicating that they are ideal candidates for biomedical applications.
磁性FeO纳米颗粒(MNPs)正日益重要。我们通过溶剂热法,在叠氮化物和炔烃功能化聚乙二醇(PEG400)聚合物以及PEG6000和多元醇β-环糊精(βCD)的辅助下,以简单的一步反应制备了MNPs,它们作为静电稳定剂发挥了关键作用,在磁核周围提供聚合物/多元醇涂层。
使用透射电子显微镜和原子力显微镜(TEM、AFM)、核磁共振(NMR)、X射线衍射衍射仪(XRD)、傅里叶变换红外光谱(FT-IR)、基质辅助激光解吸/电离(MALDI)和振动样品磁强计(VSM)对纳米球的组成、形态和磁性进行了分析。
所获得的纳米颗粒(@FeO-PEGs和@FeO-βCD)的直径在90至250nm之间,这取决于所使用的聚合物和FeO·6H₂O前驱体浓度,通常在200°C和24小时反应时为0.13M。MNPs在室温下表现出超顺磁性,具有高饱和质量磁化强度,达到59.9emu/g(@FeO-PEG6000),且无铁磁性。同样,在施加交变磁场(AMF)后它们会升温,@FeO-PEG6000的比吸收率(SAR)值高达51.87±2.23W/g。此外,所形成的体系易于进行点击化学,大麻二酚-炔丙基衍生物(CBD-Pro)的情况就证明了这一点,它被合成并共价连接到@FeO-PEG400-N的叠氮化物功能化表面。制备的MNPs在水、磷酸盐缓冲盐水(PBS)和柠檬酸盐缓冲液中具有高度分散性,可在悬浮状态下保持超过2周,并且在T84人结肠癌细胞系中无毒,
表明它们是生物医学应用的理想候选物。