Hu Fengqin, MacRenaris Keith W, Waters Emily A, Liang Taiyang, Schultz-Sikma Elise A, Eckermann Amanda L, Meade Thomas J
Department of Chemistry, Biochemistry, Molecular Biology and Cell Biology, Neurobiology and Physiology, Radiology, Northwestern University, Evanston, Illinois 60208.
J Phys Chem C Nanomater Interfaces. 2009 Dec 10;113(49):20855-20860. doi: 10.1021/jp907216g.
Ultrasmall (3, 4, 5, and 6 nm), water-soluble FeO magnetic nanoparticles were synthesized in diethylene glycol (DEG) via a facile one-pot reaction. Hydrodynamic size and relaxation time measurements did not show particle aggregation when FeO nanoparticles were dispersed in phosphate buffered saline, fetal bovine serum, or calf bovine serum for 1 week. Furthermore, the new FeO nanoparticles tolerated high salt concentrations (≤1 M NaCl) and a wide pH range from 5 to 11. Surface modification of the nanoparticles with poly(ethylene glycol) bis(carboxymethyl) ether (HOOC-PEG-COOH, 600 g/mol) was accomplished through a ligand-exchange reaction. The effects of PEG modification on magnetization and relaxivity of the FeO nanoparticles were investigated, and the results indicate that the increase in transverse relaxivity after PEG modification may be due to the increased volume of slowly diffusing water surrounding each nanoparticle. In vitro experiments showed that the DEG- and PEG-coated FeO nanoparticles have little effect on NIH/3T3 cell viability.
通过简便的一锅法反应,在二甘醇(DEG)中合成了超小(3、4、5和6纳米)的水溶性FeO磁性纳米颗粒。当FeO纳米颗粒分散在磷酸盐缓冲盐水、胎牛血清或小牛血清中1周时,流体动力学尺寸和弛豫时间测量未显示颗粒聚集。此外,新型FeO纳米颗粒耐受高盐浓度(≤1 M NaCl)以及5至11的宽pH范围。通过配体交换反应,用聚(乙二醇)双(羧甲基)醚(HOOC-PEG-COOH,600 g/mol)对纳米颗粒进行表面修饰。研究了PEG修饰对FeO纳米颗粒磁化强度和弛豫率的影响,结果表明PEG修饰后横向弛豫率的增加可能是由于每个纳米颗粒周围缓慢扩散的水体积增加所致。体外实验表明,DEG和PEG包覆的FeO纳米颗粒对NIH/3T3细胞活力影响很小。