Preparation, biocompatibility and imaging performance of ultrasmall iron oxide magnetic fluids for T1/T2-weighted MRI

被引:8
|
作者
Li, Hongcai [1 ]
Wang, Rui [2 ]
Hong, Ruoyu [1 ]
Li, Yonggang [2 ]
机构
[1] Fuzhou Univ, Coll Chem Engn, Fuzhou 350108, Fujian, Peoples R China
[2] Soochow Univ, Med Coll, Suzhou 215006, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
MRI; Ultrasmall nanoparticles; Stability; Biocompatibility; Dual-modulus imaging; FE3O4; NANOPARTICLES; RENAL CLEARANCE; CONTRAST AGENT; DUAL CONTRAST; IN-VITRO; T-1; SIZE; NANOCRYSTALS;
D O I
10.1016/j.colsurfa.2022.129360
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In order to further improve the stability and biocompatibility of magnetic fluids (MFs), we report a one-step protocol for the preparation of ultrasmall superparamagnetic iron oxide MFs. Four kinds of MFs (n %LCysteine-S-branched polymethacrylic acid-coated Fe3O4 nanoparticles MFs, n %Cys-PMAA@Fe3O4 MFs) with ultrasmall particle size (< 5 nm) were obtained using the different molecular weight of polymer ligands as the outer layer. Among them, 2 %Cys-PMAA@Fe3O4 MFs show the best performance in the apparent particle size (4.10 +/- 0.90 nm), hydrodynamic size (< 50 nm), and magnetic weight gain (67 mg), and stability index (I = 99 %). In addition, 2 %Cys-PMAA@Fe3O4 MFs exhibit excellent stability for 180 days under different salt concentrations (up to 3 mol/L) and pH (2-12). Importantly, the 2 %Cys-PMAA@Fe3O4 MFs show good biocompatibility in vitro that HEK293T and MCF-7 cells viability are higher than 90 % in 24 h when the iron concentration is 250 mu g.mL(-1). Furthermore, the hemolysis test and H&E tissue section staining demonstrate that the MFs are non-toxic in vivo. Finally, the value of 2 %Cys-PMAA@Fe3O4 MFs at 1.5 T (r(2) = 57.48 mM(-1).s(-1), r(1) = 8.61 (-1).s(-1), r(2)/r(1) = 6.68) is slightly less than Combidex for r(2) (r(2) = 65 mM(-1).s(-1)), and 2.5-folds higher than Gd-DTPA for r(1) (r(1) = 3.5 mM(-1).s(-1)), so the tumor area can be clearly observed with dual-mode imaging at 3.0 T in vivo by the tail vein injection. This study contributes to the rationalized design and development of a clinical dual-modulus contrast agent.
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页数:9
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