Antibiofouling polymer-coated superparamagnetic iron oxide nanoparticles as potential magnetic resonance contrast agents for in vivo cancer imaging

被引:527
作者
Lee, Haerim
Lee, Eunhye
Kim, Do Kyung
Jang, Nam Kyu
Jeong, Yong Yeon
Jon, Sangyong
机构
[1] Gwangju Inst Sci & Technol, Dept Life Sci, Kwangju 500712, South Korea
[2] Keele Univ, Inst Sci & Technol Med, Stoke On Trent ST4 7QB, Staffs, England
[3] Chonnam Natl Univ, Sch Med, Dept Diagnost Radiol, Kwangju 501746, South Korea
关键词
D O I
10.1021/ja061529k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the fabrication and characterization of antifouling polymer-coated magnetic nanoparticles as nanoprobes for magnetic resonance ( MR) contrast agents. Magnetite superparamagnetic iron oxide nanoparticles ( SPION) were coated with the protein- or cell-resistant polymer, poly( TMSMA-r-PEGMA), to generate stable, protein- resistant MR probes. Coated magnetic nanoparticles synthesized using two different preparation methods ( in situ and stepwise, respectively) were both well dispersed in PBS buffer at a variety of pH conditions ( pH 1-10). In addition, dynamic light scattering data revealed that their sizes were not altered even after 24 h of incubation in 10% serum containing cell culture medium, indicative of a lack of protein adsorption on their surfaces. When the antibiofouling polymer-coated SPION were incubated with macrophage cells, uptake was significantly lower in comparison to that of the popular contrast agent, Feridex I. V., suggesting that the polymer-coated SPION can be long-circulated in plasma by escaping from uptake by the reticular endothelial system ( RES) such as macrophages. Indeed, when the coated SPION were administered to tumor xenograft mice by intravenous injection, the tumor could be detected in T2-weighted MR images within 1 h as a result of the accumulation of the nanomagnets within the tumor site. Although the poly( TMSMA-r-PEGMA)-coated SPION do not have any targeting ligands on their surface, they are potentially useful for cancer diagnosis in vivo.
引用
收藏
页码:7383 / 7389
页数:7
相关论文
共 60 条
[1]   Insights into the use of paramagnetic Gd(III) complexes in MR-molecular imaging investigations [J].
Aime, S ;
Cabella, C ;
Colombatto, S ;
Crich, SG ;
Gianolio, E ;
Maggioni, F .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2002, 16 (04) :394-406
[2]   Characterization of biophysical and metabolic properties of cells labeled with superparamagnetic iron oxide nanoparticles and transfection agent for cellular MR imaging [J].
Arbab, AS ;
Bashaw, LA ;
Miller, BR ;
Jordan, EK ;
Lewis, BK ;
Kalish, H ;
Frank, JA .
RADIOLOGY, 2003, 229 (03) :838-846
[3]   Molecular magnetic resonance imaging with targeted contrast agents [J].
Artemov, D .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2003, 90 (03) :518-524
[4]  
Baghi M, 2005, ANTICANCER RES, V25, P3665
[5]   Iron oxide-enhanced MR lymphography: initial experience [J].
Bellin, MF ;
Beigelman, C ;
Precetti-Morel, S .
EUROPEAN JOURNAL OF RADIOLOGY, 2000, 34 (03) :257-264
[6]   Superparamagnetic agents: Physicochemical characteristics and preclinical imaging evaluation [J].
Benderbous, S ;
Corot, C ;
Jacobs, P ;
Bonnemain, B .
ACADEMIC RADIOLOGY, 1996, 3 :S292-S294
[7]   Cell response to dextran-derivatised iron oxide nanoparticles post internalisation [J].
Berry, CC ;
Wells, S ;
Charles, S ;
Aitchison, G ;
Curtis, ASG .
BIOMATERIALS, 2004, 25 (23) :5405-5413
[8]  
Blasberg RG, 2003, MOL CANCER THER, V2, P335
[9]   Superparamagnetic agents in magnetic resonance imaging: Physicochemical characteristics and clinical applications - A review [J].
Bonnemain, B .
JOURNAL OF DRUG TARGETING, 1998, 6 (03) :167-174
[10]   T1 and T2 relaxometry of monocrystalline iron oxide nanoparticles (MION-46L): Theory and experiment [J].
Bulte, JWM ;
Brooks, RA ;
Moskowitz, BM ;
Bryant, LH ;
Frank, JA .
ACADEMIC RADIOLOGY, 1998, 5 :S137-S140