In Vivo HER2-Targeted Magnetic Resonance Tumor Imaging Using Iron Oxide Nanoparticles Conjugated with Anti-HER2 Fragment Antibody

被引:31
作者
Ding, Ning [1 ]
Sano, Kohei [1 ,2 ]
Kanazaki, Kengo [1 ,3 ]
Ohashi, Manami [1 ]
Deguchi, Jun [1 ]
Kanada, Yuko [1 ]
Ono, Masahiro [1 ]
Saji, Hideo [1 ]
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Dept Pathofunct Bioanal, Sakyo Ku, 46-29 Yoshida Shimoadachi Cho, Kyoto 6068501, Japan
[2] Kyoto Univ Hosp, Sakyo Ku, 54 Kawaharacho, Kyoto 6068507, Japan
[3] Canon Inc, Corp R&D Headquarters, Med Imaging Project, Ohta Ku, 3-30-2 Shimomaruko, Tokyo 1468501, Japan
关键词
Molecular MRI; Cancer imaging; Iron oxide nanoparticle; HER2; Single-chain Fv; GENE AMPLIFICATION; CONTRAST AGENTS; GASTRIC-CANCER; THERAPY; HYPERTHERMIA; CELLS; HER-2; MRI;
D O I
10.1007/s11307-016-0977-2
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
The feasibility of iron oxide nanoparticles (IONPs) conjugated with anti-epidermal growth factor receptor 2 (HER2) single-chain antibody (scFv-IONPs) as novel HER2-targeted magnetic resonance (MR) contrast agents was investigated. The scFv-IONPs were prepared and identified. For in vitro MRI, NCI-N87 (HER2 high expression) and SUIT2 (low expression) cells were incubated with scFv-IONPs. For in vivo MRI, NCI-N87 and SUIT2 tumor-bearing mice were intravenously injected with scFv-IONPs and imaged before and 24 h post-injection. The scFv-IONPs demonstrated high transverse relaxivity (296.3 s(-1) mM(-1)) and affinity toward HER2 (K-D = 11.7 nM). In the in vitro MRI, NCI-N87 cells treated with scFv-IONPs exhibited significant MR signal reduction (44.6 %) than SUIT2 cells (6.8 %). In the in vivo MRI, decrease of MR signals in NCI-N87 tumors (19.3 %) was more notable than that in SUIT2 tumors (6.2 %). The scFv-IONPs enabled HER2-specific tumor MR imaging, suggesting the potential of scFv-IONPs as a robust HER2-targeted MR contrast agent.
引用
收藏
页码:870 / 876
页数:7
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