Iron hydroxide nanoparticles coated with poly(ethylene glycol)-poly(aspartic acid) block copolymer as novel magnetic resonance contrast agents for in vivo cancer imaging

被引:83
作者
Kumagai, Michiaki
Imai, Yutaka
Nakamura, Teisaku
Yamasaki, Yuichi
Sekino, Masaki
Ueno, Shoogo
Hanaoka, Kenjiro
Kikuchi, Kazuya
Nagano, Tetsuo
Kaneko, Eiji
Shimokado, Kentaro
Kataoka, Kazunori
机构
[1] Univ Tokyo, Sch Engn, Dept Mat Engn, Bunkyo Ku, Tokyo 1138656, Japan
[2] Tokyo Med & Dent Univ, Sch Med, Dept Vasc Med & Geriatr, Bunkyo Ku, Tokyo 1138519, Japan
[3] Univ Tokyo, Sch Med, Dept Biomed Engn, Bunkyo Ku, Tokyo 1130033, Japan
[4] Univ Tokyo, Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[5] Univ Tokyo, Sch Med, Ctr Dis Biol & Integrat Med, Bunkyo Ku, Tokyo 1130033, Japan
[6] Univ Tokyo, Ctr NanoBio Integrat, Bunkyo Ku, Tokyo 1138656, Japan
关键词
magnetic resonance imaging; tumor; contrast agent; beta-FeOOH; poly(ethylene glycol); block copolymer; zeta potential; FT-IR;
D O I
10.1016/j.colsurfb.2006.12.019
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
PEG-coated P-FeOOH nanoparticles were prepared through electrostatic complex formation of iron oxide nanoparticles with poly(ethylene glycol)-poly(aspartic acid) block copolymer [PEG-P(Asp)] in distilled water. By dynamic light scattering (DLS) measurement, the nanopaticle size was determined to be 70 nm with narrow distribution. The FT-IR and zeta potential experimental results proved that PEG-PAsp molecules bound to the surface of the iron oxide nanoparticles via the coordination between the carboxylic acid residues in the PAsp segment of the block copolymer and the surface Fe of the P-FeOOH nanoparticles. The PEG-coated nanoparticles revealed excellent solubility and stability in aqueous solution as well as in physiological saline. In vivo MRI experiments on tumor-bearing mice demonstrated that the PEG-coated nanoparticles prepared by the current approach achieved an appreciable accumulation into solid tumor, suggesting their potential utility as tumor-selective MRI contrast agents. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:174 / 181
页数:8
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