Preparation and in vivo imaging of PEG-poly(L-lysine)-based polymeric micelle MRI contrast agents

被引:103
作者
Shiraishi, Kouichi [1 ]
Kawano, Kumi [2 ]
Minowa, Takuya [2 ]
Maitani, Yoshie [2 ]
Yokoyama, Masayuki [1 ]
机构
[1] Kanagawa Acad Sci & Technol, Yokoyama Nanomed Polymers Project, Takatsu Ku, Kanagawa 2130012, Japan
[2] Hoshi Univ, Inst Med Chem, Shinagawa Ku, Tokyo 1428501, Japan
关键词
Polymeric micelle; MRI contrast agent; Long circulation; Tumor imaging; Poly(ethylene glycol)-b-poly(L-lysine); BLOCK-COPOLYMER; DRUG-DELIVERY; ACID;
D O I
10.1016/j.jconrel.2009.01.010
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A polymeric micelle drug carrier system was applied to the targeting of an MRI (magnetic resonance imaging) contrast agent. A block copolymer, PEG-b-poly(L-lysine), was used for conjugation of gadolinium ions through chelating moieties, DOTA. The DOTA moieties were successfully conjugated to all primary amine groups of the lysine residues. The obtained block copolymer, PEG-b-poly(L-lysine-DOTA), formed a polymeric micelle. The polymeric micelle structure was maintained even after partial gadolinium chelation (similar to 40%) to the DOTA moieties. The prepared polymeric micelle MRI contrast agent was injected into a mouse tail vein at a dose of 0.05 mmol Gd/kg. The polymeric micelle-based MRI contrast agent exhibited stable blood circulation. A considerable amount (6.1 +/- 0.3% of ID/g of the polymeric micelle) was found to accumulate at solid tumors 24 h after intravenous injection by means of the EPR effect. An MRI analysis revealed that the signal intensity of the tumor was enhanced 2.0-fold by the use of this contrast agent. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:14 / 20
页数:7
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