Accumulation of liposome with Sialyl Lewis X to inflammation and tumor region:: Application to in vivo bio-imaging

被引:90
作者
Hirai, Masahiko [1 ]
Minematsu, Hideki [1 ]
Kondo, Naoko [1 ]
Oie, Kazunori [1 ]
Igarashi, Koichi [1 ]
Yamazaki, Noboru [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Nanotechnol Res Inst, Ibaraki 3058565, Japan
关键词
liposome; sugar chain; in vivo bio-imaging; Sialyl Lewis X; inflammation; drug delivery system;
D O I
10.1016/j.bbrc.2006.12.060
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We prepared the liposome binding Sialyl Lewis X (SLX) on the surface in order to specifically and efficiently deliver substances (fluorescent materials, chemical substances, proteins, genes, etc.) to inflammation or tumor regions. The liposome with SLX (SLX-Lipo-Cy5.5), in which fluorescent substance Cy5.5 was included, was administered intravenously to arthritis or Ehrlich Ascites Tumor (EAT) bearing mouse, and the accumulation of liposome was observed using two types of in vivo fluorescent imaging equipment. The result was that the accumulation of SLX-Lipo-Cy5.5 to inflammation or tumor regions was significantly higher than the control liposome without sugar chain (Lipo-Cy5.5) at 24 and 48 It after administration. In addition, it was confirmed that this accumulation showed a shift of liposome from blood vessels to the surrounding tissues. Thus, it was proven that this liposome is useful not only as an in vivo bio-imaging reagent but also as a drug delivery system (DDS). (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:553 / 558
页数:6
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