Minematsu Hideki, Otani Takayuki, Oohashi Toshitaka, Hirai Masahiko, Oie Kazunori, Igarashi Koichi, Ohtsuka Aiji
Katayama Chemical Industries Co. Ltd., R&D Division, Minoh, Osaka 562-0015, Japan.
J Electron Microsc (Tokyo). 2011;60(1):95-9. doi: 10.1093/jmicro/dfq071. Epub 2010 Oct 5.
Active targeting of the liposome is an attractive strategy for drug delivery and in vivo bio-imaging. We previously reported the specific accumulation of Sialyl Lewis X (SLX) liposome to inflamed tissue in arthritic model mice or tumor-bearing mice. SLX-liposome encapsulation with fluorescent substances allows for the visualization of these liposomes by the time-dependent transvascular accumulation of fluorescent signals in the histological sections. In the present study, we developed a new SLX-liposome encapsulated with colloidal gold for transmission electron microscopic observation. We herein describe the characterization of the colloidal gold-loaded SLX-liposomes and demonstrate its specific targeting to the endothelial cells of tumor blood vessels in tumor-bearing mice.
脂质体的主动靶向是一种用于药物递送和体内生物成像的有吸引力的策略。我们之前报道了唾液酸化路易斯X(SLX)脂质体在关节炎模型小鼠或荷瘤小鼠的炎症组织中的特异性积累。用荧光物质包封SLX脂质体可通过组织学切片中荧光信号随时间的跨血管积累来实现这些脂质体的可视化。在本研究中,我们开发了一种包封有胶体金的新型SLX脂质体用于透射电子显微镜观察。我们在此描述了负载胶体金的SLX脂质体的特性,并证明了其对荷瘤小鼠肿瘤血管内皮细胞的特异性靶向。