le Masne de Chermont Quentin, Chanéac Corinne, Seguin Johanne, Pellé Fabienne, Maîtrejean Serge, Jolivet Jean-Pierre, Gourier Didier, Bessodes Michel, Scherman Daniel
Institut National de la Santé et de la Recherche Médicale, Unité 640, F-75006 Paris, France.
Proc Natl Acad Sci U S A. 2007 May 29;104(22):9266-71. doi: 10.1073/pnas.0702427104. Epub 2007 May 21.
Fluorescence is increasingly used for in vivo imaging and has provided remarkable results. Yet this technique presents several limitations, especially due to tissue autofluorescence under external illumination and weak tissue penetration of low wavelength excitation light. We have developed an alternative optical imaging technique by using persistent luminescent nanoparticles suitable for small animal imaging. These nanoparticles can be excited before injection, and their in vivo distribution can be followed in real-time for more than 1 h without the need for any external illumination source. Chemical modification of the nanoparticles' surface led to lung or liver targeting or to long-lasting blood circulation. Tumor mass could also be identified on a mouse model.
荧光越来越多地用于体内成像,并取得了显著成果。然而,这项技术存在一些局限性,特别是由于外部照明下的组织自发荧光以及低波长激发光的组织穿透性较弱。我们通过使用适用于小动物成像的持续发光纳米颗粒开发了一种替代光学成像技术。这些纳米颗粒在注射前可以被激发,并且它们在体内的分布可以实时跟踪超过1小时,而无需任何外部照明源。纳米颗粒表面的化学修饰导致其靶向肺部或肝脏或实现长时间的血液循环。在小鼠模型上也可以识别出肿瘤块。