Department of Medical Biochemistry, University of Shizuoka, Yada, Shizuoka 422-8526, Japan.
Int J Pharm. 2011 Jan 17;403(1-2):170-7. doi: 10.1016/j.ijpharm.2010.10.001. Epub 2010 Oct 8.
Since nanocarriers such as liposomes are known to accumulate in tumors of tumor-bearing animals, and those that have entrapped a positron emitter can be used to image a tumor by PET, we applied (18)F-labeled 100-nm-sized liposomes for the imaging of brain tumors. Polyethylene glycol (PEG)-modified liposomes, which are known to accumulate in tumors by passive targeting and those modified with Ala-Pro-Arg-Pro-Gly, which are known to home into angiogenic sites were used. Those liposomes labeled with DiI fluorescence accumulated in a glioma implanted in a rat brain 1h after the injection, although they did not accumulate in the normal brain tissues due to the protection afforded by the blood-brain barrier. Preformed liposomes were easily labeled with 1-[(18)F]fluoro-3,6-dioxatetracosane, and enabled the imaging of gliomas by PET with higher contrast than that obtained with [(18)F]deoxyfluoroglucose. In addition, the smallest tumor among those tested, having a diameter of 1mm was successfully imaged by the liposomal (18)F. Therefore, nanocarrier-based imaging of brain tumors is promising for the diagnosis of brain cancer and possible drug delivery-based therapy.
由于已知诸如脂质体的纳米载体在荷瘤动物的肿瘤中蓄积,并且那些包封了正电子发射体的纳米载体可以通过 PET 用于肿瘤成像,因此我们应用(18)F 标记的 100nm 大小的脂质体来对脑肿瘤进行成像。使用了聚乙二醇(PEG)修饰的脂质体,已知其通过被动靶向在肿瘤中蓄积,以及用 Ala-Pro-Arg-Pro-Gly 修饰的脂质体,已知其归巢到血管生成部位。用 DiI 荧光标记的那些脂质体在注射后 1 小时在大鼠脑内植入的神经胶质瘤中蓄积,尽管由于血脑屏障的保护作用,它们不会在正常脑组织中蓄积。预形成的脂质体很容易用 1-[(18)F]氟-3,6-二氧杂二十四烷标记,并且通过 PET 能够比用 [(18)F]脱氧氟葡萄糖获得更高对比度的神经胶质瘤成像。此外,在所测试的最小肿瘤中,直径为 1mm 的肿瘤成功地通过脂质体(18)F 成像。因此,基于纳米载体的脑肿瘤成像有望用于脑癌的诊断和可能的基于药物输送的治疗。