University of Central Florida, Department of Chemistry, P.O. Box 162366, Orlando, FL 32816-2366, USA.
Biomaterials. 2012 Nov;33(33):8477-85. doi: 10.1016/j.biomaterials.2012.06.082. Epub 2012 Aug 30.
We report the use of small molecule and block copolymer RGD peptide conjugates for deep ex vivo imaging of tumor vasculature in "whole" excised tumors using two-photon fluorescence microscopy (2PFM). The fluorescent probes were administered to mice via tail-vein injection, after which the tumors were excised, fixed, and imaged without further sample preparation. Both RGD conjugates demonstrated specific targeting to tumor blood vessels, and this selectivity imparted excellent contrast in 2PFM micrographs that captured high-resolution 3-D images of the tumor vasculature up to depths of 830 μm in Lewis Lung Carcinoma (LLC) tumors. 2PFM ex vivo fluorescence micrographs clearly revealed tumor vessels, while differences in the sensitivity of tumor vessel imaging were apparent between the small molecule and block copolymer conjugates. Both the small molecule and polymer-based two-photon absorbing probe conjugate are valuable for deep tissue tumor microvasculature imaging.
我们报告了小分子和嵌段共聚物 RGD 肽缀合物在使用双光子荧光显微镜(2PFM)对“完整”离体肿瘤中的肿瘤血管进行深层离体成像的应用。荧光探针通过尾静脉注射给予小鼠,然后切除、固定肿瘤,无需进一步的样品制备即可进行成像。两种 RGD 缀合物均特异性靶向肿瘤血管,这种选择性在 2PFM 显微照片中提供了出色的对比度,可捕获高达 830μm 深度的 Lewis 肺癌(LLC)肿瘤的高分辨率 3D 图像。2PFM 离体荧光显微照片清楚地显示了肿瘤血管,而小分子和嵌段共聚物缀合物在肿瘤血管成像的敏感性方面存在差异。小分子和基于聚合物的双光子吸收探针缀合物都可用于深层组织肿瘤微血管成像。