Department of Experimental Molecular Imaging, RWTH Aachen University, Aachen, Germany.
Biomaterials. 2011 Sep;32(25):5863-71. doi: 10.1016/j.biomaterials.2011.04.056. Epub 2011 May 24.
Riboflavin is an essential vitamin for cellular metabolism and is highly upregulated in metabolically active cells. Consequently, targeting the riboflavin carrier protein (RCP) may be a promising strategy for labeling cancer and activated endothelial cells. Therefore, Ultrasmall SuperParamagnetic Iron Oxide nanoparticles (USPIO) were adsorptively coated with the endogenous RCP ligand flavin mononucleotide (FMN), which renders them target-specific and fluorescent. The core diameter, surface morphology and surface coverage of the resulting FMN-coated USPIO (FLUSPIO) were evaluated using a variety of physico-chemical characterization techniques (TEM, DLS, MRI and fluorescence spectroscopy). The biocompatibility of FLUSPIO was confirmed using three different cell viability assays (Trypan blue staining, 7-AAD staining and TUNEL). In vitro evaluation of FLUSPIO using MRI and fluorescence microscopy demonstrated high labeling efficiency of cancer cells (PC-3, DU-145, LnCap) and activated endothelial cells (HUVEC). Competition experiments (using MRI and ICP-MS) with a 10- and 100-fold excess of free FMN confirmed RCP-specific uptake of the FLUSPIO by PC-3 cells and HUVEC. Hence, RCP-targeting via FMN may be an elegant way to render nanoparticles fluorescent and to increase the labeling efficacy of cancer and activated endothelial cells. This was shown for FLUSPIO, which due to their high T(2)-relaxivity, are favorably suited for MR cell tracking experiments and cancer detection in vivo.
核黄素是细胞代谢所必需的维生素,在代谢活跃的细胞中高度上调。因此,靶向核黄素载体蛋白(RCP)可能是标记癌症和活化内皮细胞的一种有前途的策略。因此,超顺磁性氧化铁纳米颗粒(USPIO)被内源性 RCP 配体黄素单核苷酸(FMN)吸附性涂层,使其具有靶向性和荧光性。使用各种物理化学特性描述技术(TEM、DLS、MRI 和荧光光谱)评估了所得 FMN 涂层 USPIO(FLUSPIO)的核心直径、表面形态和表面覆盖率。通过三种不同的细胞活力测定法(台盼蓝染色、7-AAD 染色和 TUNEL)证实了 FLUSPIO 的生物相容性。使用 MRI 和荧光显微镜对 FLUSPIO 的体外评估表明,癌细胞(PC-3、DU-145、LnCap)和活化内皮细胞(HUVEC)的标记效率很高。使用 MRI 和 ICP-MS 进行的竞争实验(使用 10 倍和 100 倍过量的游离 FMN)证实了 FLUSPIO 通过 PC-3 细胞和 HUVEC 的 RCP 特异性摄取。因此,通过 FMN 进行 RCP 靶向可能是使纳米颗粒荧光化并提高癌症和活化内皮细胞标记效率的一种巧妙方法。这在 FLUSPIO 中得到了证明,由于其高 T(2)弛豫率,非常适合用于 MR 细胞跟踪实验和体内癌症检测。