Department of Diagnostic Radiology and Organ Imaging, Prince of Wales Hospital, Chinese University of Hong Kong, Shatin, NT, Hong Kong SAR, China.
J Magn Reson Imaging. 2010 Jun;31(6):1508-13. doi: 10.1002/jmri.22173.
To determine whether low-intensity pulsed ultrasound (LIPUS) is able to facilitate the uptake of a superparamagnetic iron oxide (SPIO) nanomaterial by cells that do not express high endocytosis capacity.
The human osteosarcoma cell line U2OS and a silica-coated SPIO functionalized peripherally with amines groups (overall diameter 8 nm) were used in this study. Adherent U2OS cells were labeled with SPIO by incubating with culture media containing the SPIO at 4.5 microg[Fe]/mL. LIPUS with the same parameters as those used in clinical application to accelerate bone fracture healing (1.5 MHz, duty cycle 1:4, spatial-average temporal-average intensity 30 mW/cm(2)) was applied to the cells at the beginning of the labeling process for 0, 0.5, 1, or 3 hours. The total incubation time with SPIO was 12 hours. SPIO labeling efficiency was evaluated with Prussian blue staining and a blueness measurement method, and magnetic resonance imaging (MRI) of cell pellets via measuring areas of SPIO-induced signal void.
Both Prussian blue staining and in vitro MRI demonstrated that LIPUS application increased the SPIO nanomaterial labeling efficiency for U2OS cells in an exposure-duration-dependent manner.
This study is a "proof of concept" that LIPUS can facilitate the cellular take-up of SPIO nanomaterial.
确定低强度脉冲超声(LIPUS)是否能够促进细胞摄取超顺磁氧化铁(SPIO)纳米材料,而这些细胞不表达高内吞能力。
本研究使用人骨肉瘤细胞系 U2OS 和一种经过胺基基团修饰的二氧化硅包裹的 SPIO(总直径 8nm)。附着的 U2OS 细胞通过在含有 4.5μg[Fe]/mL SPIO 的培养基中孵育来标记 SPIO。LIPUS 以与临床应用加速骨折愈合相同的参数(1.5MHz,占空比 1:4,空间平均时间平均强度 30mW/cm(2))在标记过程开始时应用于细胞 0、0.5、1 或 3 小时。SPIO 的总孵育时间为 12 小时。通过普鲁士蓝染色和蓝色测量方法评估 SPIO 标记效率,并通过测量 SPIO 诱导的信号缺失区域对细胞沉淀进行磁共振成像(MRI)。
普鲁士蓝染色和体外 MRI 均表明,LIPUS 应用以暴露时间依赖的方式增加了 U2OS 细胞中 SPIO 纳米材料的标记效率。
这项研究是“概念验证”,表明 LIPUS 可以促进细胞摄取 SPIO 纳米材料。