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低强度脉冲超声增强超顺磁性氧化铁纳米材料的细胞摄取:来自人骨肉瘤细胞系 U2OS 的结果。

Low-intensity pulsed ultrasound increases cellular uptake of superparamagnetic iron oxide nanomaterial: results from human osteosarcoma cell line U2OS.

机构信息

Department of Diagnostic Radiology and Organ Imaging, Prince of Wales Hospital, Chinese University of Hong Kong, Shatin, NT, Hong Kong SAR, China.

出版信息

J Magn Reson Imaging. 2010 Jun;31(6):1508-13. doi: 10.1002/jmri.22173.

Abstract

PURPOSE

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.

MATERIALS AND METHODS

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.

RESULTS

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.

CONCLUSION

This study is a "proof of concept" that LIPUS can facilitate the cellular take-up of SPIO nanomaterial.

摘要

目的

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。

材料与方法

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)。

结果

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。

结论

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。

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