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首页> 外文期刊>Investigative radiology >In Vitro Characterization of Two Different Ultrasmall Iron Oxide Particles for Magnetic Resonance Cell Tracking.
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In Vitro Characterization of Two Different Ultrasmall Iron Oxide Particles for Magnetic Resonance Cell Tracking.

机译:体外表征两种不同的超小氧化铁颗粒,用于磁共振细胞跟踪。

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Fleige G, Seeberger F, Laux D, et al. In vitro characterization of two different ultrasmall iron oxide particles for magnetic resonance cell tracking. Invest Radiol 2002;37:482-488.RATIONALE AND OBJECTIVES Comparison of two different ultrasmall superparamagnetic iron oxide (USPIO) particles in terms of their intracellular cell-labeling properties of macrophages and subsequent visualization by MR imaging.MATERIALS AND METHODS Cultures containing the macrophage cell line P-388D1 were incubated with a neutral carboxydextran-coated USPIO preparation (DDM 43/34/103) or an acidic citrate-coated USPIO (VSOP-C125). Experiments were performed in which incubation concentration and duration were varied and phagocytosis and pinocytosis suppressed by specific inhibitors. In cell culture specimens iron content was measured quantitatively and signal intensities determined by in vitro MR imaging.RESULTS VSOP-C125 is incorporated by cells much faster than DDM 43/34/103 and produces significantly higher final intracellular iron concentrations per cell (3420 vs. 727 ng/million cells). Both preparations show similar signal-reducing effects at MR imaging relative to the Fe content per cell. Intracellular USPIO has a much lower detection threshold at MR imaging (50/80 &mgr;mol/L) than extracellular USPIO in free solution (300 &mgr;mol/L).CONCLUSIONS Citrate-coated USPIO particles VSOP-C125 appear to have more favorable properties for magnetic labeling of macrophages than the carboxydextran-coated USPIO preparation DDM 43/34/103.
机译:Fleige G,Seeberger F,Laux D等。用于磁共振细胞跟踪的两种不同超细氧化铁微粒的体外表征。 Invest Radiol 2002; 37:482-488。理据和目的比较两种不同的超小型超顺磁性氧化铁(USPIO)颗粒在巨噬细胞的细胞内细胞标记特性以及随后通过MR成像的可视化。材料与方法含有巨噬细胞的培养物将细胞系P-388D1与中性羧基葡聚糖包被的USPIO制剂(DDM 43/34/103)或酸性柠檬酸盐包被的USPIO(VSOP-C125)一起孵育。进行了实验,其中改变了孵育浓度和持续时间,并通过特异性抑制剂抑制了吞噬作用和胞饮作用。在细胞培养标本中定量测定铁含量并通过体外MR成像确定信号强度。结果VSOP-C125被细胞掺入的速度比DDM 43/34/103快得多,并且每个细胞产生的最终细胞内铁浓度明显更高(3420 vs. 727 ng /百万个细胞)。相对于每个细胞中的铁含量,两种制剂在MR成像中均显示出相似的信号减少效果。细胞内USPIO在MR成像时的检测阈值(50/80μmol/ L)比细胞外USPIO在游离溶液中的检测阈值(300μmol/ L)低得多。结论柠檬酸盐包覆的USPIO颗粒VSOP-C125似乎更有利巨噬细胞的磁性标记的性能优于羧基葡聚糖包被的USPIO制剂DDM 43/34/103。

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