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首页> 外文期刊>Molecular imaging and biology: MIB : the official publication of the Academy of Molecular Imaging >MRI Tracking of Macrophages Labeled with Glucan Particles Entrapping a Water Insoluble Paramagnetic Gd-Based Agent
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MRI Tracking of Macrophages Labeled with Glucan Particles Entrapping a Water Insoluble Paramagnetic Gd-Based Agent

机译:巨噬细胞标记的葡聚糖颗粒的MRI跟踪捕获了水不溶的顺磁性Gd基试剂

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摘要

Purpose: This study is aimed at demonstrating the in vivo potential of Gd(III)-loaded glucan particles (Gd-GPs) as magnetic resonance imaging (MRI)-positive agents for labeling and tracking phagocytic cells. Procedure: GPs were obtained from Saccharomyces cerevisae and loaded with the water-insoluble complex Gd-DOTAMA(C18)2. The uptake kinetics of Gd-GPs by murine macrophages was studied in vitro and the internalization mechanism was assessed by competition assays. The in vivo performance of Gd-GPs was tested at 7.05 T on a mouse model of acute liver inflammation. Results: The minimum number of Gd-GPs-labeled J774.A1 macrophages detected in vitro by MRI was ca. 300 cells/μl of agar, which is the lowest number ever reported for cells labeled with a positive T1 agent. Intravenous injection of macrophages labeled with Gd-GPs in a mouse model of liver inflammation enabled the MRI visualization of the cellular infiltration in the diseased area. Conclusions: Gd-GPs represent a promising platform for tracking macrophages by MRI as a T1 alternative to the golden standard T2-based iron oxide particles.
机译:目的:这项研究旨在证明在体内装载Gd(III)的葡聚糖颗粒(Gd-GPs)作为磁共振成像(MRI)阳性试剂的潜力,以标记和追踪吞噬细胞。方法:从酿酒酵母中获得GP,并加入水不溶性复合物Gd-DOTAMA(C18)2。体外研究了鼠巨噬细胞对Gd-GPs的吸收动力学,并通过竞争测定法评估了其内在化机理。在7.05 T的急性肝炎小鼠模型上测试了Gd-GP的体内性能。结果:MRI体外检测到的Gd-GPs标记的J774.A1巨噬细胞的最小数目为。 300个细胞/μl琼脂,这是有报道的用T1阳性试剂标记的细胞的最低数量。在肝炎的小鼠模型中静脉注射标有Gd-GP的巨噬细胞,可以对患病区域的细胞浸润进行MRI可视化。结论:Gd-GPs是通过MRI追踪巨噬细胞的有前途的平台,可作为金标准T2基氧化铁粒子的T1替代品。

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