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使用超短回波时间径向成像和经气管内给予 Gd-DOTA 为基础的纳米粒子进行小鼠的对比增强肺部 MRI。

Contrast enhanced lung MRI in mice using ultra-short echo time radial imaging and intratracheally administrated Gd-DOTA-based nanoparticles.

机构信息

Centre de Recherche Cardio-Thoracique de Bordeaux, U1045, Université Bordeaux Segalen, Bordeaux, France.

出版信息

Magn Reson Med. 2013 Nov;70(5):1419-26. doi: 10.1002/mrm.24580. Epub 2012 Dec 11.

Abstract

PURPOSE

To investigate the in vivo T1 -enhancement of the lung parenchyma in free-breathing healthy mice following intratracheal administration of Gd-DOTA-based nanoparticles, to assess the enhancement kinetics of the instilled contrast medium and to identify its elimination pathways.

METHODS

Ultrashort Echo Time (276 μs) proton MRI of the lung was performed (N = 14) at 4.7 T after the intratracheal instillation of 50 μL of seven different concentrations of contrast agent solution (from 2 to 100 mM of Gd(3+) ). The signal enhancement (SE) in lungs, blood, liver, kidneys, and bladder was assessed (N = 3) for a 50 mM concentration solution at different time points.

RESULTS

The largest SE in lungs (266 ± 14%) was observed for a 50 mM solution of Gd(3+) . In lungs, the SE was observed to decay exponentially with a time constant of 149 ± 51 min. The passage of the nanoparticles from lung tissue to blood and kidneys, and ultimately to the bladder, was observed. No significant hepatic enhancement was measured.

CONCLUSION

This study demonstrates the feasibility of large SEs of lung tissue using intratracheally administrated solutions of Gd-based contrast agents. In future applications, the SE in lungs could be used to image the biodistribution of coadministrated drug aerosols or to selectively enhance lung diseased tissues.

摘要

目的

在自由呼吸的健康小鼠中,通过气管内给药研究基于 Gd-DOTA 的纳米颗粒对肺实质的体内 T1 增强作用,评估注入对比剂的增强动力学,并确定其消除途径。

方法

在 4.7 T 下对肺部进行超短回波时间(276 μs)质子 MRI(N = 14),在气管内滴注 50 μL 的七种不同浓度的对比剂溶液(Gd(3+) 浓度从 2 到 100 mM)后进行。在不同时间点对 50 mM 浓度溶液的肺部、血液、肝脏、肾脏和膀胱的信号增强(SE)进行评估(N = 3)。

结果

观察到 Gd(3+) 浓度为 50 mM 的溶液对肺部的 SE 最大(266 ± 14%)。在肺部,SE 呈指数衰减,时间常数为 149 ± 51 min。观察到纳米颗粒从肺组织转移到血液和肾脏,最终转移到膀胱。未测量到明显的肝增强。

结论

本研究证明了使用气管内给予的基于 Gd 的造影剂溶液可实现肺部的大 SE。在未来的应用中,肺部的 SE 可用于成像联合给予的药物气溶胶的生物分布,或选择性增强肺部患病组织。

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