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Permeability dependence study of the focused ultrasound-induced blood–brain barrier opening at distinct pressures and microbubble diameters using DCE-MRI

机译:使用DCE-MRI对超声在不同压力和微气泡直径下聚焦的血脑屏障开放的渗透性依赖性研究

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Blood–brain barrier opening using focused ultrasound and microbubbles has been experimentally established as a noninvasive and localized brain drug delivery technique. In this study, the permeability of the opening is assessed in the murine hippocampus after the application of focused ultrasound at three different acoustic pressures and microbubble sizes. Using dynamic contrast-enhanced MRI, the transfer rates were estimated, yielding permeability maps and quantitative Ktrans values for a predefined region of interest. The volume of blood–brain barrier opening according to the Ktrans maps was proportional to both the pressure and the microbubble diameter. A Ktrans plateau of ∼0.05 min−1 was reached at higher pressures (0.45 and 0.60 MPa) for the larger sized bubbles (4–5 and 6–8 μm), which was on the same order as the Ktrans of the epicranial muscle (no barrier). Smaller bubbles (1–2 μm) yielded significantly lower permeability values. A small percentage (7.5%) of mice showed signs of damage under histological examination, but no correlation with permeability was established. The assessment of the blood–brain barrier permeability properties and their dependence on both the pressure and the microbubble diameter suggests that Ktrans maps may constitute an in vivo tool for the quantification of the efficacy of the focused ultrasound-induced blood–brain barrier opening. Magn Reson Med, 2011. © 2011 Wiley-Liss, Inc.
机译:通过聚焦超声和微泡打开血脑屏障已被实验确定为一种非侵入性的局部脑部药物递送技术。在这项研究中,在三种不同的声压和微气泡尺寸下应用聚焦超声后,在鼠海马中评估开口的通透性。使用动态对比度增强的MRI,可以估算传输速率,得出通透性图和预定的感兴趣区域的定量K trans 值。根据K trans 图的血脑屏障开放量与压力和微泡直径成正比。对于较大尺寸的气泡(4–5和6–8μm),在较高压力(0.45和0.60 MPa)下达到了AK trans 平台,约为0.05 min -1 ,其顺序与epi上肌的K trans 相同(无障碍)。较小的气泡(1-2μm)产生较低的渗透率值。少量(7.5%)的小鼠在组织学检查中显示有损伤迹象,但与通透性没有相关性。对血脑屏障通透性特性及其对压力和微气泡直径的依赖性的评估表明,K trans 图可能构成体内工具,用于量化聚焦超声的功效,导致血脑屏障开放。 Magn Reson Med,2011年。©2011 Wiley-Liss,Inc.。

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