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通过聚焦超声控制纳米乳剂药物释放实现的无创靶向经颅神经调节。

Noninvasive Targeted Transcranial Neuromodulation via Focused Ultrasound Gated Drug Release from Nanoemulsions.

作者信息

Airan Raag D, Meyer Randall A, Ellens Nicholas P K, Rhodes Kelly R, Farahani Keyvan, Pomper Martin G, Kadam Shilpa D, Green Jordan J

机构信息

Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine , Baltimore, Maryland 21231, United States.

Department of Biomedical Engineering and the Translational Tissue Engineering Center, Johns Hopkins University School of Medicine , Baltimore, Maryland 21231, United States.

出版信息

Nano Lett. 2017 Feb 8;17(2):652-659. doi: 10.1021/acs.nanolett.6b03517. Epub 2017 Jan 23.

Abstract

Targeted, noninvasive neuromodulation of the brain of an otherwise awake subject could revolutionize both basic and clinical neuroscience. Toward this goal, we have developed nanoparticles that allow noninvasive uncaging of a neuromodulatory drug, in this case the small molecule anesthetic propofol, upon the application of focused ultrasound. These nanoparticles are composed of biodegradable and biocompatible constituents and are activated using sonication parameters that are readily achievable by current clinical transcranial focused ultrasound systems. These particles are potent enough that their activation can silence seizures in an acute rat seizure model. Notably, there is no evidence of brain parenchymal damage or blood-brain barrier opening with their use. Further development of these particles promises noninvasive, focal, and image-guided clinical neuromodulation along a variety of pharmacological axes.

摘要

对清醒状态下的受试者大脑进行靶向、非侵入性神经调节,可能会给基础神经科学和临床神经科学带来变革。为实现这一目标,我们研发出了纳米颗粒,在聚焦超声作用下,这些纳米颗粒能够实现对神经调节药物(在本研究中为小分子麻醉剂丙泊酚)的非侵入性解笼激活。这些纳米颗粒由可生物降解且生物相容的成分组成,并使用当前临床经颅聚焦超声系统易于实现的超声处理参数进行激活。这些颗粒的效力足以在急性大鼠癫痫模型中通过激活来抑制癫痫发作。值得注意的是,使用这些颗粒时没有脑实质损伤或血脑屏障开放的迹象。这些颗粒的进一步研发有望沿着多种药理学途径实现非侵入性、局部性和图像引导的临床神经调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7a8/5362146/021acad9ef2b/nl-2016-035174_0001.jpg

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