首页> 外文会议>Ultrasonics Symposium (IUS), 2008 IEEE >Delivery of fluorescent dextrans through the ultrasound-induced blood-brain barrier opening in mice
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Delivery of fluorescent dextrans through the ultrasound-induced blood-brain barrier opening in mice

机译:通过超声诱导的小鼠血脑屏障开放传递荧光葡聚糖

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The blood-brain barrier (BBB) is a specialized brain protection system consisting of endothelial cell, tight junctions and glial processes. BBB is the major limiting factor to delivering therapeutic agents to the brain for disease treatment. Focused ultrasound (FUS) in the presence of microbubbles has the capability to deliver large molecules across BBB. In this study, we qualitatively and quantitatively analyzed the cellular impact, the size estimation of the opening and the amount delivered into the brain parenchyma in murine model. The method involved intravenously administration of a bolus of microbubbles at 1 μl/g body weight. Pulsed FUS was applied to the left hippocampus through the intact skin and skull at 0.75 MPa peak-negative pressure followed by a separate intravenously administration of fluorescence-conjugated dextrans at 3 kDa, 10 kDa and 70 kDa. Qualitative analysis was evaluated through the fluorescence imaging of sectioned brain slices. Smooth muscle cells engulfing the capillaries exhibited higher fluorescence in the case of 70 kDa dextran once the BBB was opened. The dextran dose delivered into the brain was analyzed by brain tissue homogenization and fluorescence intensity measurement. The concentration of 3 kDa, 10 kDa and 70 kDa dextrans delivered to the left hemisphere was quantified to be equal to 7.9±4.9 μg/g, 2.4±1.3 μg/g and 0.9± 0.47μg/g of brain weight. In conclusion, significant drug delivery and the net deposition to the sonicated hippocampus, compared to the non-sonicated hippocampus, were determined. The delivered dosage and the spatial distribution provide useful information for the ultimate treatment of neurodegenerative diseases.
机译:血脑屏障(BBB)是一种专门的大脑保护系统,由内皮细胞,紧密连接和神经胶质过程组成。 BBB是将治疗剂输送到大脑进行疾病治疗的主要限制因素。存在微气泡的聚焦超声(FUS)具有将大分子穿过BBB输送的能力。在这项研究中,我们定性和定量地分析了小鼠模型中细胞的影响,开口的大小估计以及传递到脑实质中的数量。该方法涉及以1μl/ g体重静脉内施用一团微泡。在0.75 MPa峰值负压下,通过完整的皮肤和颅骨向左海马施加脉冲FUS,然后分别静脉内施用3 kDa,10 kDa和70 kDa的荧光偶联右旋糖酐。通过切片的脑切片的荧光成像评估定性分析。一旦打开BBB,吞噬毛细血管的平滑肌细胞在70 kDa葡聚糖的情况下会显示更高的荧光。通过脑组织均质化和荧光强度测量来分析递送至大脑的右旋糖酐剂量。传递到左半球的3 kDa,10 kDa和70 kDa右旋糖酐的浓度被量化为等于脑重量的7.9±4.9μg/ g,2.4±1.3μg/ g和0.9±0.47μg/ g。总之,与未超声处理的海马相比,确定了超声处理海马的显着药物递送和净沉积。递送的剂量和空间分布为神经退行性疾病的最终治疗提供了有用的信息。

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