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Focused ultrasound-induced blood-brain barrier disruption enhances the delivery of cytarabine to the rat brain

机译:聚焦超声诱导的血脑屏障破坏增强了阿糖胞苷向大鼠脑的传递

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摘要

To investigate the feasibility of using focused ultrasound (FUS) with microbubbles for targeted delivery of cytarabine to the brain. Sprague-Dawly rats (weighing 200-250 g) received focused ultrasound with intravenous injection microbubbles. At 0, 2, 4, 8, and 24 hours (n55 for each time point) after sonication, animals received intravenous administration of cytarabine at a normal dose of 4 mg/kg body weight. Additional five rats were given with a high dose (50 mg/kg body weight) of cytarabine alone. Blood-brain barrier (BBB) permeability and cerebral cytarabine were determined. FUS in conjunction with microbubbles caused a transient BBB opening. Sonication exposure promoted cytarabine accumulation at the sonicated site. Animals injected with a normal dose of cytarabine 2 hours after sonication had similar concentrations of cerebral cytarabine compared to those with higher cytarabine without sonication. FUS can temporarily open the BBB and thus facilitate the penetration of systemic cytarabine into the brain.
机译:为了研究将聚焦超声(FUS)与微泡一起用于将阿糖胞苷定向递送到大脑的可行性。 Sprague-Dawly大鼠(体重200-250 g)接受聚焦超声和静脉注射微泡。在超声处理后的0、2、4、8和24小时(每个时间点n55),动物接受了正常剂量4 mg / kg体重的阿糖胞苷静脉内给药。另外五只大鼠单独给予高剂量(50 mg / kg体重)的阿糖胞苷。测定血脑屏障(BBB)通透性和脑阿糖胞苷。 FUS与微气泡一起导致短暂的BBB开放。超声处理促进了阿糖胞苷在超声处理部位的蓄积。超声处理2小时后注射正常剂量阿糖胞苷的动物与不进行超声处理的阿糖胞苷较高的动物相比,脑阿糖胞苷的浓度相似。 FUS可以暂时打开血脑屏障,从而促进全身性阿糖胞苷渗透到大脑。

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