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利用超声和微泡暂时破坏血脑屏障:恒河猴的安全性和有效性评估。

Temporary disruption of the blood-brain barrier by use of ultrasound and microbubbles: safety and efficacy evaluation in rhesus macaques.

机构信息

Department of Radiology, Brigham & Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Cancer Res. 2012 Jul 15;72(14):3652-63. doi: 10.1158/0008-5472.CAN-12-0128. Epub 2012 May 2.

Abstract

The blood-brain barrier (BBB) prevents entry of most drugs into the brain and is a major hurdle to the use of drugs for brain tumors and other central nervous system disorders. Work in small animals has shown that ultrasound combined with an intravenously circulating microbubble agent can temporarily permeabilize the BBB. Here, we evaluated whether this targeted drug delivery method can be applied safely, reliably, and in a controlled manner on rhesus macaques using a focused ultrasound system. We identified a clear safety window during which BBB disruption could be produced without evident tissue damage, and the acoustic pressure amplitude where the probability for BBB disruption was 50% and was found to be half of the value that would produce tissue damage. Acoustic emission measurements seem promising for predicting BBB disruption and damage. In addition, we conducted repeated BBB disruption to central visual field targets over several weeks in animals trained to conduct complex visual acuity tasks. All animals recovered from each session without behavioral deficits, visual deficits, or loss in visual acuity. Together, our findings show that BBB disruption can be reliably and repeatedly produced without evident histologic or functional damage in a clinically relevant animal model using a clinical device. These results therefore support clinical testing of this noninvasive-targeted drug delivery method.

摘要

血脑屏障(BBB)阻止了大多数药物进入大脑,这是将药物用于脑肿瘤和其他中枢神经系统疾病的主要障碍。在小动物中的研究表明,超声联合静脉循环微泡剂可以暂时使 BBB 通透性增加。在这里,我们使用聚焦超声系统评估了这种靶向药物递送方法是否可以在恒河猴中安全、可靠和可控地应用。我们确定了一个明确的安全窗口,在此期间可以在没有明显组织损伤的情况下产生 BBB 破坏,并且发现 BBB 破坏的概率为 50%的声压幅度是会产生组织损伤的声压幅度的一半。声发射测量似乎有望用于预测 BBB 破坏和损伤。此外,我们在经过训练以进行复杂视力任务的动物中,对中央视野目标进行了多次 BBB 破坏,持续数周。每次治疗后,所有动物均未出现行为缺陷、视觉缺陷或视力下降而恢复。总之,我们的研究结果表明,在使用临床设备的临床相关动物模型中,可以可靠且反复地产生 BBB 破坏,而不会出现明显的组织学或功能损伤。因此,这些结果支持对这种非侵入性靶向药物递送方法进行临床测试。

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