Hsu Yu-Hone, Lee Wei-Chung, Chu Shing-Shung, Chao Meng-En, Wu Kuo-Sheng, Liu Ren-Shyan, Wong Tai-Tong
Division of Neurosurgery, Kaohsiung Veterans General Hospital, Zuoying, Kaohsiung 813, Taiwan.
School of Nursing, National Taipei University of Nursing and Health Sciences, Taipei 112, Taiwan.
Pharmaceutics. 2022 Jun 6;14(6):1207. doi: 10.3390/pharmaceutics14061207.
Pulsed ultrasound combined with microbubbles use can disrupt the blood-brain barrier (BBB) temporarily; this technique opens a temporal window to deliver large therapeutic molecules into brain tissue. There are published studies to discuss the efficacy and safety of the different ultrasound parameters, microbubble dosages and sizes, and sonication schemes on BBB disruption, but optimal the paradigm is still under investigation. Our study is aimed to investigate how different sonication parameters, time, and microbubble dose can affect BBB disruption, the dynamics of BBB disruption, and the efficacy of different sonication schemes on BBB disruption. We used pulsed weakly focused ultrasound to open the BBB of C57/B6 mice. Evans blue dye (EBD) was used to determine the degree of BBB disruption. With a given acoustic pressure of 0.56 MPa and pulse repetitive frequency of 1 Hz, burst lengths of 10 ms to 50 ms, microbubbles of 100 μL/kg to 300 μL/kg, and sonication times of 60 s to 150 s were used to open the BBB for parameter study. Brain EBD accumulation was measured at 1, 4, and 24 h after sonication for the time-response relationship study; EBD of 100 mg/kg to 200 mg/kg was administered for the dose-response relationship study; EBD injection 0 to 6 h after sonication was performed for the BBB disruption dynamic study; brain EBD accumulation induced by one sonication and two sonications was investigated to study the effectiveness on BBB disruption; and a histology study was performed for brain tissue damage evaluation. Pulsed weakly focused ultrasound opens the BBB extensively. Longer burst lengths and a larger microbubble dose result in a higher degree of BBB disruption; a sonication time longer than 60 s did not increase BBB disruption; brain EBD accumulation peaks 1 h after sonication and remains 81% of the peak level 24 h after sonication; the EBD dose administered correlates with brain EBD accumulation; BBB disruption decreases as time goes on after sonication and lasts for 6 h at least; and brain EBD accumulation induced by two sonication increases 74.8% of that induced by one sonication. There was limited adverse effects associated with sonication, including petechial hemorrhages and mild neuronal degeneration. BBB can be opened extensively and reversibly by pulsed weakly focused ultrasound with limited brain tissue damage. Since EBD combines with albumin in plasma to form a conjugate of 83 kDa, these results may simulate ultrasound-induced brain delivery of therapeutic molecules of this size scale. The result of our study may contribute to finding the optimal paradigm of focused ultrasound-induced BBB disruption.
脉冲超声联合微泡的应用能够暂时破坏血脑屏障(BBB);该技术开启了一个时间窗口,以便将大型治疗性分子递送至脑组织。已有发表的研究讨论了不同超声参数、微泡剂量和大小以及超声处理方案对血脑屏障破坏的有效性和安全性,但最佳模式仍在研究中。我们的研究旨在探究不同的超声处理参数、时间和微泡剂量如何影响血脑屏障破坏、血脑屏障破坏的动力学以及不同超声处理方案对血脑屏障破坏的效果。我们使用脉冲弱聚焦超声打开C57/B6小鼠的血脑屏障。伊文思蓝染料(EBD)用于确定血脑屏障破坏的程度。在给定声压0.56MPa、脉冲重复频率1Hz的情况下,使用10ms至50ms的脉冲长度、100μL/kg至300μL/kg的微泡以及60s至150s的超声处理时间来打开血脑屏障进行参数研究。在超声处理后1小时、4小时和24小时测量脑内EBD蓄积,以进行时间 - 反应关系研究;给予100mg/kg至200mg/kg的EBD进行剂量 - 反应关系研究;在超声处理后0至6小时注射EBD进行血脑屏障破坏动态研究;研究一次超声处理和两次超声处理诱导的脑内EBD蓄积,以研究对血脑屏障破坏的效果;并进行组织学研究以评估脑组织损伤。脉冲弱聚焦超声可广泛打开血脑屏障。更长的脉冲长度和更大的微泡剂量会导致更高程度的血脑屏障破坏;超声处理时间超过60s并不会增加血脑屏障破坏程度;脑内EBD蓄积在超声处理后1小时达到峰值,在超声处理后24小时仍保持峰值水平的81%;给予的EBD剂量与脑内EBD蓄积相关;血脑屏障破坏在超声处理后随时间推移而降低,且至少持续6小时;两次超声处理诱导的脑内EBD蓄积比一次超声处理增加74.8%。超声处理相关的不良反应有限,包括瘀点出血和轻度神经元变性。脉冲弱聚焦超声可广泛且可逆地打开血脑屏障,同时对脑组织损伤有限。由于EBD与血浆中的白蛋白结合形成83kDa的复合物,这些结果可能模拟了超声诱导的该尺寸规模治疗性分子的脑内递送。我们的研究结果可能有助于找到聚焦超声诱导血脑屏障破坏的最佳模式。