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Monitoring of focused ultrasound-induced blood-brain barrier opening in non-human primates using transcranial cavitation detection in vivo and the primate skull effect

机译:使用体内经颅空化检测和灵长类动物头骨效应监测超声聚焦在非人灵长类动物中引起的血脑屏障开放

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Focused ultrasound (FUS) with microbubbles (MB) is promising for assisting the delivery of drugs across the blood-brain barrier (BBB). To assess the safety and efficacy, the monitoring using passive cavitation detection (PCD) is critical and yet the reliability of transcranial detection in large animals remained questioned. To study the primate skull effect, the PCD through the in-vitro monkey and human skulls and in the in vivo monkeys during the sonication (FUS frequency: 500 kHz) were investigated, with the use of in-house made lipid-shelled, monodisperse MB (median diameter: 4-5 μm) and a flatband hydrophone served as a passive cavitation detector. In the in vitro experiments, the MB were injected to the channel of the phantom under a degassed skull for sonication (peak negative pressure/PNP: 50-450 kPa, pulse length/PL: 0.2 ms, PRF: 10 Hz, duration: 2 s). A diagnostic B-mode imaging system was also used to monitor the cavitation. In the in vivo study, the PCD was realtime monitored during the sonication for PCD calibration (PNP: 50-700 kPa, PL: 0.2 ms and 10 ms, PRF: 2 Hz, duration: 10 s) and BBB opening (PNP: 200-600 kPa, PL: 10 ms, PRF: 2 Hz, duration: 2 min). The stable cavitation dose using harmonics (SCDh) and ultraharmonics (SCDu) and the inertial cavitation dose (ICD) were quantified. Results showed that the SCDh, SCDu, and ICD were detectable in vitro at 50 kPa and above, and the B-mode imaging showed bubble collapse at 200 kPa and above. The detection thresholds increased with the skulls in place, with the signal reduction of 15.4 dB for the monkey skull and 34.1 dB for the human skull. In the in vivo experiments, the SCDh and ICD was detectable at and above 100 kPa and 250 kPa, respectively, and the SCDu was less reliable due to spontaneous occurrence. The BBB was found to be disrupted in 250-600 kPa without edema, hemorrhage, and physiological changes were found. In conclusion- the SCDh was more detectable and reliable than the SCDu in assessing stable cavitation in vivo, and the inertial cavitation was detected at 250 kPa and may occur at lower pressures.
机译:具有微泡(MB)的聚焦超声(FUS)有望协助药物穿过血脑屏障(BBB)的输送。为了评估安全性和有效性,使用被动空化检测(PCD)进行监测非常关键,但是在大型动物中经颅检测的可靠性仍然受到质疑。为了研究灵长类动物的颅骨效应,在超声处理(FUS频率:500 kHz)期间,研究了通过体外猴子和人类头骨以及体内猴子的PCD,并使用了自制的脂质壳单分散体MB(中值直径:4-5μm)和一个平板水听器用作被动气蚀检测器。在体外实验中,将MB注射到脱气的颅骨下的体模通道中进行超声处理(峰值负压/ PNP:50-450 kPa,脉冲长度/ PL:0.2 ms,PRF:10 Hz,持续时间:2 s)。诊断性B型成像系统也用于监测气蚀现象。在体内研究中,在超声处理过程中对PCD进行了实时监控,以进行PCD校准(PNP:50-700 kPa,PL:0.2 ms和10 ms,PRF:2 Hz,持续时间:10 s)和BBB开放(PNP:200) -600 kPa,PL:10毫秒,PRF:2 Hz,持续时间:2分钟)。定量了使用谐波(SCD h )和超谐波(SCD u )的稳定空化剂量和惯性空化剂量(ICD)。结果表明,在50 kPa及以上的体外可检测到SCD h ,SCD u 和ICD,而B型成像显示在200 kPa及以上时气泡破裂。检测阈值随头骨的位置而增加,猴头骨和人头骨的信号降低分别为15.4 dB和34.1 dB。在体内实验中,SCD h 和ICD分别在100 kPa和250 kPa及以上时可检测到,并且SCD u 由于自发性而较不可靠。发现BBB在250-600 kPa时破裂,没有水肿,出血和生理变化。结论:在评估体内稳定的空化方面,SCD h 比SCD u 更可检测且更可靠,并且在250 kPa处可检测到惯性空化,并且可能在较低的情况下发生压力。

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