Institute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, United Kingdom.
Institute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, United Kingdom.
Ultrasound Med Biol. 2020 May;46(5):1235-1243. doi: 10.1016/j.ultrasmedbio.2020.01.009. Epub 2020 Feb 25.
Many useful therapeutic bio-effects can be generated using ultrasound-induced cavitation. However, cavitation is also capable of causing unwanted cellular and vascular damage, which should be monitored to ensure treatment safety. In this work, the unique opportunity provided by passive acoustic mapping (PAM) to quantify cavitation dose across an entire volume of interest during therapy is utilised to provide setup-independent measures of spatially localised cavitation dose. This spatiotemporally quantifiable cavitation dose is then related to the level of cellular damage generated. The cavitation-mediated destruction of equine red blood cells mixed with one of two types of cavitation nuclei at a variety of concentrations is investigated. The blood is placed within a 0.5-MHz ultrasound field and exposed to a range of peak rarefactional pressures up to 2 MPa, with 50 to 50,000 cycle pulses maintaining a 5% duty cycle. Two co-planar linear arrays at 90° to each other are used to generate 400-µm-resolution frequency domain robust capon beamforming PAM maps, which are then used to generate estimates of cavitation dose. A relationship between this cavitation dose and the levels of haemolysis generated was found which was comparable regardless of the applied acoustic pressure, pulse length, cavitation agent type or concentration used. PAM was then used to monitor cellular damage in multiple locations within a tissue phantom simultaneously, with the damage-cavitation dose relationship being similar for the two experimental models tested. These results lay the groundwork for this method to be applied to other measures of safety, allowing for improved ultrasound monitoring of cavitation-based therapies.
利用超声空化可以产生许多有用的治疗生物效应。然而,空化也有能力造成不必要的细胞和血管损伤,因此应该进行监测以确保治疗安全。在这项工作中,利用被动声映射(PAM)在治疗过程中对整个感兴趣体积内的空化剂量进行量化的独特机会,提供了与空间局部空化剂量相关的独立于设置的测量方法。然后将这种时空可量化的空化剂量与产生的细胞损伤水平相关联。研究了在各种浓度下,与两种类型的空化核混合的马的红细胞在 0.5MHz 超声场中的空化介导破坏。将血液置于高达 2MPa 的峰值稀疏压力范围内的一系列峰值稀疏压力下,使用 50 至 50,000 个循环脉冲,保持 5%的占空比。两个相互成 90°的共面线性阵列用于生成具有 400-µm 分辨率的频域鲁棒 Capon 波束形成 PAM 图,然后使用这些图生成空化剂量的估计值。发现这种空化剂量与产生的溶血水平之间存在关系,无论施加的声压、脉冲长度、空化剂类型或浓度如何,这种关系都是相似的。然后,PAM 用于同时监测组织模型内多个位置的细胞损伤,两种实验模型的损伤-空化剂量关系相似。这些结果为该方法应用于其他安全措施奠定了基础,允许对基于空化的治疗进行更有效的超声监测。