IEEE Trans Ultrason Ferroelectr Freq Control. 2014 Feb;61(2):251-65. doi: 10.1109/TUFFC.2014.6722611.
Histotripsy produces tissue fractionation through dense energetic bubble clouds generated by short, high-pressure, ultrasound pulses. Conventional histotripsy treatments have used longer pulses from 3 to 10 cycles, wherein the lesion-producing bubble cloud generation depends on the pressure-release scattering of very high peak positive shock fronts from previously initiated, sparsely distributed bubbles (the shock-scattering mechanism). In our recent work, the peak negative pressure (P-) for generation of dense bubble clouds directly by a single negative half cycle, the intrinsic threshold, was measured. In this paper, the dense bubble clouds and resulting lesions (in red blood cell phantoms and canine tissues) generated by these supra-intrinsic threshold pulses were studied. A 32-element, PZT-8, 500-kHz therapy transducer was used to generate very short (<2 cycles) histotripsy pulses at a pulse repetition frequency (PRF) of 1 Hz and P- from 24.5 to 80.7 MPa. The results showed that the spatial extent of the histotripsy-induced lesions increased as the applied P- increased, and the sizes of these lesions corresponded well to the estimates of the focal regions above the intrinsic cavitation threshold, at least in the lower pressure regime (P- = 26 to 35 MPa). The average sizes for the smallest reproducible lesions were approximately 0.9 × 1.7 mm (lateral × axial), significantly smaller than the -6-dB beamwidth of the transducer (1.8 × 4.0 mm). These results suggest that, using the intrinsic threshold mechanism, well-confined and microscopic lesions can be precisely generated and their spatial extent can be estimated based on the fraction of the focal region exceeding the intrinsic cavitation threshold. Because the supra-threshold portion of the negative half cycle can be precisely controlled, lesions considerably less than a wavelength are easily produced, hence the term microtripsy.
超声空化爆破通过短而高压的超声脉冲产生密集的高能气泡云,从而实现组织的分割。传统的超声空化爆破治疗使用 3 到 10 个周期的长脉冲,在此期间,产生病变的气泡云的生成取决于先前启动的稀疏分布气泡的高压正冲击波的压力释放散射(冲击波散射机制)。在我们最近的工作中,测量了通过单个负半周期直接产生密集气泡云的峰值负压(P-),即固有阈值。在本文中,研究了这些超阈值脉冲产生的密集气泡云和由此产生的病变(在红细胞模拟物和犬组织中)。使用 32 个元件的 PZT-8、500kHz 治疗换能器以 1Hz 的脉冲重复频率(PRF)和 24.5 至 80.7MPa 的 P-产生非常短的(<2 个周期)超声空化爆破脉冲。结果表明,随着施加的 P-的增加,超声空化爆破诱导的病变的空间范围增大,并且这些病变的尺寸与固有空化阈值以上的焦点区域的估计值非常吻合,至少在较低的压力范围内(P-=26 至 35MPa)。最小可重复病变的平均尺寸约为 0.9×1.7mm(横向×轴向),明显小于换能器的-6dB 束宽(1.8×4.0mm)。这些结果表明,使用固有阈值机制,可以精确地产生良好限定的微观病变,并且可以根据超过固有空化阈值的焦点区域的分数来估计其空间范围。由于可以精确地控制负半周期的超阈值部分,因此很容易产生小于一个波长的病变,因此术语为微爆破。