a Physical Sciences Platform , Sunnybrook Research Institute , Toronto , Canada.
b Department of Medical Biophysics , University of Toronto , Toronto , Canada.
Int J Hyperthermia. 2018;35(1):599-611. doi: 10.1080/02656736.2018.1514468. Epub 2018 Oct 8.
Ultrasound contrast agent microbubbles were combined with magnetic resonance imaging (MRI)-guided focused ultrasound (MRgFUS) as a means to achieve mild hyperthermia at reduced power levels.
MRgFUS hyperthermia (42°C for 20 min) was evaluated in rabbit thigh muscle or Vx2 tumors using infusions of microbubbles (Definity, 20 µL/kg) or saline (sham) administered over 5 min. The impact of treatments on drug uptake was assessed with liposomal doxorubicin (Caelyx, 2.5 mg/kg). Applied power levels before and after the injection of microbubbles or saline were compared, and drug uptake was evaluated with fluorometry of tissues harvested 24 hr post-treatment.
MRgFUS hyperthermia in muscle and tumors resulted in accurate temperature control (mean =42.0°C, root mean square error (RMSE) = 0.3°C). The power dropped significantly following the injection of microbubbles in muscle and tumors compared to exposures without microbubbles (-21.9% ± 12.5% vs -5.9% ± 7.8%, p = .009 in muscle; -33.8% ± 9.9% vs -3.0% ± 7.2%, p < .001 in tumors). Cavitation monitoring indicated emission of subharmonic, ultraharmonic, and elevated levels of fourth to sixth harmonic frequencies following microbubble injection. The drug delivery was elevated significantly in muscle with the use of microbubble-assisted relative to conventional heating (0.5 ± 0.5 ng/mg vs 0.20 ± 0.04 ng/mg, p = .05), whereas in tumors similar levels were found (11 ± 3 ng/mg vs 16 ± 4 ng/mg, p = .13).
The finding that microbubbles reduce the applied power requirements for hyperthermia has considerable clinical implications. The elevated levels of drug found in muscle but not tumor tissue suggest a complex interplay between the heating effects of microbubbles with those of enhanced permeabilization and possible vascular damage.
超声造影微泡与磁共振引导聚焦超声(MRgFUS)联合应用,以在较低功率水平下实现温和的热疗。
使用兔大腿肌肉或 Vx2 肿瘤,通过微泡(Definity,20 μL/kg)或生理盐水(假处理)输注 5 分钟,评估 MRgFUS 热疗(42°C 20 分钟)。使用脂质体阿霉素(Caelyx,2.5mg/kg)评估处理对药物摄取的影响。比较微泡或生理盐水注射前后的应用功率水平,并通过治疗后 24 小时采集的组织荧光光度法评估药物摄取。
肌肉和肿瘤中的 MRgFUS 热疗可实现精确的温度控制(平均值=42.0°C,均方根误差(RMSE)=0.3°C)。与无微泡暴露相比,肌肉和肿瘤中的微泡注射后功率显著下降(-21.9%±12.5%比-5.9%±7.8%,p=0.009;-33.8%±9.9%比-3.0%±7.2%,p<0.001)。空化监测表明,微泡注射后会发射亚谐波、超谐波和第四到第六次谐波的升高频率。与常规加热相比,肌肉中使用微泡辅助的药物输送显著升高(0.5±0.5ng/mg 比 0.20±0.04ng/mg,p=0.05),而在肿瘤中则发现类似水平(11±3ng/mg 比 16±4ng/mg,p=0.13)。
发现微泡降低了热疗的应用功率要求,这具有重要的临床意义。在肌肉中发现的升高水平的药物,但在肿瘤组织中没有发现,这表明微泡的加热效应与增强的通透性和可能的血管损伤之间存在复杂的相互作用。