首页> 外文会议>2010 IEEE International Ultrasonics Symposium >Enhancement of radiation therapy by ultrasonically-stimulated microbubbles in vitro: Effects of treatment scheduling on cell viability and production of ceramide
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Enhancement of radiation therapy by ultrasonically-stimulated microbubbles in vitro: Effects of treatment scheduling on cell viability and production of ceramide

机译:体外超声刺激的微泡增强放射治疗:治疗计划对细胞活力和神经酰胺产生的影响

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Microbubbles are used as therapeutic agents to improve drug delivery across blood vessels and cell membranes. Recently, it was shown that the application of ultrasound and microbubbles can enhance the therapeutic effect of radiotherapy using in vitro and in vivo tumour models. This phenomenon depended on ultrasound, microbubble and x-ray exposure parameters. In this study, the effect of ultrasound-microbubble (US+MB) and ionizing radiation (XRT) treatment scheduling on cell viability and production of ceramide, an apoptosis messenger, was investigated in vitro. Human prostate cancer (PC3) and KHT-C murine fibrosarcoma cells in suspension were exposed to US+MB (f=500kHz; Pneg=580kPa; PD=32μs; PRF=3kHz; insonation time 30s; and 1% v/v microbubbles (DA04, Artenga Inc.)) and XRT (3 Gy single fraction). Timing between the treatments — immediately (i.e. within 15 minutes), 3 and 6 hours — and their order were varied. Following treatment, cell viability was assessed using clonogenic assay. Ceramide level within cells was quantified for up to 7.5 hours following treatment using immunohistochemistry and spectrophotometry. Ultrasound and microbubbles improved the therapeutic effect of radiotherapy in KHT-C and PC3 cells; cell death increased by ∼3–5 folds with the combined treatment compared to each treatment alone. Maximal KHT-C cell death (70±2%) was achieved when US+MB was followed in three hours by XRT. KHT-C cell death of 43±2% and 25±2% was achieved with US+MB and XRT treatments, respectively. The maximal PC3 cell death (83±2%) was achieved when US+MB was followed by XRT immediately (i.e. within 15 minutes). PC3 cell death of 15±4% and 48±5% was achieved with US+MB and XRT treatments, respectively. US+MB and XRT treatments increased the level of ceramide in both cell lines compared to untreated co--ntrols. A correlation was found between cell death and ceramide at 3 h following treatment for the KHT-C and PC3 cells with correlation coefficients of 0.938 and 0.706, respectively. Ultrasonically-stimulated microbubbles can enhance the therapeutic effect of radiotherapy and the timing between the treatments and their order are important in the optimization of the therapeutic effect of radiotherapy. Future work will investigate this in vivo.
机译:微泡被用作治疗剂,以改善跨血管和细胞膜的药物输送。近来,已经显示出超声和微泡的应用可以增强使用体外和体内肿瘤模型的放射疗法的治疗效果。这种现象取决于超声,微泡和X射线曝光参数。在这项研究中,在体外研究了超声微泡(US + MB)和电离辐射(XRT)处理计划对细胞活力和神经酰胺(一种凋亡信使)的产生的影响。将悬浮液中的人类前列腺癌(PC3)和KHT-C鼠纤维肉瘤细胞暴露于US + MB(f = 500kHz; Pneg = 580kPa; PD =32μs; PRF = 3kHz;声波时间30s;和1%v / v微泡( DA04,Artenga Inc.))和XRT(3 Gy单组分)。两次治疗之间的时间安排(即立即(即15分钟内),3个小时和6个小时之间)以及其顺序有所不同。处理后,使用克隆形成测定法评估细胞生存力。使用免疫组织化学和分光光度法处理后,在长达7.5小时的时间内对细胞内的神经酰胺水平进行定量。超声和微泡改善了放疗对KHT-C和PC3细胞的治疗效果;与单独的每种治疗相比,联合治疗的细胞死亡增加了约3-5倍。 X射线追踪US + MB在三小时后达到了最大的KHT-C细胞死亡(70±2%)。 US + MB和XRT处理分别使KHT-C细胞死亡达到43±2%和25±2%。当US + MB立即进行XRT(即在15分钟之内)时,达到了PC3细胞的最大死亡(83±2%)。 US + MB和XRT处理分别使PC3细胞死亡达到15±4%和48±5%。与未经处理的联合用药相比,US + MB和XRT处理可提高两种细胞系中神经酰胺的水平 -- ntrols。在处理KHT-C和PC3细胞后3小时,发现细胞死亡与神经酰胺之间有相关性,相关系数分别为0.938和0.706。超声刺激的微泡可以增强放射治疗的疗效,而且治疗之间的时间安排和顺序对优化放射治疗的效果很重要。未来的工作将在体内进行研究。

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