Siu Tung, Rohling Robert N, Chiao Mu
Department of Mechanical Engineering, University of British Columbia, 6250 Applied Science Lane, UBC, Vancouver, BC, V6T 1ZT, Canada.
Biomed Microdevices. 2008 Feb;10(1):89-97. doi: 10.1007/s10544-007-9113-z.
In this paper, we propose the use of micro-ultrasonic transducers (MUTs) for a therapeutic application in combination with a cancer drug. In particular, sonodynamic enhancement of doxorubicin cytotoxicity was investigated in vitro using human prostate cancer cells (PC3). Cells in suspensions were found to be two to three times more prone to the cytotoxic effect of ultrasound than adherent cells. With 60 s of tone-burst ultrasound (4 MHz, 50 ms repetition period, and 25% duty cycle) at 40 Watt/cm(2) (spatial average-temporal average), cytotoxicity of doxorubicin treatment of adherent cells increased from 27 to 91%. The threshold ultrasonic power density required for any cytotoxicity enhancement to be observable was found to be 15 Watt/cm(2) for PC3 cells with doxorubicin and tone burst ultrasound at 4 MHz. This is a level achievable by MUTs. The long term vision is to design implantable MUTs for sonodynamic therapy with the goal of improving treatment efficacy.
在本文中,我们提出将微超声换能器(MUTs)用于与抗癌药物联合的治疗应用。特别地,使用人前列腺癌细胞(PC3)在体外研究了阿霉素细胞毒性的声动力增强。发现悬浮液中的细胞比贴壁细胞对超声细胞毒性作用的敏感性高两到三倍。在40瓦/平方厘米(空间平均-时间平均)下进行60秒的脉冲超声(4兆赫,50毫秒重复周期,25%占空比),阿霉素处理贴壁细胞的细胞毒性从27%增加到91%。对于PC3细胞,在4兆赫下使用阿霉素和脉冲超声时,可观察到任何细胞毒性增强所需的阈值超声功率密度为15瓦/平方厘米。这是MUTs能够达到的水平。长期目标是设计用于声动力治疗的可植入MUTs,以提高治疗效果。