Hultström J, Manneberg O, Dopf K, Hertz H M, Brismar H, Wiklund M
Department of Applied Physics, Biomedical and X-Ray Physics, KTH/Albanova, Stockholm, Sweden.
Ultrasound Med Biol. 2007 Jan;33(1):145-51. doi: 10.1016/j.ultrasmedbio.2006.07.024.
Ultrasonic-standing-wave (USW) technology has potential to become a standard method for gentle and contactless cell handling in microfluidic chips. We investigate the viability of adherent cells exposed to USWs by studying the proliferation rate of recultured cells following ultrasonic trapping and aggregation of low cell numbers in a microfluidic chip. The cells form 2-D aggregates inside the chip and the aggregates are held against a continuous flow of cell culture medium perpendicular to the propagation direction of the standing wave. No deviations in the doubling time from expected values (24 to 48 h) were observed for COS-7 cells held in the trap at acoustic pressure amplitudes up to 0.85 MPa and for times ranging between 30 and 75 min. Thus, the results demonstrate the potential of ultrasonic standing waves as a tool for gentle manipulation of low cell numbers in microfluidic systems.
超声驻波(USW)技术有潜力成为微流控芯片中温和且非接触式细胞处理的标准方法。我们通过研究在微流控芯片中对少量细胞进行超声捕获和聚集后再培养细胞的增殖速率,来调查暴露于超声驻波下贴壁细胞的活力。细胞在芯片内形成二维聚集体,并且这些聚集体在垂直于驻波传播方向的细胞培养基连续流作用下保持稳定。对于在声压幅值高达0.85 MPa的陷阱中捕获30至75分钟的COS-7细胞,未观察到其倍增时间与预期值(24至48小时)有偏差。因此,结果证明了超声驻波作为微流控系统中温和操控少量细胞的工具的潜力。