Department of Bioengineering, University of California at San Diego, La Jolla, CA 92093, USA.
Biomed Microdevices. 2009 Dec;11(6):1223-31. doi: 10.1007/s10544-009-9341-5.
We demonstrate a low-power (<0.1 mW), low-voltage (<10 V(p-p)) on-chip piezoelectrically actuated micro-sorter that can deflect single particles and cells at high-speed. With rhodamine in the stream, switching of flow between channels can be visualized at high actuation frequency (micro1.7 kHz). The magnitude of the cell deflection can be precisely controlled by the magnitude and waveform of input voltage. Both simulation and experimental results indicate that the drag force imposed on the suspended particle/cell by the instantaneous fluid displacement can alter the trajectory of the particle/cell of any size, shape, and density of interest in a controlled manner. The open-loop E. Coli cell deflection experiment demonstrates that the sorting mechanism can produce a throughput of at least 330 cells/s, with a promise of a significantly higher throughput for an optimized design. To achieve close-loop sorting operation, fluorescence detection, real-time signal processing, and field-programmable-gate-array (FPGA) implementation of the control algorithms were developed to perform automated sorting of fluorescent beads. The preliminary results show error-free sorting at a sorting efficiency of micro 70%. Since the piezoelectric actuator has an intrinsic response time of 0.1-1 ms and the sorting can be performed under high flowrate (particle speed of micro 1-10 cm/s), the system can achieve a throughput of >1,000 particles/s with high purity.
我们展示了一种低功率(<0.1mW)、低电压(<10Vpp)的片上压电驱动微分选器,它可以高速偏转单个粒子和细胞。在流中加入罗丹明,可以在高激励频率(微 1.7kHz)下观察到流道之间的切换。通过输入电压的幅度和波形,可以精确控制细胞的偏转幅度。模拟和实验结果都表明,悬浮粒子/细胞所受的流体瞬时位移产生的阻力可以以可控的方式改变任何大小、形状和密度的粒子/细胞的轨迹。对大肠杆菌细胞的开环偏转实验表明,该分选机制的通量至少为 330 个细胞/s,通过优化设计有望实现更高的通量。为了实现闭环分选操作,我们开发了荧光检测、实时信号处理和现场可编程门阵列(FPGA)控制算法的实现,以实现荧光珠的自动分选。初步结果表明,在分选效率为微 70%的情况下,分选无错误。由于压电执行器的固有响应时间为 0.1-1ms,并且可以在高流速下(粒子速度为微 1-10cm/s)进行分选,因此该系统可以实现>1000 个/s 的高纯度吞吐量。