Göllner Simon, Colditz Melanie, Huang Yishu, Schmidt Hagen, Winkler Andreas, Stiel Andre C
Institute of Biological and Medical Imaging, Helmholtz Zentrum München, Neuherberg, Bavaria 85764, Germany.
Chair of Biological Imaging, Central Institute for Translational Cancer Research (TranslaTUM), School of Medicine and Health & School of Computation, Information and Technology, Technical University of Munich, Munich 80333, Germany.
ACS Appl Mater Interfaces. 2025 Mar 12;17(10):14903-14911. doi: 10.1021/acsami.4c20182. Epub 2025 Feb 25.
Sensitive measurement of the optoacoustic (OA, also photoacoustic) properties of cells in flow is highly desirable, as it provides information about the optical absorption properties of cellular compounds. Hence, optoacoustic spectral characteristics can deliver information about the cell state or disease parameters, but can also be used for high-throughput cell sorting by intrinsic properties without additional fluorescence labeling. The current implementation of optoacoustic measurements of cells in a microfluidic context typically relies on piezoelectric (ultrasound) transducers attached to the microfluidic chip, whereby the transducer records the ultrasound signal originating from absorbing species in cells when excited by laser pulses. The arrangement of the transducer outside of the microfluidic chip leads to the challenge of signal integration over a larger area and coupling interlayer effects resulting in attenuation and a reduction of sensitivity. Moreover, the placement of the bulky transducer outside of the chip prevents the exploitation of the full advantages of microfluidics. As a solution, we demonstrate the use of point-source optimized interdigital transducers (pIDTs) directly fabricated on the surface of the microfluidic chip for the detection of surface acoustic waves (SAW) from single cells in continuous flow. The SAW is excited by bulk acoustic waves originating from the optoacoustic effect of absorbing species inside the cells illuminated by laser light. The use of these highly focused pIDTs and on-chip lithographically fabricated hard-wall microchannels allows the detection of SAW with a spatial resolution on the order of the cell diameter directly on-chip, offering the possibility of miniaturization, parallelization, and cheap mass production.
对流动中的细胞进行光声(OA,也称为光声)特性的灵敏测量非常必要,因为它能提供有关细胞化合物光学吸收特性的信息。因此,光声光谱特征不仅可以传递有关细胞状态或疾病参数的信息,还可用于基于固有特性的高通量细胞分选,而无需额外的荧光标记。目前在微流控环境下对细胞进行光声测量的方法通常依赖于附着在微流控芯片上的压电(超声)换能器,当被激光脉冲激发时,该换能器记录源自细胞中吸收物质的超声信号。换能器位于微流控芯片外部的这种布置带来了在更大面积上进行信号整合以及层间耦合效应的挑战,从而导致信号衰减和灵敏度降低。此外,体积较大的换能器放置在芯片外部阻碍了对微流控技术全部优势的利用。作为一种解决方案,我们展示了直接在微流控芯片表面制造的点源优化叉指换能器(pIDT)用于检测连续流动中单个细胞产生的表面声波(SAW)。SAW由激光照射的细胞内吸收物质的光声效应产生的体声波激发。使用这些高度聚焦的pIDT以及芯片上光刻制造的硬壁微通道,能够直接在芯片上以细胞直径量级的空间分辨率检测SAW,提供了小型化、并行化和廉价大规模生产的可能性。