Department of Pharmaceutical Sciences, University of Illinois Chicago, Chicago, Illinois, United States of America.
Department of Biomedical Engineering, University of Illinois Chicago, Chicago, Illinois, United States of America.
PLoS One. 2023 Jan 17;18(1):e0279102. doi: 10.1371/journal.pone.0279102. eCollection 2023.
Hydrodynamic focusing capable of readily producing and controlling laminar flow facilitates drug treatment of cells in existing microfluidic culture devices. However, to expand applications of such devices to multiparameter drug testing, critical limitations in current hydrodynamic focusing microfluidics must be addressed. Here we describe hydrodynamic focusing and shifting as an advanced microfluidics tool for spatially selective drug delivery and integrative cell-based drug testing. We designed and fabricated a co-flow focusing, three-channel microfluidic device with a wide cell culture chamber. By controlling inlet flow rates of sample and two side solutions, we could generate hydrodynamic focusing and shifting that mediated precise regulation of the path and width of reagent and drug stream in the microfluidic device. We successfully validated a hydrodynamic focusing and shifting approach for spatially selective delivery of DiI, a lipophilic fluorophore, and doxorubicin, a chemotherapeutic agent, to tumor cells in our device. Moreover, subsequent flowing of a trypsin EDTA solution over the cells that were exposed to doxorubicin flow allowed us to selectively collect the treated cells. Our approach enabled downstream high-resolution microscopy of the cell suspension to confirm the nuclear delivery of doxorubicin into the tumor cells. In the device, we could also evaluate in situ the cytotoxic effect of doxorubicin to the tumor cells that were selectively treated by hydrodynamic flow focusing and shifting. These results show that hydrodynamic focusing and shifting enable a fast and robust approach to spatially treat and then collect cells in an optimized microfluidic device, offering an integrative assay tool for efficient drug screening and discovery.
流体力聚焦技术能够轻松地产生和控制层流,从而促进了现有微流控培养装置中细胞的药物治疗。然而,要将此类装置的应用扩展到多参数药物测试中,就必须解决当前流体力聚焦微流控技术的关键限制。在这里,我们描述了流体力聚焦和转移作为一种先进的微流控工具,用于空间选择性药物输送和整合基于细胞的药物测试。我们设计并制造了一种具有宽大细胞培养腔的共流聚焦、三通道微流控装置。通过控制样品和两个侧流的入口流速,我们可以产生流体力聚焦和转移,从而精确调节微流控装置中试剂和药物流的路径和宽度。我们成功地验证了一种流体力聚焦和转移方法,用于在我们的装置中对肿瘤细胞进行空间选择性地输送 DiI(一种亲脂性荧光染料)和阿霉素(一种化疗药物)。此外,随后将含有胰蛋白酶 EDTA 的溶液流过暴露于阿霉素流的细胞,使我们能够选择性地收集处理后的细胞。我们的方法使我们能够对细胞悬浮液进行下游高分辨率显微镜检查,以确认阿霉素核内递送到肿瘤细胞中。在该装置中,我们还可以原位评估阿霉素对通过流体力聚焦和转移选择性处理的肿瘤细胞的细胞毒性作用。这些结果表明,流体力聚焦和转移能够快速有效地实现空间处理,然后在优化的微流控装置中收集细胞,为高效药物筛选和发现提供了一种整合的分析工具。