Central Research Laboratories, Sysmex Corporation, 4-4-4 Takatsukadai, Nishi-ku, Kobe 651-2271, Japan.
Lab Chip. 2021 Aug 21;21(16):3112-3127. doi: 10.1039/d1lc00298h. Epub 2021 Jul 21.
There is an increasing need for the enrichment of rare cells in the clinical environments of precision medicine, personalized medicine, and regenerative medicine. With the possibility of becoming the next-generation cell sorters, microfluidic fluorescence-activated cell sorting (μ-FACS) devices have been developed to avoid cross-contamination, minimize device footprint, and eliminate bio-aerosols. However, due to highly precise flow control, the achievable throughput of the μ-FACS system is generally lower than the throughput of conventional FACS devices. Here, we report a fully integrated high-throughput microfluidic circulatory fluorescence-activated cell sorting (μ-CFACS) system for the enrichment of clinical rare cells. A microfluidic sorting cartridge has been developed for enriching samples through a sequential sorting process, which was further realized by the integration of both fast amplified piezoelectrically actuated on-chip valves and compact pneumatic cylinders actuated on-chip valves. At an equivalent throughput of ∼8000 events per second (eps), the purity of rare fluorescent microparticles has been significantly increased from ∼0.01% to ∼27.97%. An enrichment of ∼9400-fold from 0.009% to 81.86% has also been demonstrated for isolating fluorescently labelled MCF-7 breast cancer cells from Jurkat cells at an equivalent sorting throughput of ∼6400 eps. With the advantages of high throughput and contamination-free design, the proposed integrated μ-CFACS system provides a new option for the enrichment of clinical rare cells.
在精准医学、个性化医疗和再生医学的临床环境中,对稀有细胞的富集提出了更高的要求。由于有可能成为下一代细胞分选器,微流控荧光激活细胞分选(μ-FACS)设备已被开发出来,以避免交叉污染、最小化设备占地面积并消除生物气溶胶。然而,由于需要高度精确的流量控制,μ-FACS 系统的可达吞吐量通常低于传统 FACS 设备的吞吐量。在这里,我们报告了一种用于富集临床稀有细胞的完全集成的高通量微流循环荧光激活细胞分选(μ-CFACS)系统。已经开发了一种微流分选盒,通过顺序分选过程来富集样品,这是通过快速放大的压电驱动片上阀和紧凑的气动驱动片上阀的集成来实现的。在等效吞吐量约为 8000 个事件每秒(eps)的情况下,稀有荧光微球的纯度已从约 0.01%显著提高到约 27.97%。从 Jurkat 细胞中分离荧光标记的 MCF-7 乳腺癌细胞时,也实现了约 9400 倍的富集,从 0.009%到 81.86%,等效分选吞吐量约为 6400 eps。该集成的 μ-CFACS 系统具有高通量和无污染设计的优点,为临床稀有细胞的富集提供了一种新的选择。