Kim Jeeyong, Lim Hyunjung, Jee Hyunseul, Choo Seunghee, Yang Minji, Park Sungha, Lee Kyounghwa, Park Hyoungsook, Lim Chaeseung, Nam Jeonghun
Department of Laboratory Medicine, College of Medicine, Korea University, Seoul 08307, Korea.
Department of Obstetrics and Gynecology, College of Medicine, Korea University, Seoul 08307, Korea.
Micromachines (Basel). 2021 Jun 9;12(6):677. doi: 10.3390/mi12060677.
Cell concentration is a critical process in biological assays and clinical diagnostics for the pre-treatment of extremely rare disease-related cells. The conventional technique for sample preconcentration and centrifugation has the limitations of a batch process requiring expensive and large equipment. Therefore, a high-throughput continuous cell concentration technique needs to be developed. However, in single-pass operation, the required concentration ratio is hard to achieve. In this study, we propose a closed-loop continuous cell concentration system using a viscoelastic non-Newtonian fluid. For miniaturized and integrated systems, two piezoelectric pumps were adopted. The pumping capability generated by a piezoelectric pump in a microfluidic channel was evaluated depending on the applied voltage, frequency, sample viscosity, and channel length. The concentration performance of the device was evaluated using 13 μm particles and white blood cells (WBCs) with different channel lengths and voltages. In the closed-loop system, the focused cells collected at the center outlet were sent back to the inlet, while the buffer solution was removed to the side outlets. Finally, to expand the clinical applicability of our closed-loop system, WBCs in lysed blood samples with 70% hematocrit and prostate cancer cells in urine samples were used. Using the closed-loop system, WBCs were concentrated by 63.4 ± 0.8-fold within 20 min to a final volume of 160 μL using 10 mL of lysed blood sample with 70% hematocrit (3 cP). In addition, prostate cancer cells in 10 mL urine samples were concentrated by 64.1-fold within ~11 min due to low viscosity (1 cP).
细胞浓缩是生物检测和临床诊断中对极其罕见的疾病相关细胞进行预处理的关键过程。传统的样品预浓缩和离心技术存在批量处理的局限性,需要昂贵且大型的设备。因此,需要开发一种高通量连续细胞浓缩技术。然而,在单通道操作中,所需的浓缩比很难实现。在本研究中,我们提出了一种使用粘弹性非牛顿流体的闭环连续细胞浓缩系统。对于小型化和集成系统,采用了两个压电泵。根据施加的电压、频率、样品粘度和通道长度,评估了微流控通道中压电泵产生的泵送能力。使用13μm颗粒和不同通道长度及电压的白细胞(WBC)评估了该装置的浓缩性能。在闭环系统中,在中心出口收集的聚焦细胞被送回入口,而缓冲溶液则被排到侧出口。最后,为了扩大我们闭环系统的临床适用性,使用了血细胞比容为70%的溶血血液样本中的白细胞和尿液样本中的前列腺癌细胞。使用闭环系统,在20分钟内,使用10mL血细胞比容为70%(约3cP)的溶血血液样本,白细胞被浓缩了约63.4±0.8倍,最终体积为160μL。此外,由于尿液样本粘度较低(约1cP),10mL尿液样本中的前列腺癌细胞在约11分钟内被浓缩了约64.1倍。