School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
The Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Lab Chip. 2024 Jan 17;24(2):197-209. doi: 10.1039/d3lc00957b.
This paper introduces a two-inlet, one-outlet lung-on-a-chip device with semi-circular cross-section microchannels and computer-controlled fluidic switching that enables a broader systematic investigation of liquid plug dynamics in a manner relevant to the distal airways. A leak-proof bonding protocol for micro-milled devices facilitates channel bonding and culture of confluent primary small airway epithelial cells. Production of liquid plugs with computer-controlled inlet channel valving and just one outlet allows more stable long-term plug generation and propagation compared to previous designs. The system also captures both plug speed and length as well as pressure drop concurrently. In one demonstration, the system reproducibly generates surfactant-containing liquid plugs, a challenging process due to lower surface tension that makes the plug formation less stable. The addition of surfactant decreases the pressure required to initiate plug propagation, a potentially significant effect in diseases where surfactant in the airways is absent or dysfunctional. Next, the device recapitulates the effect of increasing fluid viscosity, a challenging analysis due to higher resistance of viscous fluids that makes plug formation and propagation more difficult particularly in airway-relevant length scales. Experimental results show that increased fluid viscosity decreases plug propagation speed for a given air flow rate. These findings are supplemented by computational modeling of viscous plug propagation that demonstrates increased plug propagation time, increased maximum wall shear stress, and greater pressure differentials in more viscous conditions of plug propagation. These results match physiology as mucus viscosity is increased in various obstructive lung diseases where it is known that respiratory mechanics can be compromised due to mucus plugging of the distal airways. Finally, experiments evaluate the effect of channel geometry on primary human small airway epithelial cell injury in this lung-on-a-chip. There is more injury in the middle of the channel relative to the edges highlighting the role of channel shape, a physiologically relevant parameter as airway cross-sectional geometry can also be non-circular. In sum, this paper describes a system that pushes the device limits with regards to the types of liquid plugs that can be stably generated for studies of distal airway fluid mechanical injury.
本文介绍了一种具有半圆形横截面微通道和计算机控制的流体切换的双入口单出口肺芯片设备,能够以与远端气道相关的方式更广泛地系统研究液塞动力学。一种用于微加工设备的防漏键合协议促进了通道键合和融合的原代小气道上皮细胞培养。通过计算机控制的入口通道阀和一个出口来产生液塞,可以与以前的设计相比,更稳定地产生和传播长期的液塞。该系统还可以同时捕获塞子速度、长度和压降。在一个演示中,该系统可重复地生成含有表面活性剂的液塞,这是一个具有挑战性的过程,因为表面张力较低会使塞子形成不太稳定。表面活性剂的添加会降低引发塞子传播所需的压力,这在气道中缺乏或功能失调的表面活性剂的疾病中可能是一个重要的潜在影响。接下来,该设备再现了增加流体粘度的效果,这是一个具有挑战性的分析,因为粘性流体的阻力较大,使得塞子的形成和传播更加困难,特别是在与气道相关的长度尺度上。实验结果表明,对于给定的气流速率,增加流体粘度会降低塞子的传播速度。这些发现得到了粘性塞子传播计算模型的补充,该模型表明在更粘性的塞子传播条件下,塞子传播时间增加,最大壁面剪切应力增加,压力差增大。这些结果与生理学相符,因为在各种阻塞性肺病中,粘液粘度增加,已知由于远端气道的粘液阻塞,呼吸力学可能会受到影响。最后,实验评估了通道几何形状对该肺芯片中原代人小气道上皮细胞损伤的影响。与边缘相比,通道中间的损伤更大,突出了通道形状的作用,这是一个生理相关的参数,因为气道的横截面几何形状也可能不是圆形的。总之,本文描述了一种系统,该系统在能够稳定产生用于研究远端气道液力损伤的液塞类型方面推动了设备极限。