A small-scale, rolled-membrane microfluidic artificial lung designed towards future large area manufacturing

被引:30
|
作者
Thompson, A. J. [1 ,2 ]
Marks, L. H. [1 ]
Goudie, M. J. [3 ]
Rojas-Pena, A. [2 ]
Handa, H. [3 ]
Potkay, J. A. [1 ,2 ]
机构
[1] VA Ann Arbor Healthcare Syst, Ann Arbor, MI 48105 USA
[2] Univ Michigan, Dept Surg, Ann Arbor, MI 48109 USA
[3] Univ Georgia, Coll Engn, Athens, GA 30602 USA
来源
BIOMICROFLUIDICS | 2017年 / 11卷 / 02期
关键词
SHEAR-STRESS; MICROCHANNEL TECHNOLOGIES; GAS-EXCHANGE; DEVICE; BLOOD; AGGREGATION; FLOW;
D O I
10.1063/1.4979676
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Artificial lungs have been used in the clinic for multiple decades to supplement patient pulmonary function. Recently, small-scale microfluidic artificial lungs (mu AL) have been demonstrated with large surface area to blood volume ratios, biomimetic blood flow paths, and pressure drops compatible with pumpless operation. Initial small-scale microfluidic devices with blood flow rates in the mu l/min to ml/min range have exhibited excellent gas transfer efficiencies; however, current manufacturing techniques may not be suitable for scaling up to human applications. Here, we present a new manufacturing technology for a microfluidic artificial lung in which the structure is assembled via a continuous "rolling" and bonding procedure from a single, patterned layer of polydimethyl siloxane (PDMS). This method is demonstrated in a small-scale four-layer device, but is expected to easily scale to larger area devices. The presented devices have a biomimetic branching blood flow network, 10 mu m tall artificial capillaries, and a 66 mu m thick gas transfer membrane. Gas transfer efficiency in blood was evaluated over a range of blood flow rates (0.1-1.25ml/min) for two different sweep gases (pure O-2, atmospheric air). The achieved gas transfer data closely follow predicted theoretical values for oxygenation and CO2 removal, while pressure drop is marginally higher than predicted. This work is the first step in developing a scalable method for creating large area microfluidic artificial lungs. Although designed for microfluidic artificial lungs, the presented technique is expected to result in the first manufacturing method capable of simply and easily creating large area microfluidic devices from PDMS.
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页数:12
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