Selective laser ablation for in situ fabrication of enclosed channel porous-media microfluidic analytical devices

被引:6
|
作者
Sumantakul, Saichon [1 ]
Remcho, Vincent T. [1 ]
机构
[1] Oregon State Univ, Dept Chem, Corvallis, OR 97331 USA
关键词
PAPER-BASED MICROFLUIDICS; FLOW; IMMUNOASSAY; CHOLESTEROL; DIAGNOSTICS; LPAD;
D O I
10.1039/d3lc00208j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This work describes a new method for fabrication of enclosed channel porous-media microfluidic analytical devices using selective laser ablation. Microfluidic structures can be readily produced inside the enclosed devices within two fabrication steps. A sheet of porous material was first sandwiched and bonded between two sheets of polymeric film. The porous substrate inside the film layers was then selectively ablated using a laser cutter to create hollow barriers for microfluidic channels. Selective ablation of only the porous layer was achieved because the porous substrate layer is susceptible to ablation by the laser beam, whereas the film layer is resistant to laser ablation due to its light transmission properties. This selective laser ablation processing is not limited by laser type. As a proof-of-concept, two different laser systems, a 10.6 mu m CO2 laser and a 455 nm diode laser, were employed for this purpose. A variety of porous materials, including cellulose, nitrocellulose, and glass microfiber, were combined with a wide variety of polymeric films to fabricate enclosed microfluidic devices. The developed method is versatile; depending on material combination and number of layers of materials in the devices, enclosed microfluidic devices with 2D, passive 3D, or compression-activated 3D fluid flow can be created. Quantitative assays for albumin, glucose, and cholesterol in human serum performed using devices produced via this method demonstrated the utility of this fabrication approach. This unique, simple, and scalable method for fabrication of enclosed microfluidic devices not only ensures protection of devices from contamination and prevention of fluid evaporation, but also offers a method for commercial fabrication of porous-media analytical devices.
引用
收藏
页码:3194 / 3206
页数:14
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