Micromachining in plastics using X-ray lithography for the fabrication of micro-electrophoresis devices

被引:71
作者
Ford, SM
Davies, J
Kar, B
Qi, SD
McWhorter, S
Soper, SA [1 ]
Malek, CK
机构
[1] Louisiana State Univ, Dept Chem, Baton Rouge, LA 70803 USA
[2] Louisiana State Univ, Ctr Adv Microstruct & Devices, Baton Rouge, LA 70810 USA
来源
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME | 1999年 / 121卷 / 01期
关键词
D O I
10.1115/1.2798035
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Micromachining was performed in polymethylmethacrylate (PMMA) using X-ray lithography for the fabrication of miniaturized devices (microchips) for potential applications in chemical and genetic analyses. The devices were fabricated using two different techniques: transfer mask technology and a Kapton(R) mask. For both processes, the channel topography was transferred (1:1) to the appropriate substrate via the use of art optical mask. In the case of the transfer mask technique, the PMMA substrate was coated with a positive photoresist and a thin Au/Cr plating base. Following UV exposure, the resist was developed and a thick overlayer (similar to 3 mu m) of Au electroplated onto the PMMA substrate only where the resist was removed, which acted as an absorber of the X-rays. In the other technique, a Kapton(R) film was used as the X-ray mask. In this case, the Kapton(R) film was UV exposed using the optical mask to define the channel topography and following development of the resist, a thick Au overlayer (8 mu m) was electrodeposited onto the Kapton(R) sheet. The PMMA wafer during X-ray exposure was situated directly underneath the Kapton(R) mask. In both cases, the PMMA wafer was exposed to soft X-rays and developed to remove the exposed PMMA. The resulting channels were found to be 20 mu m in width (determined by optical mask) with channel depths of similar to 50 mu m (determined by x-ray exposure time). In order to demonstrate the utility of this micromachining process, several components were fabricated in PMMA including capillary/chip connectors, injectors for fixed-volume sample introduction, separation channels for electrophoresis and integrated fiber optic fluorescence detectors. These components could be integrated into a single device to assemble a system appropriate for the rapid analysis of various targets.
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收藏
页码:13 / 21
页数:9
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