Surface-micromachined parylene dual valves for on-chip unpowered microflow regulation

被引:31
作者
Chen, Po-Jui [1 ]
Rodger, Damien C.
Meng, Ellis M.
Humayun, Mark S.
Tai, Yu-Chong
机构
[1] CALTECH, Dept Elect Engn, Pasadena, CA 91125 USA
[2] CALTECH, Dept Bioengn, Div Engn & Appl Sci, Pasadena, CA 91125 USA
[3] Univ So Calif, Keck Sch Med, Los Angeles, CA 90033 USA
[4] Univ So Calif, Viterbi Sch Engn, Dept Biomed Engn, Los Angeles, CA 90089 USA
基金
美国国家科学基金会;
关键词
microflow control; microfluidics; microvalve; parylene;
D O I
10.1109/JMEMS.2006.889534
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
This paper presents the world's first surface-micromachined parylene dual-valved microfluidic system for on-chip unpowered microflow regulation. Incorporating a normally closed and a normally open passive check valve in a back-to-back configuration inside a microchannel, the dual-valved system has successfully regulated the pressure/flow rate of air and liquid without power consumption or electronic/magnetic/thermal transduction. By exclusively using parylene C (poly-para-xylylene C) as the structural material, the fabricated valves have higher flexibility to shunt flows in comparison to other conventional thin-film valves. A state-of-the-art multilayer polymer surface-micromachining technology is applied here to fabricate parylene microvalves of various designs. The parylene-based devices are completely biocompatible/implantable and provide an economical paradigm for fluidic control in integrated lab-on-a-chip systems. Design, fabrication, and characterization of the parylene dual valves are discussed in this paper. Testing results have successfully demonstrated that the microflow regulation of the on-chip dual-valved system can achieve a bandpass profile in which the pressure control range is 0-50 mmHg with corresponding flow rates up to 2 mL/min for air flow and 1 mu L/min flow rate for water flow. This regulation range is suitable for controlling biological conditions in human health care, with potential applications including drug delivery and regulation of elevated intraocular pressure (IOP) in glaucoma patients.
引用
收藏
页码:223 / 231
页数:9
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