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Method Article

One-Step Approach to Fabricating Polydimethylsiloxane Microfluidic Channels of Different Geometric Sections by Sequential Wet Etching Processes

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DOI:

10.3791/57868

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September 13th, 2018

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In This Article

Summary

Several methods are available for the fabrication of channels of non-rectangular sections embedded in polydimethylsiloxane microfluidic devices. Most of them involve multistep manufacturing and extensive alignment. In this paper, a one-step approach is reported for fabricating microfluidic channels of different geometric cross sections by polydimethylsiloxane sequential wet etching.

Abstract

Polydimethylsiloxane (PDMS) materials are substantially exploited to fabricate microfluidic devices by using soft lithography replica molding techniques. Customized channel layout designs are necessary for specific functions and integrated performance of microfluidic devices in numerous biomedical and chemical applications (e.g., cell culture, biosensing, chemical synthesis, and liquid handling). Owing to the nature of molding approaches using silicon wafers with photoresist layers patterned by photolithography as master molds, the microfluidic channels commonly have regular cross sections of rectangular shapes with identical heights. Typically, channels with multiple heights or different geometric sections are designed to possess particular functions and to perform in various microfluidic applications (e.g., hydrophoresis is used for sorting particles and in continuous flows for separating blood cells6,7,8,9). Therefore, a great deal of effort has been made in constructing channels with various sections through multiple-step approaches like photolithography using several photoresist layers and assembly of different PDMS thin sheets. Nevertheless, such multiple-step approaches usually involve tedious procedures and extensive instrumentation. Furthermore, the fabricated devices may not perform consistently and the resulted experimental data may be unpredictable. Here, a one-step approach is developed for the straightforward fabrication of microfluidic channels with different geometric cross sections through PDMS sequential wet etching processes, that introduces etchant into channels of planned single-layer layouts embedded in PDMS materials. Compared to the existing methods for manufacturing PDMS microfluidic channels with different geometries, the developed one-step approach can significantly simplify the process to fabricate channels with non-rectangular sections or various heights. Consequently, the technique is a way of constructing complex microfluidic channels, which provides a fabrication solution for the advancement of innovative microfluidic systems.

Introduction

Microfluidic techniques have drawn attention over the past decades because of their intrinsic advantages for a variety of biomedical and chemical research and applications. Several material usage options for constructing microfluidic chips are available nowadays, such as polymers, ceramics, and silicon materials. To the best of our knowledge, among the microfluidic materials, PDMS is the most common one due to its appropriate material properties for various microfluidics research and applications, including its optical and biological compatibilities with particles, fluids, and extremely small living organisms1,2

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Protocol

1. Fabrication of Microfluidic Devices with Single-Layer Channel Layouts

NOTE: In this paper, the soft lithography method3 is adopted for fabricating microfluidic devices made of PDMS materials, to demonstrate how to manufacture channels with various sections.

  1. Creation of master molds for a PDMS layer with designed topology features
    1. Design channel layouts on a PDMS layer for a single etching process or etching in sequence.
    2. Sketch the inverted topology features of the designed PDMS layer using a computer-aided drawing program.
    3. Deliver the sketch file to a ....

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Results

Recently, a large number of studies have been made on the fabrication of microfluidic devices with channels of different sections by lithography replica molding13,14,15 and PDMS etching techniques17,18,19,20,21,

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Discussion

Over the past decades, microfluidics has offered promising means by which experimental platforms for chemical and biomedical research can be constructed systematically1,2,3,4,5. The platforms have also presented their capabilities of investigating several cellular functions in vivo under physiological microenvironment conditions via in vitro .......

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Disclosures

The authors have nothing to declare.

Acknowledgements

The authors gratefully acknowledge the support provided by the National Health Research Institutes (NHRI) in Taiwan under the Innovative Research Grant (IRG) (EX106-10523EI), the Taiwan Ministry of Science and Technology (MOST 104-2218-E-032-004, 104-2221-E-001-015-MY3, 105-2221-E-001-002-MY2, 105-2221-E-032-006, 106-2221-E-032-018-MY2), and the Academia Sinica Career Development Award. The authors would like to thank Heng-Hua Hsu for proofreading the manuscript.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
1-Methyl-2-PyrrolidinoneTedia, Fairfield, OHME-1962NMP
10 ml SyringeBecton-Dickinson, Franklin Lakes, NJ302151
150 mm Petri dishDogger ScienceDP-43151
1H,1H,2H,2H- PerfluorooctyltrichlorosilaneAlfa Aesar, Ward Hill, MAL1660697 % silane 
4'' Silicon Dummy WaferWollemi Technical, Taoyuan, Taiwan-
AcetoneECHO Chemical, Miaoli, TaiwanAH3102-000000-72EC
AG Double Expose Mask AlignerM&R Nano Technology, Taoyuan, TaiwanAG500-4D-D-V-S-H
Biopsy PunchMiltex, Plainsboro, NJ33-31
Blunt NeedleJensen Global, Santa Barbara, CAGauge 16
Buffered Oxide EtchECHO Chemical, Miaoli, TaiwanPH3101-000000-72EC
DesicattorA-VAC Industries, Anaheim, CA35.10001.01
Fluorescein Sodium Salt WaterSigma-Aldrich Co., St Louis, MOF6300
ImageJNational Institutes of Health, Bethesda, MDVer. 1.51Imaging Processing Program 
Inverted Fluorescence Microscope Leica Microsystems, Wetzlar, GermanyDMI 6000 B
Isopropyl Alcohol (IPA)ECHO Chemical, Miaoli, TaiwanCMOS112-00000-72EC
Leica Application Suite Leica Microsystems GmbHLAS X
MATLABMathWorks, Natick, MAR2015bProgramming for MR evaluation
Mechanical Convention OvenThermoFisher Scientific,Waltham, MALindberg Blue M MO1450C
Plasma Tretment SystemNordson MARCH, Concord CAPX-250Oxygen plasma surface treatment
Polydimehtylsiloxane (PDMS) Dow Corning, Midland, MISYLGARD 184
Polyethylene TubingBecton-Dickinson and Company, Sparks, MD427446PE 205, 10'
Spin CoaterELS Technology, Hsinchu, TaiwanELS 306MA
Negative Tone Photoresist MicroChem, Westborough, MASU-8 2050
Negative Tone Photoresist DeveloperMicroChem, Westborough, MAY020100SU-8 Developer
Surgical BladeFeather, Osaka, Japan5005093PDMS cutting
Syringe PumpChemyx, Houston, TXFusion 400
Tetra-n-butylammonium Fluoride (TBAF)Alfa Aesar, Ward Hill, MAA10588

References

  1. Tung, Y. -C., et al. Optofluidic Detection for Cellular Phenotyping. Lab on a Chip. 12, 3552-3565 (2012).
  2. Lu, Y., Yang, L., Wei, W., Shi, Q. Microchip-based Single-cell Functional Proteomics for Biomedical Applications. Lab on a Chip. 17, 1250-1263 (201....

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