Inexpensive, rapid prototyping of microfluidic devices using overhead transparencies and a laser print, cut and laminate fabrication method
This protocol is for generating microfluidic prototypes useful for biochemical assays using a print (printer toner on transparency sheets), cut (with a CO 2 laser cutter) and laminate (with a standard office laminator) approach. We describe a technique for fabricating microfluidic devices with compl...
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Veröffentlicht in: | Nature protocols 2015-06, Vol.10 (6), p.875-886 |
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Sprache: | eng |
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Zusammenfassung: | This protocol is for generating microfluidic prototypes useful for biochemical assays using a print (printer toner on transparency sheets), cut (with a CO
2
laser cutter) and laminate (with a standard office laminator) approach.
We describe a technique for fabricating microfluidic devices with complex multilayer architectures using a laser printer, a CO
2
laser cutter, an office laminator and common overhead transparencies as a printable substrate via a laser print, cut and laminate (PCL) methodology. The printer toner serves three functions: (i) it defines the microfluidic architecture, which is printed on the overhead transparencies; (ii) it acts as the adhesive agent for the bonding of multiple transparency layers; and (iii) it provides, in its unmodified state, printable, hydrophobic 'valves' for fluidic flow control. By using common graphics software, e.g., CorelDRAW or AutoCAD, the protocol produces microfluidic devices with a design-to-device time of ∼40 min. Devices of any shape can be generated for an array of multistep assays, with colorimetric detection of molecular species ranging from small molecules to proteins. Channels with varying depths can be formed using multiple transparency layers in which a CO
2
laser is used to remove the polyester from the channel sections of the internal layers. The simplicity of the protocol, availability of the equipment and substrate and cost-effective nature of the process make microfluidic devices available to those who might benefit most from expedited, microscale chemistry. |
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ISSN: | 1754-2189 1750-2799 |
DOI: | 10.1038/nprot.2015.051 |