Abstract

Microfluidic devices fabricated via soft lithography have demonstrated compelling applications such as lab-on-a-chip diagnostics, DNA microarrays, and cell-based assays. These technologies could be further developed by directly integrating microfluidics with electronic sensors and curvilinear substrates as well as improved automation for higher throughput. Current additive manufacturing methods, such as stereolithography and multi-jet printing, tend to contaminate substrates with uncured resins or supporting materials during printing. Here, we present a printing methodology based on precisely extruding viscoelastic inks into self-supporting microchannels and chambers without requiring sacrificial materials. We demonstrate that, in the submillimeter regime, the yield strength of the as-extruded silicone ink is sufficient to prevent creep within a certain angular range. Printing toolpaths are specifically designed to realize leakage-free connections between channels and chambers, T-shaped intersections, and overlapping channels. The self-supporting microfluidic structures enable the automatable fabrication of multifunctional devices, including multimaterial mixers, microfluidic-integrated sensors, automation components, and 3D microfluidics.

Highlights

  • Microfluidic devices have the potential to enable transformational approaches for conducting microliter-scale chemical and biological research because of the advantages of small sample volumes and well-controlled microenvironments [1]

  • Our hypothesis was that self-supporting walls can be printed with the extrusion-based 3D printing method via carefully designed filament stacking orientations, e.g., straight or circular, on the cross-sectional planes (Fig. 1A)

  • The walls merged at the top and formed hollow channels and chambers with targeted geometries specified by the printing toolpath in the X-Y plane, such as the triangular/circular channels and hexagonal/conical domes illustrated in the bottom panel of Fig. 1A

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Summary

Introduction

Microfluidic devices have the potential to enable transformational approaches for conducting microliter-scale chemical and biological research because of the advantages of small sample volumes and well-controlled microenvironments [1]. They have demonstrated exciting applications in areas such as lab-on-a-chip diagnostics [2], point-of-care systems [3], organ replication on a chip [4], and bioassays [5]. The two most widely used methodologies for the fabrication of microfluidic devices are soft lithography and additive manufacturing. Because of the potential for contamination from either uncured residual resin in the channel voids or the sacrificial

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