Fear of needles is prevalent, estimated at around 10% in adults worldwide. We report on new solid microneedle arrays made of gold in combination with micro holes to replace traditional hypodermic needles for drug delivery. This work provides a breakthrough for painless drug delivery with precise control over the microneedle width, height, array density and position. Results show successful delivery of liquids through a parafilm layer representing the stratum corneum of the human skin.
Microneedles are an emerging technology that offer an alternative to traditional hypodermic needles for drug and vaccine delivery. Less than 1 mm in length, microneedles can penetrate the skin with little to no pain making them a suitable option for the 1-in-10 people that may avoid seeking medical care due to needle phobia. However, there are significant challenges with adapting existing microneedle fabrication methods for large scale manufacturing while matching the repeatability, reliability, and cost of current hypodermic needle mass production processes. In this work we present a novel method of fabricating microneedles using a modified automated wire bonding process that is highly suited for mass production due to existing widespread use of this process and equipment in the semiconductor industry. Microneedle arrays of different densities were fabricated on FR-4 based printed circuit board substrates using this automated process and tested by inserting into porcine skin tissue to determine insertion forces. The required insertion force generally increased with increasing array density due to the “bed of nails” effect and decreased with increasing insertion speed due to the viscoelastic properties of porcine skin tissue. Characterizing the correlations between insertion force, insertion speed, and array density are important for designing microneedle-based devices and applicators that can reliably penetrate skin. Microneedle arrays were also successfully created by automated wire bonding on polyimide-based printed circuit boards to demonstrate that this process can be done on flexible substrates. Further investigation with larger samples sizes is required to expand on the preliminary findings of this work.
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