TY - JOUR
T1 - Single-step fabrication of computationally designed microneedles by continuous liquid interface production
AU - Johnson, Ashley R.
AU - Caudill, Cassie L.
AU - Tumbleston, John R.
AU - Bloomquist, Cameron J.
AU - Moga, Katherine A.
AU - Ermoshkin, Alexander
AU - Shirvanyants, David
AU - Mecham, Sue J.
AU - Luft, J. Christopher
AU - De Simone, Joseph M.
N1 - Funding Information:
The authors would like to acknowledge the Defense Threat Reduction Agency (HDTRA1 -13-1-0045) and Carbon for supporting this research. Bob Pinschmidt, Rima Janusziewicz and Adam Quintanilla are acknowledged for their contributions to useful scientific discussions. Competing interest declaration: I have read the journal’s policy and authors JRT, DS, AE, and JMD all have an equity stake in Carbon, Inc., which is a venture-backed startup company. This does not alter our adherence to PLOS One policies on data sharing and materials.
Publisher Copyright:
© 2016 Johnson et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2016/9
Y1 - 2016/9
N2 - Microneedles, arrays of micron-sized needles that painlessly puncture the skin, enable transdermal delivery of medications that are difficult to deliver using more traditional routes. Many important design parameters, such as microneedle size, shape, spacing, and composition, are known to influence efficacy, but are notoriously difficult to alter due to the complex nature of microfabrication techniques. Herein, we utilize a novel additive manufacturing ("3D printing") technique called Continuous Liquid Interface Production (CLIP) to rapidly prototype sharp microneedles with tuneable geometries (size, shape, aspect ratio, spacing). This technology allows for mold-independent, one-step manufacturing of microneedle arrays of virtually any design in less than 10 minutes per patch. Square pyramidal CLIP microneedles composed of trimethylolpropane triacrylate, polyacrylic acid and photopolymerizable derivatives of polyethylene glycol and polycaprolactone were fabricated to demonstrate the range of materials that can be utilized within this platform for encapsulating and controlling the release of therapeutics. These CLIP microneedles effectively pierced murine skin ex vivo and released the fluorescent drug surrogate rhodamine.
AB - Microneedles, arrays of micron-sized needles that painlessly puncture the skin, enable transdermal delivery of medications that are difficult to deliver using more traditional routes. Many important design parameters, such as microneedle size, shape, spacing, and composition, are known to influence efficacy, but are notoriously difficult to alter due to the complex nature of microfabrication techniques. Herein, we utilize a novel additive manufacturing ("3D printing") technique called Continuous Liquid Interface Production (CLIP) to rapidly prototype sharp microneedles with tuneable geometries (size, shape, aspect ratio, spacing). This technology allows for mold-independent, one-step manufacturing of microneedle arrays of virtually any design in less than 10 minutes per patch. Square pyramidal CLIP microneedles composed of trimethylolpropane triacrylate, polyacrylic acid and photopolymerizable derivatives of polyethylene glycol and polycaprolactone were fabricated to demonstrate the range of materials that can be utilized within this platform for encapsulating and controlling the release of therapeutics. These CLIP microneedles effectively pierced murine skin ex vivo and released the fluorescent drug surrogate rhodamine.
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U2 - 10.1371/journal.pone.0162518
DO - 10.1371/journal.pone.0162518
M3 - Article
C2 - 27607247
AN - SCOPUS:84990997758
SN - 1932-6203
VL - 11
JO - PLoS One
JF - PLoS One
IS - 9
M1 - e0162518
ER -