Biodegradable polymer microneedle (MN) arrays are an emerging class of transdermal drug delivery devices that promise a painless and sanitary alternative to syringes; however, prototyping bespoke needle architectures is expensive and requires production of new master templates. Here, we present a new microfabrication technique for MNs using fused deposition modeling (FDM) 3D printing using polylactic acid, an FDA approved, renewable, biodegradable, thermoplastic material. We show how this natural degradability can be exploited to overcome a key challenge of FDM 3D printing, in particular the low resolution of these printers. We improved the feature size of the printed parts significantly by developing a post fabrication chemical etching protocol, which allowed us to access tip sizes as small as 1 μm. With 3D modeling software, various MN shapes were designed and printed rapidly with custom needle density, length, and shape. Scanning electron microscopy confirmed that our method resulted in needle tip sizes in the range of 1-55 μm, which could successfully penetrate and break off into porcine skin. We have also shown that these MNs have comparable mechanical strengths to currently fabricated MNs and we further demonstrated how the swellability of PLA can be exploited to load small molecule drugs and how its degradability in skin can release those small molecules over time.
Biodegradable polymer microneedle (MN) arrays are an
emerging class of transdermal drug delivery devices that promise a painless and
sanitary alternative to syringes; however, prototyping bespoke needle
architectures is expensive and requires production of new master templates.
Here, we present a new microfabrication technique for MNs using fused
deposition modeling (FDM) 3D printing using polylactic acid, an FDA approved,
renewable, biodegradable, thermoplastic material. We show how this natural
degradability can be exploited to overcome a key challenge of FDM 3D printing,
in particular the low resolution of these printers. We improved the feature
size of the printed parts significantly by developing a post fabrication
chemical etching protocol, which allowed us to access tip sizes as small as 1
μm. With 3D modeling software, various MN shapes were designed and printed
rapidly with custom needle density, length, and shape. Scanning electron
microscopy confirmed that our method resulted in needle tip sizes in the range of
1 – 55 µm, which could successfully penetrate and break off into porcine skin.
We have also shown that these MNs have comparable mechanical strengths to
currently fabricated MNs and we further demonstrated how the swellability of
PLA can be exploited to load small molecule drugs and how its degradability in
skin can release those small molecules over time.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.