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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Chen, Yong
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Publications (8/8 displayed)
- 2024Customizable Three-Dimensional Printed Earring Tap for Treating Affections Caused by Aesthetic Perforationscitations
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- 2019Low-velocity impact behaviour of woven laminate plates with fire retardant resincitations
- 2015MicroStructure Element Method (MSEM): viscous flow model for the virtual draw of microstructured optical fiberscitations
- 2015Accurate modelling of fabricated hollow-core photonic bandgap fiberscitations
- 2014The wear of PEEK in rolling–sliding contact : Simulation of polymer gear applications
- 2014X-ray tomography for structural analysis of microstructured and multimaterial optical fibers and preformscitations
- 2010Fabrication of ZnO micro- and nano-structures by electrodeposition using nanoporous and lithography defined templatescitations
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article
Customizable Three-Dimensional Printed Earring Tap for Treating Affections Caused by Aesthetic Perforations
Abstract
<jats:p>This work aimed to develop a three-dimensional (3D) wearable drug-loaded earring tap to treat affections caused by aesthetic perforations. The initial phase involved a combination of polymers to prepare filaments for fused deposition modeling (FDM) 3D printing using a centroid mixture design. Optimized filament compositions were used in the second phase to produce 3D printed earring taps containing the anti-inflammatory naringenin. Next, samples were assessed via physicochemical assays followed by in vitro skin permeation studies with porcine ear skin. Two filament compositions were selected for the study’s second phase: one to accelerate drug release and another with slow drug dissolution. Both filaments demonstrated chemical compatibility and amorphous behavior. The use of the polymer blend to enhance printability has been confirmed by rheological analysis. The 3D devices facilitated naringenin skin penetration, improving drug recovery from the skin’s most superficial layer (3D device A) or inner layers (3D device B). Furthermore, the devices significantly decreased transdermal drug delivery compared to the control containing the free drug. Thus, the resulting systems are promising for producing 3D printed earring taps with topical drug delivery and reinforcing the feasibility of patient-centered drug administration through wearable devices.</jats:p>