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You are researching: Warsaw University of Technology
Cell Type
Tissue and Organ Biofabrication
Skin Tissue Engineering
Drug Delivery
Biological Molecules
Solid Dosage Drugs
Stem Cells
Personalised Pharmaceuticals
Inducend Pluripotent Stem Cells (IPSCs)
Drug Discovery
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All Groups
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- poly(octanediol-co-maleic anhydride-co-citrate) (POMaC)
- Poly(Oxazoline)
- 2-hydroxyethyl methacrylate (HEMA)
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- Cell Type
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- Organoids
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- Synoviocytes
- Keratinocytes
- Skeletal Muscle-Derived Cells (SkMDCs)
- Neurons
- Macrophages
- Human Trabecular Meshwork Cells
- Endothelial
- CardioMyocites
- Melanocytes
- Institution
- Chalmers University of Technology
- Karlsruhe institute of technology
- University of Freiburg
- Helmholtz Institute for Pharmaceutical Research Saarland
- Leipzig University
- University Hospital Basel
- AO Research Institute (ARI)
- Shanghai University
- Univerity of Hong Kong
- University of Toronto
- Brown University
- Polish Academy of Sciences
- University of Wurzburg
- Technical University of Dresden
- University of Nantes
- Montreal University
- Shandong Medical University
- University of Birmingham
- Institute for Bioengineering of Catalonia (IBEC)
- University of Michigan – School of Dentistry
- Myiongji University
- Harbin Institute of Technology
- Technical University of Berlin
- University of Amsterdam
- University of Tel Aviv
- University of Applied Sciences Northwestern Switzerland
- Anhui Polytechnic
- University Children's Hospital Zurich
- Bayreuth University
- Aschaffenburg University
- University of Michigan, Biointerfaces Institute
- Abu Dhabi University
- Jiao Tong University
- University of Aveiro
- Ghent University
- Chiao Tung University
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- University of Sheffield
- University of Michigan – Biointerfaces Institute
- Warsaw University of Technology
- National University of Singapore
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- DTU – Technical University of Denmark
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- Adolphe Merkle Institute Fribourg
- Halle-Wittenberg University
- Baylor College of Medicine
- INM – Leibniz Institute for New Materials
- National Yang Ming Chiao Tung University
- University of Vilnius
- Zurich University of Applied Sciences (ZHAW)
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- ETH Zurich
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- Nanjing Medical University
- University of Bordeaux
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- DWI – Leibniz Institute
- Nanyang Technological University
- National Institutes of Health (NIH)
- Ningbo Institute of Materials Technology and Engineering (NIMTE)
- KU Leuven
- Politecnico di Torino
- Utrecht Medical Center (UMC)
- Rizzoli Orthopaedic Institute
- Queen Mary University
- Veterans Administration Medical Center
- University of Minnesota
- University of Manchester
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- University of Barcelona
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- ENEA
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- Biomaterials & Bioinks
- Application
- Bioelectronics
- Biomaterial Processing
- Tissue Models – Drug Discovery
- Industrial
- Drug Discovery
- In Vitro Models
- Robotics
- Electronics – Robotics – Industrial
- Medical Devices
- Tissue and Organ Biofabrication
- Adipose Tissue Engineering
- Trachea Tissue Engineering
- Ocular Tissue Engineering
- Intervertebral Disc (IVD) Tissue Engineering
- Muscle Tissue Engineering
- Liver tissue Engineering
- Cartilage Tissue Engineering
- Bone Tissue Engineering
- Dental Tissue Engineering
- Drug Delivery
- Urethra Tissue Engineering
- Skin Tissue Engineering
- Uterus Tissue Engineering
- Gastric Tissue Engineering
- Nerve – Neural Tissue Engineering
- Meniscus Tissue Engineering
- Heart – Cardiac Patches Tissue Engineering
- BioSensors
- Personalised Pharmaceuticals
- Review Paper
- Printing Technology
AUTHOR
Title
Drop-on-demand antimicrobial printed coatings loaded with dehydroabietic acid derivative to prevent orthopedic implant infections
[Abstract]
Year
2026
Journal/Proceedings
J. Mater. Chem. B
Reftype
DOI/URL
DOI
Groups
AbstractMicrovalve-based drop-on-demand (DOD) printing technology was applied to create antimicrobial coatings for orthopedic implants. Leveraging the high-precision deposition capabilities of DOD{,} coatings loaded with a novel biofilm inhibitor{,} N- (abiet-8{,}11{,}13-trien-18oyl) cyclohexyl-L-alanine (DHA1){,} were fabricated on titanium coupons. The PLGA-PEG-DHA1 coatings exhibited significant efficacy in preventing Staphylococcus aureus adhesion in monoand co-culture with HL-60 cells. Furthermore{,} the PLGA-PEG-DHA1 coatings showed a sustained protective effect of the 30% DHA1-loaded coating over 24 hours. The PLGA-PEG-DHA1 coatings ensured safety with no cytotoxic effect observed on SaOS-2 mammalian cells{,} fostering tissue integration post-implantation. This study paves the way to produce multi-component DOD coatings combining various ink compositions{,} including different polymers{,} antimicrobial agents{,} or growth factors.