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Updated: Feb 28, 2026

Fabrication of Engineered Vascular Flaps Using 3D Printing Technologies
Published on: May 19, 2022
3D-Printed PLDLA-TMC/PEG 400 Vascular Scaffolds with a Poly(hexamethylene Biguanide) Antibacterial Coating
Monique M Munhoz1, Flavia Pedrini2, Cecilia T de Barros2
1Post-Graduation Program of Biomaterials and Regenerative Medicine (PPGBMR), Surgery Department, Faculty of Medical and Health Sciences, Pontifical Catholic University of São Paulo, Sorocaba 18060-030, São Paulo, Brazil.
This study presents improved 3D-printed vascular scaffolds using poly(L-co-D,L-lactide)-poly(trimethylene carbonate) with polyethylene glycol and poly(hexamethylene biguanide) for enhanced mechanical properties and antibacterial activity.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Polymer Chemistry
Background:
- Synthetic vascular scaffolds often have poor mechanical strength and low hydrophilicity.
- These limitations hinder vascular integration and increase infection risk.
- Developing advanced scaffolds is crucial for effective vascular repair.
Purpose of the Study:
- To engineer 3D-printed poly(L-co-D,L-lactide)-poly(trimethylene carbonate) scaffolds with enhanced mechanical and antibacterial properties.
- To incorporate polyethylene glycol (PEG) for improved hydrophilicity and mechanical modulation.
- To coat scaffolds with poly(hexamethylene biguanide) (PHMB) for sustained antimicrobial release and efficacy.
Main Methods:
- Fabrication of 3D-printed PLDLA-TMC scaffolds with varying PEG 400 concentrations.
- Application of PHMB coatings at 3%, 6%, and 12% concentrations within HPMC.
- Characterization of structural, thermal, mechanical, and antimicrobial properties.
- Evaluation of drug release kinetics, cytotoxicity, and biocompatibility in co-cultures.
Main Results:
- 2% PEG incorporation significantly increased tensile strength to 0.79 MPa and improved elasticity.
- A 6% PHMB coating demonstrated sustained release over 7 days, maintained cell viability (72.95%), and achieved a 13.1 mm inhibition zone against S. aureus.
- 12% PHMB coating induced cytotoxicity, while 3% showed burst release.
Conclusions:
- Optimized 3D-printed PLDLA-TMC scaffolds with 2% PEG and 6% PHMB offer superior mechanical performance.
- These scaffolds exhibit sustained antimicrobial release and potent antibacterial activity.
- The developed scaffolds demonstrate promising biocompatibility for in vitro vascular applications.
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