Improving Infection Resistance in Tissue Engineered Scaffolds for Tensile Applications Using Vancomycin-Embedded Melt Electrowritten Scaffolds

, , , , & (2023) Improving Infection Resistance in Tissue Engineered Scaffolds for Tensile Applications Using Vancomycin-Embedded Melt Electrowritten Scaffolds. Macromolecular Materials and Engineering, 308(10), Article number: 2300168.

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Description

It is important to consider mechanical, biological, and antibacterial properties of scaffolds when used for tissue engineering applications. This study presents a method to create complex “wavy” architecture polycaprolactone (PCL) scaffolds toward the development of tissue engineered ligament and tendon tissue substitutes, fabricated using melt electrowriting (MEW) and loaded with vancomycin (5, 10, and 25% w/w). Scaffolds are characterized for both mechanical and biological properties. Loading PCL scaffolds with vancomycin with modified solvent evaporation technique achieves a high loading efficiency of maximum 18% w/w and high encapsulation efficiency with over 89%. Vancomycin loaded PCL scaffolds with all three doses (5, 10, and 25% w/w) display antibacterial activity against Gram-positive Staphylococcus aureus (S. aureus) up to 14 days of release. Initial burst followed by a sustained release is observed on all three vancomycin loaded scaffolds for up to 28 days. Importantly, in addition to antibacterial properties, vancomycin-loaded PCL scaffolds also display improved mechanical properties compared to traditional crosshatch design MEW scaffolds and are noncytotoxic at all concentrations as demonstrated by live-dead staining, cell attachment and proliferation assays indicating its potential as an effective treatment option for tissue regeneration in rotator cuff injuries or other tissues undergoing tensile biomechanical loading.

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ID Code: 241827
Item Type: Contribution to Journal (Journal Article)
Refereed: Yes
ORCID iD:
Mathew, Ashaorcid.org/0000-0002-8782-1981
Paxton, Naomi C.orcid.org/0000-0003-3052-4764
Woodruff, Maria A.orcid.org/0000-0002-4909-5288
Measurements or Duration: 10 pages
Keywords: drug encapsulation and release, melt electrowriting, PCL, vancomycin
DOI: 10.1002/mame.202300168
ISSN: 1438-7492
Pure ID: 140679205
Divisions: Current > Research Centres > Centre for Biomedical Technologies
Current > QUT Faculties and Divisions > Faculty of Engineering
Current > Schools > School of Mechanical, Medical & Process Engineering
Funding Information: A.M. and B.L.D. contributed equally to this work. Advance Queensland funded this research, Advance Queensland Industry Research Fellowships AQIRF0532018 (A.M.) and AQIRF2020 (N.P), Konica Minolta (A.M.), Bionics Queensland (A.M.), MMPE ECR catalyst grant (A.M.). N.P. acknowledges support from the Knight Campus‐PeaceHealth Postdoctoral Fellowship Program. B.L.D. and D.P. acknowledge support from Queensland University of Technology Postgraduate Research Awards. The authors would like to thank Dr. Edmund I. Pickering for his valuable assistance with drafting the mechanical characterization (Experimental Section).
Copyright Owner: 2023 The Authors
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Deposited On: 25 Jul 2023 01:46
Last Modified: 26 Jul 2024 15:20