3D-Printed Medical-Grade Polycaprolactone (mPCL) Scaffold for the Surgical Treatment of Vaginal Prolapse and Abdominal Hernias

Author:

Russo Serafini Mairim12ORCID,Mowat Alexandra34,Mustafa Susanah4,Saifzadeh Siamak25ORCID,Shabab Tara26,Bas Onur26,O’Rourke Nicholas7,W. Hutmacher Dietmar268ORCID,Medeiros Savi Flavia268ORCID

Affiliation:

1. Department of Pharmacy, Universidade Federal de Sergipe, São Cristóvão 49100-000, Brazil

2. Centre in Regenerative Medicine, Faculty of Engineering, Queensland University of Technology, Brisbane, QLD 4059, Australia

3. Faculty of Medicine, University of Queensland, Brisbane, QLD 4072, Australia

4. Queen Elisabeth II Jubilee Hospital, Brisbane, QLD 4108, Australia

5. Medical Engineering Research Facility, Queensland University of Technology, Brisbane, QLD 4032, Australia

6. Australian Research Council Industrial Transformation Training Centre in Additive Biomanufacturing, Queensland University of Technology, Brisbane, QLD 4059, Australia

7. Department of Hepato-Pancreato-Biliary Surgery, Royal Brisbane and Women’s Hospital, University of Queensland, Brisbane, QLD 4029, Australia

8. ARC Training Centre for Multiscale 3D Imaging, Modelling and Manufacturing, Brisbane, QLD 4059, Australia

Abstract

The expected outcome after a scaffold augmented hernia repair is the regeneration of a tissue composition strong enough to sustain biomechanical function over long periods. It is hypothesised that melt electrowriting (MEW) medical-grade polycaprolactone (mPCL) scaffolds loaded with platelet-rich plasma (PRP) will enhance soft tissue regeneration in fascial defects in abdominal and vaginal sheep models. A pre-clinical evaluation of vaginal and abdominal hernia reconstruction using mPCL mesh scaffolds and polypropylene (PP) meshes was undertaken using an ovine model. Each sheep was implanted with both a PP mesh (control group), and a mPCL mesh loaded with PRP (experimental group) in both abdominal and vaginal sites. Mechanical properties of the tissue-mesh complexes were assessed with plunger tests. Tissue responses to the implanted meshes were evaluated via histology, immunohistochemistry and histomorphometry. At 6 months post-surgery, the mPCL mesh was less stiff than the PP mesh, but stiffer than the native tissue, while showing equitable collagen and vascular ingrowth when compared to PP mesh. The results of this pilot study were supportive of mPCL as a safe and effective biodegradable scaffold for hernia and vaginal prolapse repair, hence a full-scale long-term study (over 24–36 months) with an adequate sample size is recommended.

Funder

RANZCOG scholarship

Publisher

MDPI AG

Subject

Bioengineering

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