Clinical translation of polycaprolactone-based tissue engineering scaffolds, fabricated via additive manufacturing: A review of their craniofacial applications
- PMID: 38823255
- DOI: 10.1016/j.bioadv.2024.213902
Clinical translation of polycaprolactone-based tissue engineering scaffolds, fabricated via additive manufacturing: A review of their craniofacial applications
Abstract
The craniofacial region is characterized by its intricate bony anatomy and exposure to heightened functional forces presenting a unique challenge for reconstruction. Additive manufacturing has revolutionized the creation of customized scaffolds with interconnected pores and biomimetic microarchitecture, offering precise adaptation to various craniofacial defects. Within this domain, medical-grade poly(ε-caprolactone) (PCL) has been extensively used for the fabrication of 3D printed scaffolds, specifically tailored for bone regeneration. Its adoption for load-bearing applications was driven mainly by its mechanical properties, adjustable biodegradation rates, and high biocompatibility. The present review aims to consolidating current insights into the clinical translation of PCL-based constructs designed for bone regeneration. It encompasses recent advances in enhancing the mechanical properties and augmenting biodegradation rates of PCL and PCL-based composite scaffolds. Moreover, it delves into various strategies improving cell proliferation and the osteogenic potential of PCL-based materials. These strategies provide insight into the refinement of scaffold microarchitecture, composition, and surface treatments or coatings, that include certain bioactive molecules such as growth factors, proteins, and ceramic nanoparticles. The review critically examines published data on the clinical applications of PCL scaffolds in both extraoral and intraoral craniofacial reconstructions. These applications include cranioplasty, nasal and orbital floor reconstruction, maxillofacial reconstruction, and intraoral bone regeneration. Patient demographics, surgical procedures, follow-up periods, complications and failures are thoroughly discussed. Although results from extraoral applications in the craniofacial region are encouraging, intraoral applications present a high frequency of complications and related failures. Moving forward, future studies should prioritize refining the clinical performance, particularly in the domain of intraoral applications, and providing comprehensive data on the long-term outcomes of PCL-based scaffolds in bone regeneration. Future perspective and limitations regarding the transition of such constructs from bench to bedside are also discussed.
Keywords: Biocompatibility; Bioresorbable PCL; Composite scaffolds; Craniofacial region; Osteogenic differentiation; Τissue engineering.
Copyright © 2024 Elsevier B.V. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: YVONI KIRMANIDOU reports financial support was provided by Hellenic Foundation for Research and Innovation. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Similar articles
-
Osteoregenerative Potential of 3D-Printed Poly ε-Caprolactone Tissue Scaffolds In Vitro Using Minimally Manipulative Expansion of Primary Human Bone Marrow Stem Cells.Int J Mol Sci. 2023 Mar 3;24(5):4940. doi: 10.3390/ijms24054940. Int J Mol Sci. 2023. PMID: 36902373 Free PMC article.
-
Selective laser sintering fabrication of nano-hydroxyapatite/poly-ε-caprolactone scaffolds for bone tissue engineering applications.Int J Nanomedicine. 2013;8:4197-213. doi: 10.2147/IJN.S50685. Epub 2013 Nov 1. Int J Nanomedicine. 2013. PMID: 24204147 Free PMC article.
-
Fabrication and mechanical characterization of 3D printed vertical uniform and gradient scaffolds for bone and osteochondral tissue engineering.Acta Biomater. 2019 May;90:37-48. doi: 10.1016/j.actbio.2019.03.041. Epub 2019 Mar 21. Acta Biomater. 2019. PMID: 30905862 Free PMC article.
-
Advances in additive manufacturing of polycaprolactone based scaffolds for bone regeneration.J Mater Chem B. 2023 Aug 9;11(31):7250-7279. doi: 10.1039/d2tb02052a. J Mater Chem B. 2023. PMID: 37249247 Review.
-
Polycaprolactone usage in additive manufacturing strategies for tissue engineering applications: A review.J Biomed Mater Res B Appl Biomater. 2022 Jun;110(6):1479-1503. doi: 10.1002/jbm.b.34997. Epub 2021 Dec 17. J Biomed Mater Res B Appl Biomater. 2022. PMID: 34918463 Review.
Cited by
-
Enhanced Osteogenic Differentiation of hMSCs Using BMP@ZIF-8-Loaded GelMA Nanocomposite Hydrogels with Controlled BMP-2 Release.ACS Omega. 2025 Mar 11;10(11):10826-10834. doi: 10.1021/acsomega.4c06577. eCollection 2025 Mar 25. ACS Omega. 2025. PMID: 40160775 Free PMC article.
-
Alveolar Ridge Preservation Using Three-Dimensional Root Replicas of Polycaprolactone: A Radiological and Histological Evaluation of a Case Report.Reports (MDPI). 2025 Jun 9;8(2):92. doi: 10.3390/reports8020092. Reports (MDPI). 2025. PMID: 40710883 Free PMC article.
-
Challenges and future perspectives in using mesenchymal stem cells for efficient bone fracture healing.Front Bioeng Biotechnol. 2025 May 30;13:1568914. doi: 10.3389/fbioe.2025.1568914. eCollection 2025. Front Bioeng Biotechnol. 2025. PMID: 40521093 Free PMC article. Review.
-
Innovative Biocompatible Blend Scaffold of Poly(hydroxybutyrate-co-hydroxyvalerate) and Poly(ε-caprolactone) for Bone Tissue Engineering: In Vitro and In Vivo Evaluation.Polymers (Basel). 2024 Oct 30;16(21):3054. doi: 10.3390/polym16213054. Polymers (Basel). 2024. PMID: 39518269 Free PMC article.
-
Osteoclast-like multinucleated giant cells reinforce polycaprolactone grafts.Front Immunol. 2025 May 21;16:1572238. doi: 10.3389/fimmu.2025.1572238. eCollection 2025. Front Immunol. 2025. PMID: 40469291 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources