journal article·2026-07-23

Polymer Composition Modulates Dental Stem Cell Response and Mineralization in Electrospun Scaffolds for Hard Tissue Regeneration

Caroline Anselmi, Sepideh Aminmansour, Igor Paulino Mendes Soares, Alexandre Henrique dos Reis-Prado, Sahar Aminmansour, Owen Liepman, Renan Dal-Fabbro, Josimeri Hebling, Marco C. Bottino

Biomimetics· Volume 11· Issue 8
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Abstract

Material selection is crucial to hard tissue regeneration, and matching scaffold properties to those of the target tissue can improve clinical outcomes. This study compared the physicochemical, mechanical, and biological performance of fibrous scaffolds fabricated from polycaprolactone (PCL), polydioxanone (PDO), and gelatin methacryloyl (GelMA) for hard tissue regeneration. Polymeric fibers were produced by electrospinning, and their morphological, physical, and mechanical properties were characterized by scanning electron microscopy (SEM, n = 2), swelling and degradation analyses (n = 8), water contact angle measurements (n = 16), and tensile testing (n = 8). In addition, periodontal ligament stem cells (PDLSCs), alveolar bone marrow stem cells (aBMSCs), and dental pulp stem cells (DPSCs) were seeded onto the scaffolds to evaluate cell spreading (n = 4), viability (n = 8), and mineralized matrix formation (n = 6). Data were analyzed using one- or two-way ANOVA followed by appropriate post hoc tests (α = 5%). All polymers formed homogeneous fibrous scaffolds, with diameters within the nanoscale range. PDO and GelMA showed higher swelling than PCL, while PCL retained approximately 95% of its initial mass after three months. PCL and PDO showed higher elongation at break, tensile strength, and Young’s modulus than GelMA. Both PDO and GelMA displayed contact angles below 90°, with GelMA showing the lowest values. In vitro, all polymers were cytocompatible: PDO and GelMA enhanced DPSC viability at 7 days, whereas GelMA produced the highest viability for PDLSCs and aBMSCs at that time point. GelMA also promoted the highest mineralized matrix formation for DPSCs and PDLSCs, with no significant differences among polymers for aBMSCs. Overall, GelMA scaffolds promoted greater cell viability and mineralized matrix formation, while PCL and PDO provided superior mechanical properties, highlighting the importance of balancing biological and mechanical requirements when designing scaffolds for hard tissue regeneration.
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Research context

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Affiliations

Department of Cariology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI 48109, USA

Department of Oral and Maxillofacial Diagnostic Sciences, College of Dentistry, University of Florida, Gainesville, FL 32610, USA

Department of Dental Materials and Prosthodontics, School of Dentistry, São Paulo State University (UNESP), Araraquara 14801-385, SP, Brazil

Department of Restorative Dentistry, School of Dentistry, Minas Gerais Federal University (UFMG), Belo Horizonte 31270-901, MG, Brazil

Department of Morphology and Pediatric Dentistry, School of Dentistry, São Paulo State University (UNESP), Araraquara 14801-385, SP, Brazil

Department of Biomedical Engineering, College of Engineering, University of Michigan, Ann Arbor, MI 48109, USA

Funding

National Institutes of Health

References (45)

Show source-provided references
1. Global Burden of Severe Tooth Loss: A Systematic Review and Meta-analysis10.1177/0022034514537828 ↗
2. The Interplay Between Periodontitis, Caries and Dental Restorations in an Adult Population10.1111/jcpe.70043 ↗
3. WHO’s global oral health status report 2022: Actions, discussion and implementation10.1111/odi.14516 ↗
4. Injectable scaffolds: Preparation and application in dental and craniofacial regeneration10.1016/j.mser.2016.11.001 ↗
5. Biomaterials-based strategy for dental-oral tissue regeneration: Current clinical application, laboratory development, and future direction10.1016/j.biomaterials.2025.123714 ↗
6. A review of the structural and physical properties that govern cell interactions with structured biomaterials enabled by additive manufacturing10.1016/j.bprint.2022.e00201 ↗
7. Abbass, M.M.S., El-Rashidy, A.A., Sadek, K.M., Moshy, S.E., Radwan, I.A., Rady, D., Dorfer, C.E., and Fawzy El-Sayed, K.M. (2020). Hydrogels and Dentin-Pulp Complex Regeneration: From the Benchtop to Clinical Translation. Polymers, 12.10.3390/polym12122935 ↗
8. Bilayer gelatin-methacryloyl scaffold for pulp inflammation suppression and dentin-like tissue regeneration10.1016/j.jconrel.2025.114469 ↗
9. Tissue-specific melt electrowritten polymeric scaffolds for coordinated regeneration of soft and hard periodontal tissues
10. Injectable Highly Tunable Oligomeric Collagen Matrices for Dental Tissue Regeneration10.1021/acsabm.9b00944 ↗
11. The role of mesenchymal stem cells-derived from oral and teeth in regenerative and reconstructive medicine10.1016/j.tice.2025.102766 ↗
12. Vasculogenic Precedes Neurogenic Differentiation in Dental Pulp Stem Cells10.1177/00220345251379776 ↗
13. Immunomodulatory properties of human periodontal ligament stem cells10.1002/jcp.21710 ↗
14. Bone regeneration capacities of alveolar bone mesenchymal stem cells sheet in rabbit calvarial bone defect10.1177/2041731420930379 ↗
15. Differences in osteogenic and odontogenic differentiation potential of DPSCs and SHED10.1016/j.jdent.2020.103413 ↗
16. Guidance for evaluating biomaterials’ properties and biological potential for dental pulp tissue engineering and regeneration research10.1016/j.dental.2024.12.003 ↗
17. Influence of Surface Chemistry on Adhesion and Osteo/Odontogenic Differentiation of Dental Pulp Stem Cells10.1021/acsbiomaterials.7b00274 ↗
18. Next-generation biomaterials for dental pulp tissue immunomodulation10.1016/j.dental.2023.03.013 ↗
19. Resorbable Membranes for Guided Bone Regeneration: Critical Features, Potentials, and Limitations10.1021/acsmaterialsau.3c00013 ↗
20. Designed hybrid scaffolds consisting of polycaprolactone microstrands and electrospun collagen-nanofibers for bone tissue regeneration10.1002/jbm.b.31809 ↗
21. Polycaprolactone (PCL): The biodegradable polyester shaping the future of materials—A review on synthesis, properties, biodegradation, applications and future perspectives10.1016/j.eurpolymj.2025.114033 ↗
22. 3D Printing beta-TCP-laden GelMA/Alginate Interpenetrating-Polymer-Network Biomaterial Inks for Bone Tissue Engineering10.1016/j.bprint.2025.e00413 ↗
23. Strategies of functionalized GelMA-based bioinks for bone regeneration: Recent advances and future perspectives
24. Yu, H., Luo, X., Li, Y., Shao, L., Yang, F., Pang, Q., Zhu, Y., and Hou, R. (2024). Advanced Hybrid Strategies of GelMA Composite Hydrogels in Bone Defect Repair. Polymers, 16.10.3390/polym16213039 ↗
25. Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties10.1016/j.dental.2024.06.019 ↗
26. Anti-inflammatory potential of casein enzymatic hydrolysate/gelatin methacryloyl scaffolds for vital pulp therapy10.1007/s00784-024-05877-y ↗
27. Ayoub, A.A., Mahmoud, A.H., Ribeiro, J.S., Daghrery, A., Xu, J., Fenno, J.C., Schwendeman, A., Sasaki, H., Dal-Fabbro, R., and Bottino, M.C. (2022). Electrospun Azithromycin-Laden Gelatin Methacryloyl Fibers for Endodontic Infection Control. Int. J. Mol. Sci., 23.10.3390/ijms232213761 ↗
28. Robles, K.N., Zahra, F.T., Mu, R., and Giorgio, T. (2024). Advances in Electrospun Poly(epsilon-caprolactone)-Based Nanofibrous Scaffolds for Tissue Engineering. Polymers, 16.10.3390/polym16202853 ↗
29. Polycaprolactone usage in additive manufacturing strategies for tissue engineering applications: A review10.1002/jbm.b.34997 ↗
30. Multifunctional GelMA platforms with nanomaterials for advanced tissue therapeutics
31. GelMA hydrogels reinforced by PCL@GelMA nanofibers and bioactive glass induce bone regeneration in critical size cranial defects10.1186/s12951-024-02980-w ↗
32. Zhuang, Y., Lin, K., and Yu, H. (2019). Advance of Nano-Composite Electrospun Fibers in Periodontal Regeneration. Front. Chem., 7.10.3389/fchem.2019.00495 ↗
33. Effect of wettability and surface functional groups on protein adsorption and cell adhesion using well-defined mixed self-assembled monolayers10.1016/j.biomaterials.2007.03.013 ↗
34. Nanofibrous GelMA-Based Scaffolds Support Human Adipose-Derived Mesenchymal Stem/Stromal Cell Adhesion, Viability, and Growth10.1002/jbm.a.37914 ↗
35. The effect of processing variables on the morphology of electrospun nanofibers and textiles10.1016/S0032-3861(00)00250-0 ↗
36. Electrospun PCL-Based Materials for Health-Care Applications: An Overview10.1002/mame.202300388 ↗
37. Collagen surface modified poly(ε-caprolactone) scaffolds with improved hydrophilicity and cell adhesion properties10.1016/j.matlet.2014.06.132 ↗
38. Nanofibers reinforced injectable hydrogel with self-healing, antibacterial, and hemostatic properties for chronic wound healing10.1016/j.jcis.2021.02.107 ↗
39. The normal stiffness of the edentulous alveolar process10.1016/j.bonr.2021.101066 ↗
40. Teixeira, M.O., Antunes, J.C., and Felgueiras, H.P. (2021). Recent Advances in Fiber-Hydrogel Composites for Wound Healing and Drug Delivery Systems. Antibiotics, 10.10.3390/antibiotics10030248 ↗
41. Sequentially-crosslinked biomimetic bioactive glass/gelatin methacryloyl composites hydrogels for bone regeneration10.1016/j.msec.2018.03.029 ↗
42. Aldana, A.A., Malatto, L., Rehman, M.A.U., Boccaccini, A.R., and Abraham, G.A. (2019). Fabrication of Gelatin Methacrylate (GelMA) Scaffolds with Nano- and Micro-Topographical and Morphological Features. Nanomaterials, 9.10.3390/nano9010120 ↗
43. Nanoscale beta-TCP-Laden GelMA/PCL Composite Membrane for Guided Bone Regeneration10.1021/acsami.3c03059 ↗
44. A Novel Strategy to Engineer Pre-Vascularized Full-Length Dental Pulp-like Tissue Constructs10.1038/s41598-017-02532-3 ↗
45. GelMA-Encapsulated hDPSCs and HUVECs for Dental Pulp Regeneration10.1177/0022034516682005 ↗