Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Scientific Reports
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. scientific reports
  3. articles
  4. article
Calcium-enriched mesoporous silica/PLGA scaffolds enhance bone repair in a rabbit femoral condylar defect model
Download PDF
Download PDF
  • Article
  • Open access
  • Published: 17 March 2026

Calcium-enriched mesoporous silica/PLGA scaffolds enhance bone repair in a rabbit femoral condylar defect model

  • Honghan Wu1 na1,
  • Junxi Wu3 na1,
  • Hao Tang1 na1,
  • Qian Zhong1,
  • Guangquan Zhao1,
  • Qianyu Xie1,
  • Weikang Xu2 &
  • …
  • Qingde Wa1 

Scientific Reports , Article number:  (2026) Cite this article

  • 546 Accesses

  • Metrics details

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biotechnology
  • Materials science
  • Medical research
  • Stem cells

Abstract

Bone defects resulting from trauma, tumors, or infection continue to pose significant clinical challenges, particularly when the defect size exceeds the capacity for spontaneous healing. In this study, we fabricated two types of composite scaffolds—calcium carbonate/mesoporous silica/poly(lactic-co-glycolic acid) (CMP) and mesoporous silica/poly(lactic-co-glycolic acid) (MP)—using a single-emulsion solvent evaporation method. Both scaffolds exhibited interconnected porous structures and favorable morphology. In vitro assays demonstrated that CMP scaffolds more effectively promoted the proliferation and osteogenic differentiation of mesenchymal stem cells (MSCs) compared to MP scaffolds. Furthermore, a rabbit femoral condylar defect model was established to assess the in vivo bone regeneration efficacy and biocompatibility. Micro-CT imaging, along with hematoxylin-eosin (HE), Masson’s trichrome, and Movat’s pentachrome staining, as well as serum biochemical analyses, consistently indicated that CMP scaffolds significantly enhanced new bone formation and defect repair relative to MP scaffolds. Both scaffold types showed excellent tissue compatibility and elicited no adverse systemic effects. These findings suggest that calcium-enriched mesoporous silica/PLGA scaffolds hold strong potential as clinical biomaterials for the treatment of bone defects.

Similar content being viewed by others

3D-printed core–shell scaffolds with a biphasic calcium phosphate core and GelMA hydrogel shell for bone tissue engineering

Article Open access 28 February 2026

Multiple channels with interconnected pores in a bioceramic scaffold promote bone tissue formation

Article Open access 14 October 2021

Transcriptomic and cellular decoding of scaffolds-induced suture mesenchyme regeneration

Article Open access 23 April 2024

Data availability

All data generated or analyzed during this study are include in this published article.

References

  1. Qi, J. et al. Development and characterization of cannabidiol-loaded alginate copper hydrogel for repairing open bone defects in vitro[J]. Colloids Surf. B Biointerfaces. 212, 112339 (2022).

    Google Scholar 

  2. Yang, J. et al. Flavonoid-Loaded Biomaterials in Bone Defect Repair. Molecules, 28(19), 6888 (2023).

  3. Liu, Y. et al. Application of dental pulp stem cells for bone regeneration[J]. Front. Med. (Lausanne). 11, 1339573 (2024).

    Google Scholar 

  4. Sadek, A. A. et al. Enhancement of critical-sized bone defect regeneration using UiO-66 nanomaterial in rabbit femurs[J]. BMC Vet. Res. 18 (1), 260 (2022).

    Google Scholar 

  5. Liu, F. et al. The potential therapeutic role of extracellular vesicles in critical-size bone defects: Spring of cell-free regenerative medicine is coming[J]. Front. Bioeng. Biotechnol. 11, 1050916 (2023).

    Google Scholar 

  6. Aldaadaa, A., Owji, N. & Knowles, J. Three-dimensional Printing in Maxillofacial Surgery: Hype versus Reality[J]. J. Tissue Eng. 9, 1544466979 (2018).

    Google Scholar 

  7. Wang, Z. & Yang, Y. Application of 3D Printing in Implantable Medical Devices[J]. Biomed. Res. Int., 2021:6653967. (2021).

  8. Zhang, Y. et al. Bilayer Membrane Composed of Mineralized Collagen and Chitosan Cast Film Coated With Berberine-Loaded PCL/PVP Electrospun Nanofiber Promotes Bone Regeneration[J]. Front. Bioeng. Biotechnol. 9, 684335 (2021).

    Google Scholar 

  9. Xu, W. et al. Biodegradable calcium carbonate/mesoporous silica/poly(lactic-glycolic acid) microspheres scaffolds with osteogenesis ability for bone regeneration[J]. RSC Adv. 11 (9), 5055–5064 (2021).

    Google Scholar 

  10. Xu, W. et al. Storage and release of rare earth elements in microsphere-based scaffolds for enhancing osteogenesis[J]. Sci. Rep. 12 (1), 6383 (2022).

    Google Scholar 

  11. Song, R. et al. Current development of biodegradable polymeric materials for biomedical applications[J]. Drug Des. Devel Ther. 12, 3117–3145 (2018).

    Google Scholar 

  12. Shiroud Heidari, B. et al. Natural, synthetic and commercially-available biopolymers used to regenerate tendons and ligaments[J]. Bioact Mater. 19, 179–197 (2023).

    Google Scholar 

  13. Lin, Z. et al. Precisely controlled delivery of magnesium ions thru sponge-like monodisperse PLGA/nano-MgO-alginate core-shell microsphere device to enable in-situ bone regeneration[J]. Biomaterials 174, 1–16 (2018).

    Google Scholar 

  14. Bittner-Frank, M. et al. Cortical and trabecular mechanical properties in the femoral neck vary differently with changes in bone mineral density[J]. JBMR Plus. 8 (6), e49 (2024).

    Google Scholar 

  15. Smith, A. N. et al. Characterization of degradation kinetics of additively manufactured PLGA under variable mechanical loading paradigms[J]. J. Mech. Behav. Biomed. Mater. 153, 106457 (2024).

    Google Scholar 

  16. Xu, D. et al. Improvement of the mechanical properties and osteogenic activity of 3D-printed polylactic acid porous scaffolds by nano-hydroxyapatite and nano-magnesium oxide[J]. Heliyon 8 (6), e9748 (2022).

    Google Scholar 

  17. Owji, N. et al. Inclusion of calcium phosphate does not further improve in vitro and in vivo osteogenesis in a novel, highly biocompatible, mechanically stable and 3D printable polymer[J]. Sci. Rep. 12 (1), 16977 (2022).

    Google Scholar 

  18. Zhao, D. et al. Poly(lactic-co-glycolic acid)-based composite bone-substitute materials[J]. Bioactive Mater. 6 (2), 346–360 (2021).

    Google Scholar 

  19. Shen, M. et al. bFGF-Loaded Mesoporous Silica Nanoparticles Promote Bone Regeneration Through the Wnt/beta-Catenin Signalling Pathway[J]. Int. J. Nanomed. 17, 2593–2608 (2022).

    Google Scholar 

  20. Gong, S. et al. pH-Responsive Mesoporous Silica Nanoparticles Loaded with Naringin for Targeted Osteoclast Inhibition and Bone Regeneration[J]. Int. J. Nanomed. 19, 6337–6358 (2024).

    Google Scholar 

  21. Liang, W. et al. Current status of nano-embedded growth factors and stem cells delivery to bone for targeted repair and regeneration[J]. J. Orthop. Translat. 50, 257–273 (2025).

    Google Scholar 

  22. Budiman, A. et al. The Application of Mesoporous Silica Nanoparticles in Enhancing the Efficacy of Anti-Atherosclerosis Therapies: A Review[J]. Int. J. Nanomed. 20, 9825–9856 (2025).

    Google Scholar 

  23. Petousis, M. et al. Biomedical Composites of Polycaprolactone/Hydroxyapatite for Bioplotting: Comprehensive Interpretation of the Reinforcement Course[J]. Polym. (Basel), 16(17). (2024)

  24. Chen, Y. & Zhao, Q. Innovative modification strategies and emerging applications of natural hydrogel scaffolds for osteoporotic bone defect regeneration[J]. Front. Bioeng. Biotechnol. 13, 1591896 (2025).

    Google Scholar 

  25. Shi, X. et al. Novel mesoporous silica-based antibiotic releasing scaffold for bone repair[J]. Acta Biomater. 5 (5), 1697–1707 (2009).

    Google Scholar 

  26. Liu, H. et al. Unlocking the potential of amorphous calcium carbonate: A star ascending in the realm of biomedical application[J]. Acta Pharm. Sin B. 14 (2), 602–622 (2024).

    Google Scholar 

  27. Munyemana, J. C. et al. Recombinant Collagen-Templated Biomineralized Synthesis of Biocompatible pH-Responsive Porous Calcium Carbonate Nanospheres[J]. ACS Omega. 8 (34), 30879–30887 (2023).

    Google Scholar 

  28. Xiao, S. et al. In situ comparison of osteogenic effects of polymer-based scaffolds with different degradability by integrated scaffold model[J]. Colloids Surf. B Biointerfaces. 241, 114047 (2024).

    Google Scholar 

  29. Si, Y. et al. Curcumin-encapsulated exosomes in bisphosphonate-modified hydrogel microspheres promote bone repair through macrophage polarization and DNA damage mitigation[J]. Mater. Today Bio. 32, 101874 (2025).

    Google Scholar 

  30. Wang, G. et al. Surface Functionalization of Hydroxyapatite Scaffolds with MgAlEu-LDH Nanosheets for High-Performance Bone Regeneration[J]. Adv. Sci. (Weinh). 10 (1), e2204234 (2022).

    Google Scholar 

  31. Shineh, G. et al. Biomolecule-functionalized dental implant surfaces: Towards augmenting soft tissue integration[J]. Bioact Mater. 53, 540–590 (2025).

    Google Scholar 

  32. Chen, Q. et al. Promoting implant osseointegration via the osteoblast-selective beta-amino acid polymer strategy[J]. Nat. Commun. 16 (1), 7190 (2025).

    Google Scholar 

  33. Kuten Pella, O. et al. Albumin as a Biomaterial and Therapeutic Agent in Regenerative Medicine[J]. Int. J. Mol. Sci., 23(18). (2022)

  34. Shams, F. et al. A study on the cellular adhesion properties of a hybrid scaffold for vascular tissue engineering through molecular dynamics simulation[J]. Sci. Rep. 15 (1), 16433 (2025).

    Google Scholar 

  35. Moghaddam, A. S. et al. Hydrogels with multiple RGD presentations increase cell adhesion and spreading[J]. Acta Biomater. 199, 142–153 (2025).

    Google Scholar 

  36. Kim, J. et al. Effects of ECM protein mimetics on adhesion and proliferation of chorion derived mesenchymal stem cells[J]. Int. J. Med. Sci. 11 (3), 298–308 (2014).

    Google Scholar 

  37. Yan, B. et al. Surface modification progress for PLGA-based cell scaffolds. Polymers (Basel), 16(1), 165 (2024).

  38. de Carvalho, A. B. et al. Personalized bioceramic grafts for craniomaxillofacial bone regeneration[J]. Int. J. Oral Sci. 16 (1), 62 (2024).

    Google Scholar 

  39. Zhou, J. et al. Study on the influence of scaffold morphology and structure on osteogenic performance[J]. Front. Bioeng. Biotechnol. 11, 1127162 (2023).

    Google Scholar 

  40. Huang, D. et al. Biomimetic structural design in 3D-printed scaffolds for bone tissue engineering[J]. Mater. Today Bio. 32, 101664 (2025).

    Google Scholar 

  41. Aydin, M. S. et al. Impact of Porosity and Stiffness of 3D Printed Polycaprolactone Scaffolds on Osteogenic Differentiation of Human Mesenchymal Stromal Cells and Activation of Dendritic Cells[J]. ACS Biomater. Sci. Eng. 10 (12), 7539–7554 (2024).

    Google Scholar 

  42. Zebaze, R. et al. Increased Cortical Porosity and Reduced Trabecular Density Are Not Necessarily Synonymous With Bone Loss and Microstructural Deterioration[J]. JBMR Plus. 3 (4), e10078 (2019).

    Google Scholar 

  43. Coburn, B. & Salary, R. R. Mechanical characterization of porous bone-like scaffolds with complex microstructures for bone regeneration. Bioengineering (Basel), 12(4), 416 (2025).

  44. Zhang, B. et al. 3D-printed porous zinc scaffold combined with bioactive serum exosomes promotes bone defect repair in rabbit radius[J]. Aging (Albany NY). 16 (11), 9625–9648 (2024).

    Google Scholar 

  45. Matsushita, A. et al. Frequency-regulated repeated micro-vibration promotes osteoblast differentiation through BMP signaling in MC3T3-E1 cells. Life (Basel), 15(4), 588 (2025)

  46. Sun, Y., Jia, X. & Meng, Q. Characteristic Evaluation of Recombinant MiSp/Poly(lactic-co-glycolic) Acid (PLGA) Nanofiber Scaffolds as Potential Scaffolds for Bone Tissue Engineering[J]. Int. J. Mol. Sci., 24(2). (2023).

  47. Contreras-Caceres, R. et al. Electrospun nanofibers: Recent applications in drug delivery and cancer therapy. Nanomaterials (Basel), 9(4), 656 (2019)

  48. Lian, M. et al. Bi-layered electrospun nanofibrous membrane with osteogenic and antibacterial properties for guided bone regeneration[J]. Colloids Surf. B Biointerfaces. 176, 219–229 (2019).

    Google Scholar 

  49. Gentili, C. et al. Sustainably cultured coral scaffold supports human bone marrow mesenchymal stromal cell osteogenesis[J]. Regen Ther. 26, 366–381 (2024).

    Google Scholar 

  50. Lun, D. et al. Limitations and modifications in the clinical application of calcium sulfate[J]. Front. Surg. 11, 1278421 (2024).

    Google Scholar 

  51. Viti, F. et al. Osteogenic Differentiation of MSC through Calcium Signaling Activation: Transcriptomics and Functional Analysis[J]. PloS one. 11 (2), e148173 (2016).

    Google Scholar 

  52. Cheng, L. et al. Black phosphorus-based 2D materials for bone therapy[J]. Bioactive Mater. 5 (4), 1026–1043 (2020).

    Google Scholar 

  53. Liu, T. et al. Customized Design 3D Printed PLGA/Calcium Sulfate Scaffold Enhances Mechanical and Biological Properties for Bone Regeneration[J]. Front. Bioeng. Biotechnol. 10, 874931 (2022).

    Google Scholar 

  54. Chen, X. et al. Mesoporous silica promotes osteogenesis of human adipose-derived stem cells identified by a high-throughput microfluidic chip assay. Pharmaceutics, 14(12), 2730 (2022)

  55. Nii, T. & Katayama, Y. Biomaterial-assisted regenerative medicine. Int. J. Mol. Sci., 22(16), 8657 (2021).

  56. Min, K. H. et al. Biomimetic scaffolds of calcium-based materials for bone regeneration. Biomimetics (Basel), 9(9), 511 (2024)

Download references

Funding

This study was supported by The National Natural Science Foundation of China (82160577); The Zunyi City Science & Technology Innovation Talent Project (No. [2024] 04).

Author information

Author notes
  1. These authors contributed equally to this work: Honghan Wu, Junxi Wu and Hao Tang.

Authors and Affiliations

  1. Departament of Orthopadic Surgery, The Second Affiliate Hospital of Zunyi Medical University, Zunyi, 563000, China

    Honghan Wu, Hao Tang, Qian Zhong, Guangquan Zhao, Qianyu Xie & Qingde Wa

  2. Institute of Biological and Medical Engineering, Guangdong Academy of Sciences, Guangzhou, 510632, China

    Weikang Xu

  3. Zunyi Medical University, Zunyi, 563000, China

    Junxi Wu

Authors
  1. Honghan Wu
    View author publications

    Search author on:PubMed Google Scholar

  2. Junxi Wu
    View author publications

    Search author on:PubMed Google Scholar

  3. Hao Tang
    View author publications

    Search author on:PubMed Google Scholar

  4. Qian Zhong
    View author publications

    Search author on:PubMed Google Scholar

  5. Guangquan Zhao
    View author publications

    Search author on:PubMed Google Scholar

  6. Qianyu Xie
    View author publications

    Search author on:PubMed Google Scholar

  7. Weikang Xu
    View author publications

    Search author on:PubMed Google Scholar

  8. Qingde Wa
    View author publications

    Search author on:PubMed Google Scholar

Contributions

**Honghan Wu: ** Writing–original draft, Software, Methodology, Investigation.**Junxi Wu: ** Resources, Methodology, Formal analysis. **Hao Tang: ** Validation, Methodology. **Qian Zhong: ** Visualization, Data curation. **Guangquan Zhao: ** Visualization, Conceptualization. **Qianyu Xie: ** Software, Validation. **Weikang Xu: ** review & editing. **Qingde Wa: ** Writing - review & editing, Funding acquisition, Supervision, Conceptualization.

Corresponding authors

Correspondence to Weikang Xu or Qingde Wa.

Ethics declarations

Competing interests

The authors declare no competing interests.

Ethics approval

All experimental protocols of this study have been approved by the Medical Ethics Committee of Zunyi Medical University, and all methods were carried out in accordance with ARRIVE guidelines and regulations (the anesthesia method used in this study was intramuscular injection of xylazine hydrochloride).

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wu, H., Wu, J., Tang, H. et al. Calcium-enriched mesoporous silica/PLGA scaffolds enhance bone repair in a rabbit femoral condylar defect model. Sci Rep (2026). https://doi.org/10.1038/s41598-026-44490-9

Download citation

  • Received: 16 September 2025

  • Accepted: 11 March 2026

  • Published: 17 March 2026

  • DOI: https://doi.org/10.1038/s41598-026-44490-9

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Keywords

  • Bone defect repair
  • In vivo evaluation
  • Calcium-enriched mesoporous silica/PLGA
  • Rabbit femoral defect model
  • Histological and micro-CT analysis
Download PDF

Associated content

Collection

Functional polymers

Advertisement

Explore content

  • Research articles
  • News & Comment
  • Collections
  • Subjects
  • Follow us on Facebook
  • Follow us on X
  • Sign up for alerts
  • RSS feed

About the journal

  • About Scientific Reports
  • Contact
  • Journal policies
  • Guide to referees
  • Calls for Papers
  • Editor's Choice
  • Journal highlights
  • Open Access Fees and Funding

Publish with us

  • For authors
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Scientific Reports (Sci Rep)

ISSN 2045-2322 (online)

nature.com footer links

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2026 Springer Nature Limited

Nature Briefing: Translational Research

Sign up for the Nature Briefing: Translational Research newsletter — top stories in biotechnology, drug discovery and pharma.

Get what matters in translational research, free to your inbox weekly. Sign up for Nature Briefing: Translational Research