Optimizing mandibular bone defect reconstruction using adipose-derived stem cells on 3-dimensionally printed polycaprolactone/xenograft scaffolds in canine model.
Mahdigholi N., Khojasteh A., Aminianfar H., Masoudifard M., Jabbarifakhr M., Nokhbatolfoghahaei H.
Animal Study on Face & Skin, published in BMC Oral Health (2025) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Animal Study
- Journal
- BMC Oral Health (2025)
- Country
- England
- Reported sample size
- —
- Source database
- PubMed
- PMID
- 41456036
- PMCID
- PMC12860160
- DOI
- 10.1186/s12903-025-07571-1
Abstract (original English)
Background Mandibular bone defects present significant challenges in reconstructive surgery due to their complex structure, and the body's limited ability to heal these areas naturally. Tissue engineering provides a promising solution, combined with stem cell therapy to overcome these obstacles. This study investigated the effects of adipose-derived mesenchymal stem cells (ADSCs) cultured on novel three-dimensional (3D)-printed polycaprolactone/xenograft scaffolds on the reconstruction and regeneration of segmental mandibular bone defects in canine models. Methods 3D-printed personalized PCL/xenograft scaffolds were designed and fabricated. After isolation and cultivation of canine ADSCs from their falciform tissues, they were seeded on 3D-printed scaffolds sterilized by gamma ray and implanted on 20 mm unilateral segmental mandibular bone defects of three dogs as the experimental group. Another three dogs received untreated scaffolds for their segmental defects. The defects were fixed with titanium plates. At 20 weeks post-implantation, the animals were sacrificed, the samples were harvested from all animals of both groups and three-dimensional microcomputed tomography (MicroCT), histopathological and immunohistochemistry analyses were performed. The parameters assessed included bone volume fraction, trabecular separation, trabecular number, trabecular thickness, new bone form
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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