Poly(caprolactone)‐aligned nanofibers associated with fibronectin‐loaded collagen hydrogel as a potent bioactive scaffold for cell‐free regenerative endodontics
Aim Guided tissue regeneration has been considered a promising strategy to replace conventional endodontic therapy of teeth with incomplete root formation. Therefore, the objective of this study was to develop a tubular scaffold (TB‐SC) with poly (caprolactone)‐aligned nanofibres associated with a f...
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Veröffentlicht in: | International endodontic journal 2022-12, Vol.55 (12), p.1359-1371 |
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Sprache: | eng |
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Zusammenfassung: | Aim
Guided tissue regeneration has been considered a promising strategy to replace conventional endodontic therapy of teeth with incomplete root formation. Therefore, the objective of this study was to develop a tubular scaffold (TB‐SC) with poly (caprolactone)‐aligned nanofibres associated with a fibronectin (FN)‐loaded collagen hydrogel and assess the pulp regeneration potential mediated by human apical papilla cells (hAPCs) using an in vitro model of teeth with incomplete root formation.
Methodology
Aligned nanofibre strips based on 10% poly(caprolactone) (PCL) were synthesized with the electrospinning technique to produce the TB‐SCs. These were submitted to different treatments, according to the following groups: TB‐SC (negative control): TB‐SC without treatment; TB‐SC + FN (positive control): TB‐SC coated with 10 μg/ml of FN; TB‐SC + H: TB‐SC associated with collagen hydrogel; TB‐SC + HFN: TB‐SC associated with FN‐loaded collagen hydrogel. Then, the biomaterials were inserted into cylindrical devices to mimic the regenerative therapy of teeth with incomplete root formation. The hAPCs were seeded on the upper surface of the TB‐SCs associated or not with any treatment, and cell migration/proliferation and the gene expression of markers related to pulp regeneration (ITGA5, ITGAV, COL1A1 and COL1A3) were evaluated. The data were submitted to anova/Tukey's tests (α = 5%).
Results
Higher values of cell migration/proliferation and gene expression of all markers tested were observed in groups TB‐SC + FN, TB‐SC + H, and TB‐SC + HFN compared with the TB‐SC group (p |
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ISSN: | 0143-2885 1365-2591 |
DOI: | 10.1111/iej.13823 |