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Biodegradable microfibrous, electrospunned hydroxyapatite nanoparticles/poly(glycerol sebacate)-co-poly(ε-caprolactone) nanocomposite scaffolds for tissue engineering applications

Soft tissue engineering has focused on green, solvent-free biopolymers with rubber-like characteristics. One of the well-known elastomeric polyesters is polyglycerol sebacate (PGS). The present investigation involves the synthesis of a novel biopolymer composed of PGS- co -poly(ε-caprolactone) (PCL)...

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Bibliographic Details
Published in:Polymer bulletin (Berlin, Germany) Germany), 2024-08, Vol.81 (13), p.11499-11515
Main Authors: Pourhoseyini, Tahere, Naeimi, Farid, Mehrazin, Mehdi, Madadi, Mozhdeh, Khonakdar, Hossein Ali
Format: Article
Language:English
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Summary:Soft tissue engineering has focused on green, solvent-free biopolymers with rubber-like characteristics. One of the well-known elastomeric polyesters is polyglycerol sebacate (PGS). The present investigation involves the synthesis of a novel biopolymer composed of PGS- co -poly(ε-caprolactone) (PCL) copolymer, alongside hydroxyapatite (HA) using bovine bone. These synthesized materials were utilized to build scaffolds using 18–22 kV electrospinning. By in situ polymerization, PGS- co -PCL/HA nanocomposites with 5% and 10% hydroxyapatite nanoparticles were developed. Various analysis such as FTIR, TGA, SEM, and DSC were utilized to examine the prepared samples. Introducing 10% HA to the PGS- co -PCL copolymer blends boosted nanocomposite mechanical strength by 300%. Meanwhile, PGS- co -PCL-based samples and their nanocomposites demonstrated promising biocompatibility and antibacterial characteristics. Biodegradability experiments revealed that at pH 7, PGS- co -PCL-HA10% was degraded by 45% within 30 days, whereas at pH 11, degradation accelerated to 65%. This study’s findings provide a novel approach for soft tissue engineers to construct effective scaffolds with great biocompatibility and enhanced mechanical properties by combining PGS with co -PCL and adding HA nanoparticles.
ISSN:0170-0839
1436-2449
DOI:10.1007/s00289-024-05235-8