4.6 Article

Green synthesis and characterization of poly(glycerol-azelaic acid) and its nanocomposites for applications in regenerative medicine

Journal

JOURNAL OF APPLIED POLYMER SCIENCE
Volume 138, Issue 24, Pages -

Publisher

WILEY
DOI: 10.1002/app.50563

Keywords

biopolymers and renewable polymers; biosynthesis of polymers; biosynthesis of polymers

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A series of novel bio-polyester nanocomposites incorporating hydroxyapatite (HA) nanoparticles were prepared via in situ polymerization method, demonstrating good dispersibility and viscoelastic properties. The nanocomposites exhibited different thermal and degradation behaviors compared to the pristine sample. The presence of HA nanoparticles significantly influenced the hydrolytic degradation and cell attachment properties of the materials.
A series of novel bio-polyester nanocomposites based on glycerin and azelaic acid as monomers incorporating hydroxyapatite (HA) nanoparticles were fabricated via in situ polymerization method. Chemical structure of the samples was investigated by H-1-NMR, C-13-NMR, and Fourier-transform infrared spectroscopy (FTIR). Energy dispersive X-ray-mapping analysis illustrated that the nanoparticles were well dispersed in the poly (glycerol azelaic acid) (PGAZ) matrix. Viscoelastic properties of the samples under various frequencies were examined in which the PGAZ specimen containing 1.0 wt% of HA nanoparticles (PGAZH1.0) exhibited superlative properties. Furthermore, the alterations in the glass transition temperature of the samples were comprehensively discussed. Thermal gravimetric analysis displayed that nanocomposites generally have a difference in degradation patterns from that of the pristine sample. Dynamic contact angle demonstrated that the presence of HA nanoparticles imposed a significant influence on hydrophilicity. The hydrolytic degradation values at pH = 7 and pH = 11 were measured and determined that the degradation rate for the PGAZ sample containing 1.5 wt% HA (PGAZH1.5) was higher than those of the other samples. Moreover, in vitro studies elucidated that cell attachment on PGAZH1.0 and PAZH1.5 surfaces were acceptable.

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