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This study aims to establish a facile protocol for the preparation of a bi-layered poly(glycerol-sebacate) (PGS)/β-tricalcium phosphate (β-TCP) construct and to investigate its potential for bone-soft tissue engineering applications. The layered structure was prepared by distributing the ceramic particles within a prepolymer synthesized in a microwave reactor followed by a cross-linking of the final construct in vacuum (<10mbar). The vacuum stage led to the separation of cross-linked elastomer (top) and ceramic (bottom) phases. Results showed that addition of β-TCP particles to the elastomer matrix after the polymerization led to an increase in compression strength (up to 14±2.3MPa). Tensile strength (σ), Young's modulus (E), and elongation at break (

作者:Atakan, Tevlek;Pezhman, Hosseinian;Cansel, Ogutcu;Mustafa, Turk;Halil Murat, Aydin

来源:Materials science & engineering. C, Materials for biological applications 2017 年 72卷

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作者:
Atakan, Tevlek;Pezhman, Hosseinian;Cansel, Ogutcu;Mustafa, Turk;Halil Murat, Aydin
来源:
Materials science & engineering. C, Materials for biological applications 2017 年 72卷
标签:
Bi-layered Guided bone regeneration (GBR) Poly(glycerol-sebacate) Tissue engineering β-tricalcium phosphate
This study aims to establish a facile protocol for the preparation of a bi-layered poly(glycerol-sebacate) (PGS)/β-tricalcium phosphate (β-TCP) construct and to investigate its potential for bone-soft tissue engineering applications. The layered structure was prepared by distributing the ceramic particles within a prepolymer synthesized in a microwave reactor followed by a cross-linking of the final construct in vacuum (<10mbar). The vacuum stage led to the separation of cross-linked elastomer (top) and ceramic (bottom) phases. Results showed that addition of β-TCP particles to the elastomer matrix after the polymerization led to an increase in compression strength (up to 14±2.3MPa). Tensile strength (σ), Young's modulus (E), and elongation at break (