The effect of hydroxyapatite filler on biodegradable poly(sorbitol sebacate malate) composites

Biodegradable poly(sorbitol sebacate malate)/hydroxyapatite (PSSM/HA) composites were successfully synthesized through one step catalyst‐free polycondensation of sorbitol, sebacic acid, malic acid, and HA powder as filler for the composites. The addition of HA improved the tensile modulus and streng...

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Veröffentlicht in:Journal of applied polymer science 2022-09, Vol.139 (36), p.n/a
Hauptverfasser: Yusoff, Noor Izyan Syazana Mohd, Tham, Weng Hong, Wahit, Mat Uzir, Abdul Kadir, Mohammed Rafiq, Wong, Tuck‐Whye
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Sprache:eng
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Zusammenfassung:Biodegradable poly(sorbitol sebacate malate)/hydroxyapatite (PSSM/HA) composites were successfully synthesized through one step catalyst‐free polycondensation of sorbitol, sebacic acid, malic acid, and HA powder as filler for the composites. The addition of HA improved the tensile modulus and strength of the materials compared with pure PSSM. The elongation at break of the composites was slightly reduced with increasing HA content. The PSSM and HA showed good compatibility, which was evidenced by good distributions of HA particles in the matrix. In vitro degradation and cytotoxicity tests were conducted to investigate the degradation profile and the toxicity of the biocomposites, respectively. The biocomposites also degraded nearly up to ~50% after 6 weeks of study and the degradation products were shown non‐cytotoxic. It was observed that the biocomposites were soft, elastic with Young's modulus and also biodegradable which is potential to be used in biomedical fields such as tissue engineering application. A family of thermoset biodegradable polyol‐based polyesters was successfully synthesized by catalyst‐free polycondensation of sorbitol, sebacic acid, and malic acid in the presence of HA. The composites were found to exhibit characteristics similar to that of elastomers and stiff thermosets. The effect of different HA loading on the properties of the polyesters composites were studied.
ISSN:0021-8995
1097-4628
DOI:10.1002/app.52862