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Calcium-deficient hydroxyapatite-PLGA composites: mechanical and microstructural investigation
1Materials Research Laboratory, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Journal of Biomedical Materials Research
|July 6, 2000
Summary
This study explores calcium deficient hydroxyapatite (CDHAp) and poly(lactide-co-glycolide) (PLGA) composites. Mechanical properties vary with composition and hydrolysis temperature, linked to microstructural changes.
Area of Science:
- Biomaterials Science
- Materials Engineering
- Composite Materials
Background:
- Calcium deficient hydroxyapatite (CDHAp) and poly(lactide-co-glycolide) (PLGA) composites are promising for biomedical applications.
- Understanding their microstructural and mechanical properties is crucial for optimizing performance.
Purpose of the Study:
- To investigate the microstructural and mechanical properties of CDHAp-PLGA composites.
- To analyze the effect of composition and hydrolysis temperature on composite properties.
Main Methods:
- Composites were synthesized via hydrolysis of alpha-tricalcium phosphate (alpha-TCP) to CDHAp in alpha-TCP-PLGA-NaCl precomposites.
- Isothermal calorimetry and X-ray diffraction monitored hydrolysis.
- Scanning electron microscopy examined microstructural evolution.
Main Results:
- Composites with 80:10:10 wt% alpha-TCP-PLGA-NaCl at 37°C showed tensile strength of 13.3 MPa, flexural strength of 24.8 MPa, and Young's modulus of 2.8 GPa.
- Composites with 60:20:20 wt% showed higher flexural strength (36.1 MPa) and Young's modulus (5.5 GPa), with lower tensile strength (12.0 MPa).
- Mechanical properties varied significantly with both hydrolysis temperature and precomposite composition.
Conclusions:
- The mechanical properties of CDHAp-PLGA composites are strongly influenced by their final microstructure.
- Microstructure is governed by polymer morphology changes around its glass transition temperature and CDHAp formation during hydrolysis.
- Optimizing composition and hydrolysis conditions is key to tailoring the mechanical performance of these biomaterials.