{"title":"Synthesis of a bioactive and degradable 70Poly(50Lactic-co-50Glycoric acid)/30(60SiO2-40CaQ) composite with dual pore structure","authors":"Jeong-Cheol Lee, I. Song, Suk-Young Kim, S. Rhee","doi":"10.1109/BIBE.2015.7367699","DOIUrl":null,"url":null,"abstract":"The bioactive and degradable 70poly(50lactic-co-50glycoric acid)/30(60SiO2-40CaO) composite, which had a dual pore structure, was synthesized by a gas expansion method. The bioactive 60SiO2-40CaO powders were prepared through a sol-gel method from tetraethyl orthosilicate and calcium nitrate tetrahydrate under nitric acidic condition followed by the heat treatment at 900°C for 1 h. The 70poly(50lactic-co-50glycoric acid)/30(60SiO2-40CaO) composite was then synthesized by a solvent casting method using 1,1,3,3-hexafluoro-2-propanol as a solvent. The disk-shaped 70poly(50lactic-co-50glycoric acid)/30(60SiO2-40CaO) composite was loaded into the custom-made high-pressure gas chamber and then carbon dioxide gas was introduced until achieving a final pressure of 20 MPa. After 1 day of loading, the carbon dioxide gas was released rapidly. The samples were observed by FE-SEM, the phase was evaluated by X-ray diffractometer, and its bioactivity was assessed in simulated body fluid. As a result, double pore structure was developed in the poly(50lactic-co-50glycoric acid) matrix after releasing the carbon dioxide gas and 60SiO2-40CaO particles were observed to place randomly among the poly(50lactic-co-50glycoric acid) matrix. After soaking in simulated body fluid for 1 week, flake-like low crystalline hydroxyl carbonate apatite was formed on the surface of the composite. The practical implication of the results is that it has promising potential for use as a scaffold material for bone tissue engineering due to its bioactivity and degradability.","PeriodicalId":422807,"journal":{"name":"2015 IEEE 15th International Conference on Bioinformatics and Bioengineering (BIBE)","volume":"64 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2015-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2015 IEEE 15th International Conference on Bioinformatics and Bioengineering (BIBE)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/BIBE.2015.7367699","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The bioactive and degradable 70poly(50lactic-co-50glycoric acid)/30(60SiO2-40CaO) composite, which had a dual pore structure, was synthesized by a gas expansion method. The bioactive 60SiO2-40CaO powders were prepared through a sol-gel method from tetraethyl orthosilicate and calcium nitrate tetrahydrate under nitric acidic condition followed by the heat treatment at 900°C for 1 h. The 70poly(50lactic-co-50glycoric acid)/30(60SiO2-40CaO) composite was then synthesized by a solvent casting method using 1,1,3,3-hexafluoro-2-propanol as a solvent. The disk-shaped 70poly(50lactic-co-50glycoric acid)/30(60SiO2-40CaO) composite was loaded into the custom-made high-pressure gas chamber and then carbon dioxide gas was introduced until achieving a final pressure of 20 MPa. After 1 day of loading, the carbon dioxide gas was released rapidly. The samples were observed by FE-SEM, the phase was evaluated by X-ray diffractometer, and its bioactivity was assessed in simulated body fluid. As a result, double pore structure was developed in the poly(50lactic-co-50glycoric acid) matrix after releasing the carbon dioxide gas and 60SiO2-40CaO particles were observed to place randomly among the poly(50lactic-co-50glycoric acid) matrix. After soaking in simulated body fluid for 1 week, flake-like low crystalline hydroxyl carbonate apatite was formed on the surface of the composite. The practical implication of the results is that it has promising potential for use as a scaffold material for bone tissue engineering due to its bioactivity and degradability.