通过原位聚合法制备新型生物活性羟基磷灰石/二元氨基酸共聚物(BHA/PAA)复合材料。采用1 H核磁共振(1 H NMR)、红外光谱(IR)、X-ray衍射光谱(XRD)、X射线光电子能谱(XPS)、扫描电镜(SEM)和差示扫描量热分析(DSC)对其组成结构、热性能、...通过原位聚合法制备新型生物活性羟基磷灰石/二元氨基酸共聚物(BHA/PAA)复合材料。采用1 H核磁共振(1 H NMR)、红外光谱(IR)、X-ray衍射光谱(XRD)、X射线光电子能谱(XPS)、扫描电镜(SEM)和差示扫描量热分析(DSC)对其组成结构、热性能、力学性能和体外降解性能进行研究。结果表明:BHA颗粒均匀分散在PAA基质中,形成的复合材料具有良好的均一性;复合材料的无机相和有机相之间存在着一定的化学键相互作用;由于BHA的引入,复合材料的结晶速率加快,整体结晶度下降;复合材料具有良好的力学性能,其抗压强度随着BHA含量的增加而明显提高,抗弯强度略有减小,当BHA含量为30%(质量分数)时,复合材料的抗压强度和抗弯强度分别为141.02MPa和86.32MPa,力学性能与人体皮质骨相匹配;体外降解实验结果表明,随着BHA含量的增加,材料的降解速率加快,且在降解过程中保持良好的力学性能稳定性,在骨修复方面具有潜在的应用。展开更多
Polypeptide graft copolymers such as poly(γ-benzyl-L-glutamate)(PBLG)-poly(ethylene glycol)(PEG) and poly(γ-ethyl-L-glutamate)(PELG)-poly(ethylene glycol)(PEG) were introduced into self-setting calcium phosphate cem...Polypeptide graft copolymers such as poly(γ-benzyl-L-glutamate)(PBLG)-poly(ethylene glycol)(PEG) and poly(γ-ethyl-L-glutamate)(PELG)-poly(ethylene glycol)(PEG) were introduced into self-setting calcium phosphate cement(CPC) system to improve its mechanical properties. The compression strength was improved considerably by the induction of polypeptide copolymers. It is about 22.3 higher for PBLG-g-PEG and 65.0 higher for PELG-g-PEG, respectively. The results also show that for the same polypeptide copolymer, higher compression strength of composites can be obtained by introducing copolymer micelles into the CPC. According to the results of scanning electron microscope(SEM), the crystallite shapes of CPC depend on the weight fraction of polypeptide copolymer in the composites.展开更多
文摘通过原位聚合法制备新型生物活性羟基磷灰石/二元氨基酸共聚物(BHA/PAA)复合材料。采用1 H核磁共振(1 H NMR)、红外光谱(IR)、X-ray衍射光谱(XRD)、X射线光电子能谱(XPS)、扫描电镜(SEM)和差示扫描量热分析(DSC)对其组成结构、热性能、力学性能和体外降解性能进行研究。结果表明:BHA颗粒均匀分散在PAA基质中,形成的复合材料具有良好的均一性;复合材料的无机相和有机相之间存在着一定的化学键相互作用;由于BHA的引入,复合材料的结晶速率加快,整体结晶度下降;复合材料具有良好的力学性能,其抗压强度随着BHA含量的增加而明显提高,抗弯强度略有减小,当BHA含量为30%(质量分数)时,复合材料的抗压强度和抗弯强度分别为141.02MPa和86.32MPa,力学性能与人体皮质骨相匹配;体外降解实验结果表明,随着BHA含量的增加,材料的降解速率加快,且在降解过程中保持良好的力学性能稳定性,在骨修复方面具有潜在的应用。
文摘Polypeptide graft copolymers such as poly(γ-benzyl-L-glutamate)(PBLG)-poly(ethylene glycol)(PEG) and poly(γ-ethyl-L-glutamate)(PELG)-poly(ethylene glycol)(PEG) were introduced into self-setting calcium phosphate cement(CPC) system to improve its mechanical properties. The compression strength was improved considerably by the induction of polypeptide copolymers. It is about 22.3 higher for PBLG-g-PEG and 65.0 higher for PELG-g-PEG, respectively. The results also show that for the same polypeptide copolymer, higher compression strength of composites can be obtained by introducing copolymer micelles into the CPC. According to the results of scanning electron microscope(SEM), the crystallite shapes of CPC depend on the weight fraction of polypeptide copolymer in the composites.
