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首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >In vitro degradation behavior of a hydroxyapatite/poly(lactide-co-glycolide) composite reinforced by micro/nano-hybrid poly(glycolide) fibers for bone repair
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In vitro degradation behavior of a hydroxyapatite/poly(lactide-co-glycolide) composite reinforced by micro/nano-hybrid poly(glycolide) fibers for bone repair

机译:通过微/纳米杂交聚(乙酰胺)纤维加强羟基磷灰石/聚(丙交酯 - 共乙酰基)复合物的体外降解行为,用于骨修复

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摘要

A poly(glycolide) (PGA) fiber-reinforced hydroxyapatite/poly(lactide-co-glycolide) (HA/PLGA) composite with high mechanical strength has been prepared previously. In this paper, in vitro degradation of ternary composites with different contents of PGA fibers (0, 30, 50 and 70 wt%) was investigated. Water absorption showed a marked increase as the degradation progressed, and the composite with 70 wt% PGA fibers showed the highest final water uptake which was 3.89 times higher than the initial value. The mass loss of the composite with 70 wt% PGA fibers was 79.3 +/- 6.47% at 16 weeks, which was the highest among all the composites. The molecular weight of the PLGA matrix decreased over time especially for the composites containing 70 wt% PGA fibers. The lowest pH of the buffer solution was also observed in the composite with 70 wt% PGA fibers. Environmental scanning electron microscopy (ESEM) and micro-computed tomography (micro-CT) results demonstrated that the porosity of the composites and the size of the pores gradually increased as the degradation progressed. The most significant change in compression strength was observed for the composite with 70 wt% PGA fibers which was reduced from an initial value of 20 MPa to approximately 1 MPa at 16 weeks. The results indicated that the in vitro degradation of the composites could be accelerated by increasing the content of PGA fibers. It implied that the ternary composites might be a candidate for the repair of non-load bearing or cancellous bone which needs high initial strength and fast degradation rate.
机译:以前制备了聚(乙酰基)(PGA)纤维增强羟基磷灰石/聚(丙交酯 - 共乙酰胺)(HA / PLGGA)复合材料,具有高机械强度。本文研究了研究具有不同含量的PGA纤维(0,30,50和70wt%)的三元复合材料的体外降解。吸水率显示出显着的增加随着降解的进展,具有70wt%PGA纤维的复合材料显示出最终的最终水吸收,其比初始值高3.89倍。在16周的16周内,70wt%PGA纤维的复合材料的质量损失为79.3 +/- 6.47%,这是所有复合材料中最高的。 PLGA基质的分子量随着时间的推移而降低,特别是对于含有70wt%PGA纤维的复合材料。在具有70wt%PGA纤维的复合材料中也观察到缓冲溶液的最低pH。环境扫描电子显微镜(ESEM)和微计算断层扫描(Micro-CT)结果表明,随着降解进展,复合材料的孔隙率和孔的尺寸逐渐增加。对于具有70wt%PGA纤维的复合材料,观察到压缩强度最显着的变化,其在16周的初始值为20MPa至约1MPa。结果表明,通过增加PGA纤维的含量,可以加速复合材料的体外降解。它暗示三元复合材料可能是修复不承载或松质骨骼的候选者,这需要高初始强度和快速降解率。

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    Chinese Acad Sci Changchun Inst Appl Chem Key Lab Polymer Ecomat 5625 Renmin St Changchun 130022 Jilin Peoples R China;

    Chinese Acad Sci Changchun Inst Appl Chem Key Lab Polymer Ecomat 5625 Renmin St Changchun 130022 Jilin Peoples R China;

    Chinese Acad Sci Changchun Inst Appl Chem Key Lab Polymer Ecomat 5625 Renmin St Changchun 130022 Jilin Peoples R China;

    Chinese Acad Sci Changchun Inst Appl Chem Key Lab Polymer Ecomat 5625 Renmin St Changchun 130022 Jilin Peoples R China;

    Chinese Acad Sci Changchun Inst Appl Chem Key Lab Polymer Ecomat 5625 Renmin St Changchun 130022 Jilin Peoples R China;

    Jilin Univ China Japan Union Hosp Dept Orthoped 126 Xiantai St Changchun 130033 Jilin Peoples R China;

    Chinese Acad Sci Changchun Inst Appl Chem Key Lab Polymer Ecomat 5625 Renmin St Changchun 130022 Jilin Peoples R China;

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  • 正文语种 eng
  • 中图分类 分析化学;
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