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丝素/磷酸钙/硫酸钙复合材料的制备及其性能研究

Studies on Preparation and Properties of Silk Fibroin/Calcium Phosphate/Calcium Sulfate Composites

【作者】 黄阳阳

【导师】 谢瑞娟;

【作者基本信息】 苏州大学 , 纺织材料与纺织品设计, 2012, 硕士

【摘要】 本文在合成磷酸钙骨水泥(CPC)、制备丝素(SF)微球的基础上,通过在CPC中添加以无定形结构为主的丝素微球(SFP)和半水硫酸钙(CSH)制备了可注射可原位固化成孔的SFP/CPC/CSH复合材料,研究SFP比例、CSH比例和液固比对材料的结构、性能的影响,并调查样品在模拟体液(SBF)中结构和性能的变化,研究结果表明:在复合材料固化反应的过程中,外观以中空的球形为多、聚集态结构以无定形结构为主的SFP能够在复合材料中形成明显的孔。随着SFP比例增加,复合材料表面的孔有增多趋势,SFP数量多少对复合材料的最大孔径有影响,随着SFP比例增加,最大孔径有增大趋势。复合材料中由SFP形成孔的直径范围在15.2μm-284.6μm之间;固相为含5%SFP、10%CSH的复合材料,在液固比大于等于0.45时,平均孔径无明显差异,但均大于液固比0.40时复合材料的平均孔径;CSH比例对复合材料中孔的大小和数量无明显影响。复合材料固化反应4h的固化体已经有产物HA生成,在7周内,随着固化时间的延长HA不断生成。材料中的DCPA在1周内转化为HA,而TTCP到7周时还未完全转化为HA。不同SFP比例复合材料表面均有片状和针状的HA晶体;不同CSH比例复合材料中均有针状的HA晶体;固相成分均为含5%SFP、10%CSH的复合材料,当液固比为0.40时以柱状HA晶体为主,当液固比为0.45和0.50时以针状HA晶体以为主,当液固比为0.55时以片状HA晶体为主。含SFP复合材料的孔隙率(大于53%)均高于纯CPC(46.81%),当复合材料中SFP比例小于5%时,随着SFP比例的增加材料的孔隙率从49.3%提高到59.4%;当SFP比例大于5%时,随着SFP比例的进一步增加孔隙率有所下降;随着复合材料中CSH比例从0%增加到30%,材料的孔隙率从55.7%上升到61.6%;随液固比的增加材料孔隙率也有增加的趋势。复合材料的压缩强度和压缩断裂功均随着材料中SFP比例增加而提高,复合材料中SFP比例达10%时材料的压缩强度达到7.3MPa,复合材料中SFP比例达10%时材料的压缩断裂功达到330.3mJ,明显高于不含SFP的复合材料的174.8mJ;复合材料的压缩强度和压缩断裂功都随着材料中CSH比例或液固比的增加而降低。在本实验确定的液固比条件下,不同SFP比例、不同CSH比例的复合材料的凝固时间无明显差异,都在13-16min之间,注射性也无明显差异,所有样品的注射率均在90%以上。液固比对复合材料的凝固时间和注射性能有明显影响,随液固比的增加材料的凝固时间延长,注射率增加,尤其当液固比从0.40增加到0.45复合材料的注射率从44.9%增加到84.3%。纯CPC和不含CSH的SFP/CPC复合材料的重量在SBF中的前五周呈现增加趋势。含有CSH的复合材料在SBF的3周时间里,随着时间延长样品重量有所减少。从第3到第5周样品的重量出现增加,第5周后重量出现下降的趋势。纯CPC样品随着在SBF中时间的延长样品表面孔洞无明显的变化,结构仍致密;不含SFP含10%比例CSH的复合材料随着在SBF中时间的延长,样品表面的微孔数量有增加趋势;含5%SFP、10%CSH的复合材料和含10%SFP、10%CSH的复合材料在SBF中均随着时间的延长,材料变得有些松;不含CSH含5%SFP的复合材料随着在SBF中时间延长,材料的表面形态无明显差异。

【Abstract】 In this paper, the SF/CPC/CSH composites which have good injectablity and canbe solidified and form pores in situ was prepared, this composites composed of thecalcium phosphate cement (CPC) and the silk fibroin particle (SFP) microspheres whichwas mainly amorphous structure. The influence of the proportion of SFP, the proportionof calcium sulfate hemihydrate (CSH) and liquid to powder (L/P) ratio on the structureand properties of composites were studied, and the change of structure and properties ofsamples when immersed in SBF were investigated. The results showed that the SFwhich had the morphology of a hollow sphere was prepared, and the aggregationstructure of the SFP was mainly the amorphous. The SFP could form obvious pores incomposites, the number and the largest pore size of pores had increased trend with theincreased proportion of SFP. The size of pore which was formed by SFP ranged from15.2μm to284.6μm. The composites which had5%of SFP and10%of CSH wereprepared by the L/P ratio greater than or equal to0.45ml/g, and the average size of thepores in these composites had not significant difference, but all larger than the averagesize of pores in the composites which prepared by the L/P ratio to0.40ml/g. Theproportion of CSH had no significant effect on the number and size of pores incomposites.The composites started up setting reaction and transformed into HA in seven weeks.The dicalcium phosphate anhydrous transformed into HA in the first week, but thetetracalcium phosphate was not totally transformed and still contained after seven weeks.The surface of composites which had different proportion of SFP all had platelet-likeand needle-like HA crystals. The surface of composites which had different ratio ofCSH all were mainly needle-like HA crystals. The surface of composites which had5%of SFP and10%of CSH were mainly rod-like HA crystals when this compositesprepared by the L/P ratio to0.40ml/g, and the surface of the composites were mainlyneedle-like HA crystals when prepared by the L/P ratio to0.45ml/g and0.50ml/g, andthe surface of composites were mainly platelet-like HA crystals when prepared by theL/P ratio to0.50ml/g. The average porosity of composites which contained SFP was larger than53%, andthe average porosity of the pure CPC was46.8%. The porosity had increased from49.3%to59.4%with the increased proportion of SFP when the proportion was less than5%, but the porosity had decreased trend with the increased proportion of SF when theproportion was higher than5%. The porosity had increased from55.7%to61.6%withthe increased proportion of CSH from0%to30%of the composites.The porosity hadincreased trend with the increased L/P ratio.The compressive strength and work-of-compressive of composites had increasedtrend with the increased proportion of SFP, but had decreased trend with the increasedproportion of CSH or the increased L/P ratio.Under the L/P ratio conditions of this experiment, there had no significantdifferences of setting time and injectability between the composites which had differentSF proportion and the composites which had different CSH proportion. All setting timeof composites were within the range of13min to16min, and all the injection rate wereabove90%. The L/P ratio had a significant effect on the setting time and injection ratioof composites, the setting time extended and the injection rate increased with increasedof the L/P ratio, and the injection rate of composites increased from44.9%to84.3%when the L/P ratio increased from0.40ml/g to0.45ml/g.The weight of CPC and SFP/CPC composites had increased trend when thesamples immersed in SBF in five weeks. The weight of composites which containedCSH had decreased trend when the composites immersed in SBF in three weeks, but theweight had slightly increased from the third week to the fifth week, and the weight haddecreased trend after five weeks. The pores of pure CPC had not significant changesand still dense when the composites immersed in SBF. The surface of composites whichhad10%of CSH appeared more and more microporous with time extended when thecomposites immersed in SBF. The composites which contained SFP and CSH becomesomewhat loose with time extended when the composites immersed in SBF, The surfacemorphology of composites which without CSH had no significant difference with timeextended when the composites immersed in SBF.

  • 【网络出版投稿人】 苏州大学
  • 【网络出版年期】2012年 10期
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