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High-strength and tough bioactive Mg-doped hydroxyapatite bioceramics with oriented microchannels

机译:具有定向微通道的高强度和坚韧生物活性镁掺杂羟基磷灰石生物陶瓷

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Mg-doped hydroxyapatite (MH) with oriented microchannels was prepared by hot-pressing sintering and pore forming heat treatment using continuous carbon fibres (CFs) as the pore-forming agent to achieve balanced mechanical and biological properties. The proportion of MH and (Ca, Mg)(3)(PO4)(2) in the microporous bioceramic with inter-microchannel spacing of 400 mu m obtained by sintering at 900 degrees C (900-2P-MH) was 43.9/56.1 (wt), which could promote degradation. The compressive strength of the MH bioceramics containing oriented microchannels with a suitable pore size (5-14 mu m) did not decrease, but increased in comparison with that of a dense MH sample without microchannels. In particular, the compression strength of the MH bioceramic with oriented microchannels formed using single CF units was 53.31 higher than that of the dense ones. The fracture toughness of the MH bioceramics with oriented microchannels increased to 177.42 of that of the dense ones. The strengthening and toughening mechanism includes contributions from the combination of heating and pressing, uniform distribution of microchannels, and in situ formation of continuous micro/nano-MH ceramic tubes. Moreover, the microchannel-containing MH showed noticeably improved apatite mineralisation in simulated body fluid (SBF). Analysis of the rat tibial bone defect model revealed that the relative bone volumes in the cases of the dense MH without microchannels and the MH with microchannels increased by 23.18 and 40.14, respectively, compared with that of hydroxyapatite. Furthermore, the MH bioceramics with oriented microchannels displayed a moderate reduction in strength owing to degradation after 8 weeks of implantation. The satisfactory osteogenic properties and degradability of the microporous bioceramic can be attributed to Mg2+ doping and oriented microchannels.
机译:以连续碳纤维(CFs)为成孔剂,通过热压烧结和成孔热处理制备了具有定向微通道的镁掺杂羟基磷灰石(MH),实现了力学和生物性能的平衡。在900°C(900-2P-MH)烧结得到的微孔间距为400 μ m的微孔生物陶瓷中MH和(Ca, Mg)(3)(PO4)(2)的比例为43.9/56.1 (wt%),可促进降解。与无微通道的致密MH样品相比,含有合适孔径(5-14 μ m)的定向微通道的MH生物陶瓷的抗压强度没有降低,反而有所增加。其中,采用单个CF单元形成的具有定向微通道的MH生物陶瓷的抗压强度比致密的MH生物陶瓷高53.31%。具有定向微通道的MH生物陶瓷的断裂韧性提高到致密微通道的177.42%。强化增韧机理包括加热和压制相结合、微通道均匀分布以及连续微/纳米MH陶瓷管的原位形成。此外,含有微通道的MH在模拟体液(SBF)中显示出明显改善的磷灰石矿化。对大鼠胫骨缺损模型的分析表明,无微通道致密MH和有微通道MH的相对骨体积增加了23。与羟基磷灰石相比,分别为18%和40.14%。此外,具有定向微通道的MH生物陶瓷在植入8周后由于降解而显示出强度的适度降低。微孔生物陶瓷令人满意的成骨性能和降解性可归因于Mg2+掺杂和定向微通道。

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