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基于实验设计法合成羟基磷灰石/生物玻璃复合纳米粉末

Synthesis of Hydroxyapatite/Bioglass Composite Nanopowder Using Design of Experiments.

作者信息

Ebrahimi Shamsi, Sipaut Coswald Stephen

机构信息

Faculty of Engineering, Universiti Malaysia Sabah, UMS Road, Kota Kinabalu 88400, Malaysia.

出版信息

Nanomaterials (Basel). 2022 Jun 30;12(13):2264. doi: 10.3390/nano12132264.

DOI:10.3390/nano12132264
PMID:35808097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9268266/
Abstract

Composite scaffolds of hydroxyapatite (HAp) nanoparticles and bioactive glass (BG) were applied as an appropriate selection for bone tissue engineering. To this end, HAp/BG composite was synthesized by a hydrothermal method using Design of Experiments (DOE) with a combined mixture-process factor design for the first time. The input variables were hydrothermal temperature at three levels (i.e., 100, 140, 180 °C) as a process factor and two mixture components in three ratios (i.e., HAp 90, 70, 50; BG 50, 30, 10). The degree of crystallinity and crystal size in the composite were the output variables. XRD showed that only a small fraction of BG was crystallized and that a wollastonite phase was produced. The XRD results also revealed that incorporation of Si into the HAp structure inhibited HAp crystal growth and restricted its crystallization. The FTIR results also showed that the intensity of the hydroxyl peak decreased with the addition of silicon into the HAp structure. DOE results showed that the weight ratio of the components strongly influenced the crystal size and crystallinity. SEM and FTIR results identified the greatest bioactivity and apatite layer formation in the Si-HAp sample with an HAp70/BG30 ratio after 14 days immersion in simulated body fluid (SBF) solution, as compared to other ratios and HAp alone. Therefore, the combination of HAp and BG was able to yield a HAp/BG composite with significant bioactivity.

摘要

羟基磷灰石(HAp)纳米颗粒与生物活性玻璃(BG)的复合支架被用作骨组织工程的合适选择。为此,首次采用实验设计(DOE)的水热法,通过混合过程因子联合设计合成了HAp/BG复合材料。输入变量为作为过程因子的三个温度水平(即100、140、180°C)的水热温度以及两种以三种比例混合的成分(即HAp 90、70、50;BG 50、30、10)。复合材料中的结晶度和晶体尺寸为输出变量。X射线衍射(XRD)表明,只有一小部分BG结晶,并且生成了硅灰石相。XRD结果还表明,Si掺入HAp结构中会抑制HAp晶体生长并限制其结晶。傅里叶变换红外光谱(FTIR)结果还表明,随着硅掺入HAp结构中,羟基峰的强度降低。DOE结果表明,各成分的重量比强烈影响晶体尺寸和结晶度。扫描电子显微镜(SEM)和FTIR结果表明,与其他比例以及单独的HAp相比,在模拟体液(SBF)溶液中浸泡14天后,HAp70/BG30比例的Si-HAp样品具有最大的生物活性和磷灰石层形成。因此,HAp和BG的组合能够产生具有显著生物活性的HAp/BG复合材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/158181c7f114/nanomaterials-12-02264-g013.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/069a3d37f4f1/nanomaterials-12-02264-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/a500c11c7a60/nanomaterials-12-02264-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/8c79c822ea4b/nanomaterials-12-02264-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/1cdbe76556d6/nanomaterials-12-02264-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/fbc51b772abd/nanomaterials-12-02264-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/041ed5e8ce20/nanomaterials-12-02264-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/158181c7f114/nanomaterials-12-02264-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/04e7624f499d/nanomaterials-12-02264-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/245a682c2e26/nanomaterials-12-02264-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/7153894c4665/nanomaterials-12-02264-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/22edb02b2ef6/nanomaterials-12-02264-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/0510f86abd95/nanomaterials-12-02264-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/df8679d8fa3c/nanomaterials-12-02264-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/069a3d37f4f1/nanomaterials-12-02264-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/a500c11c7a60/nanomaterials-12-02264-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/8c79c822ea4b/nanomaterials-12-02264-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/1cdbe76556d6/nanomaterials-12-02264-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/fbc51b772abd/nanomaterials-12-02264-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/041ed5e8ce20/nanomaterials-12-02264-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c390/9268266/158181c7f114/nanomaterials-12-02264-g013.jpg

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