纳米羟基磷灰石-胶原和表没食子儿茶素-没食子酸酯(EGCG)复合材料的扫描电镜-能谱(SEM-EDS)、x射线衍射(XRD)和傅里叶变换红外(FTIR)表征

Elline, Eko Fibryanto, Hiroko Amanda
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引用次数: 1

摘要

背景:氢氧化钙(Ca(OH)2)是生命牙髓治疗中最常用的药物,是牙髓覆盖材料的金标准;然而,它显示出一些局限性,包括易于溶解、刺激具有隧道缺陷的修复性牙本质和炎症。先前的一项研究报道,纳米羟基磷灰石(nHA)可能比Ca(OH)2更好地诱导无隧道缺陷的修复性牙本质。另一项研究报道,在胶原凝胶中添加表没食子儿茶素-3-没食子酸盐(EGCG)可以通过改变其力学性能来增加牙髓细胞的增殖和分化。目的:采用扫描电子显微镜能谱仪(SEM-EDS)、X射线衍射仪(XRD)和傅立叶变换红外光谱(FTIR)对nHA–Col和EGCG复合材料进行了表征。方法:将每种材料(即nHA、Col 1型和EGCG)溶于2 mL去离子水。制备了具有不同nHA:Col比率的三组:40:60(第1组)、50:50(第2组)和60:40(第3组)。使用磁力搅拌器在40°C下将每种溶液混合在一起,然后向混合物中加入2%羟丙基甲基纤维素(HPMC)。通过SEM-EDS、XRD和FTIR对形貌观察、钙磷比、晶相分析和官能团分析进行了研究。结果:SEM-EDS分析显示Col原纤维之间存在不规则的团聚nHA,Ca/P比为非化学计量比(>1.67)。XRD分析显示为六方相nHA。FTIR分析揭示了nHA、Col和EGCG之间的化学相互作用。结论:SEM-EDS和XRD分析证实,nHA与Col和EGCG混合时不会发生变化,FTIR分析显示材料之间存在氢键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of nano-hydroxyapatite–collagen and epigallocatechin-3-gallate (EGCG) composites by scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS), X-ray diffraction (XRD), and Fourier transform infrared (FTIR) spectroscopy
Background: Calcium hydroxide (Ca(OH)2) is most commonly used in vital pulp therapy, and it is the gold standard of pulp capping materials; however, it shows several limitations, including facile dissolution, stimulation of reparative dentin with tunnel defects, and inflammation. A previous study reported that nano-hydroxyapatite (nHA) might induce reparative dentin with no tunnel defects much better than Ca(OH)2. Another study reported that the addition of epigallocatechin-3-gallate (EGCG) to collagen (Col) gel can increase pulp cell proliferation and differentiation via the change in its mechanical properties. Objective: In this study, nHA–Col and EGCG composites were characterized by scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS), X-ray diffraction (XRD), and Fourier transform infrared (FTIR) spectroscopy. Methods: Each material (i.e., nHA, Col type 1, and EGCG) was dissolved in 2 mL of deionized water. Three groups with varied nHA:Col ratios were prepared: 40:60 (group 1), 50:50 (group 2), and 60:40 (group 3). Each solution was mixed together using a magnetic stirrer at 40°C, followed by the addition of 2% hydroxypropyl methylcellulose (HPMC) into the mixture. Morphology observation, Ca/P ratio, crystallographic phase analysis, and functional group analysis were investigated by SEM-EDS, XRD, and FTIR. Results: SEM-EDS analysis revealed irregular agglomerated nHA between Col fibrils and a non-stoichiometric Ca/P ratio (>1.67). XRD analysis revealed hexagonal-phase nHA. FTIR analysis revealed chemical interaction between nHA, Col, and EGCG. Conclusions: SEM-EDS and XRD analysis confirmed that nHA does not change when it is mixed with Col and EGCG, and FTIR analysis revealed hydrogen bonding among materials.
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