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Bioactive glass composite for orthodontic adhesives - Formation and characterisation of apatites using MAS-NMR and SEM

机译:正畸胶粘剂用生物活性玻璃复合材料-用MAS-NMR和SEM表征磷灰石的形成和表征

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摘要

Objectives. To study the dissolution and fluoroapatite (FAP) formation of a new bioactive glass (BAG)-resin adhesive in an acidic solution in reference to neutral solutions, using the magic angle spinning-nuclear magnetic resonance (MAS-NMR) and the scanning electron microscopy (SEM).Methods. BAG composite disks (n = 90) were prepared from, novel fluoride-containing BAG-resin. Three sample groups (n = 30) of the disks were immersed in Tris buffer pH = 7.3 (TB), neutral artificial saliva pH = 7 (AS7) and acidic artificial saliva pH = 4 (AS4) at ten time points ( from 6 h to 6 months). Half of the immersed disks at each time point were crushed into a powder and investigated by the solid state MAS-NMR. SEM studies were undertaken by embedding the other half of the immersed disk in a self-cure acrylic where the fracture surface was imaged.Results. MAS-NMR results show that the BAG composite degraded significantly faster in AS4 compared to TB and AS7. At the end of the immersion period (6 months), around 80% of the glass particles in AS4 had reacted to form an apatite, evidenced by the sharp peak at 2.82 ppm in P-31 signals compared to a broader peak in TB and AS7. It also shows evidence of fluorapatite (FAP) formation, indicated by F-19 signal at -103 ppm, while signal around -108 ppm indicated the formation of calcium fluoride, from the excess Ca2+ and F- especially on longer immersion. SEM images confirm higher degradation rate of the BAG composite in AS4 and reveal the impact of time on the dissolution of more glass particles. The images also indicate apatite formation around the glass particles in TB and AS4, while it forms predominantly over the disk surface in AS7.Significance. BAG composite demonstrate smart reactivity in response to pH change which has a potential clinical benefit against demineralization and promoting remineralisation to form more stable fluorapatites. (C) 2019 The Academy of Dental Materials. Published by Elsevier Inc. All rights reserved.
机译:目标。使用魔角旋转核磁共振(MAS-NMR)和扫描电子显微镜研究酸性溶液中相对于中性溶液的新型生物活性玻璃(BAG)-树脂粘合剂的溶解和氟磷灰石(FAP)的形成(SEM)。方法。用新型的含氟BAG树脂制备BAG复合盘(n = 90)。在十个时间点(从6小时开始),将三个样品组(n = 30)的圆盘浸入Tris缓冲液pH = 7.3(TB),中性人工唾液pH = 7(AS7)和酸性人工唾液pH = 4(AS4)中至6个月)。将每个时间点的一半浸没圆盘压成粉末,并通过固态MAS-NMR进行研究。 SEM研究是通过将浸没盘的另一半嵌入自固化丙烯酸树脂中进行的,其中对断裂表面进行了成像。 MAS-NMR结果表明,与TB和AS7相比,AS4中BAG复合材料的降解明显更快。在浸没阶段(6个月)结束时,AS4中约80%的玻璃颗粒反应形成了磷灰石,这与P-31信号中2.82 ppm的尖峰相比,而TB和AS7的峰更宽。它还显示了氟磷灰石(FAP)形成的证据,F-19信号在-103 ppm处指示,而-108 ppm左右的信号则表示由过量的Ca2 +和F-形成氟化钙,尤其是在更长的浸泡时间下。 SEM图像证实了AS4中BAG复合材料的较高降解速率,并揭示了时间对更多玻璃颗粒溶解的影响。这些图像还表明在TB和AS4中玻璃颗粒周围形成了磷灰石,而在AS7中它主要形成在圆盘表面上。 BAG复合材料显示出对pH值变化的灵敏反应性,具有潜在的临床益处,可防止脱矿质并促进再矿化以形成更稳定的氟磷灰石。 (C)2019牙科材料学院。由Elsevier Inc.出版。保留所有权利。

著录项

  • 来源
    《Dental materials》 |2019年第4期|597-605|共9页
  • 作者单位

    Queen Mary Univ London, Barts & London Sch Med & Dent, Inst Dent, Ctr Oral Bioengn, Mile End Rd, London E1 4NS, England|Univ Anbar, Coll Dent, Dept Paediat Orthodont & Prevent Dent, POB 55, Ramadi, Iraq;

    Queen Mary Univ London, Barts & London Sch Med & Dent, Inst Dent, Ctr Oral Bioengn, Mile End Rd, London E1 4NS, England;

    Queen Mary Univ London, Barts & London Sch Med & Dent, Inst Dent, Ctr Oral Bioengn, Mile End Rd, London E1 4NS, England;

    Queen Mary Univ London, Barts & London Sch Med & Dent, Inst Dent, Ctr Oral Bioengn, Mile End Rd, London E1 4NS, England;

    Queen Mary Univ London, Barts & London Sch Med & Dent, Inst Dent, Ctr Oral Bioengn, Mile End Rd, London E1 4NS, England;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Bioactive glass; Fluorapatite; White spot lesions; Orthodontic adhesives; MAS-NMR; SEM;

    机译:生物活性玻璃;氟磷灰石;白斑病变;正畸胶粘剂;MAS-NMR;SEM;

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