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

机译:用于正畸粘合剂的生物活性玻璃复合材料 - 使用MAS-NMR和SEM形成和表征磷灰石

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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。研究溶解和氟磷灰石(FAP)在酸性溶液中形成新的生物活性玻璃(袋)粘合剂,参考中性溶液,使用魔法角旋转核磁共振(MAS-NMR)和扫描电子显微镜(SEM)。方法。袋复合磁盘(n = 90)由新型氟化物袋树脂制备。将磁盘的三个样品基团(n = 30)浸入Tris缓冲液pH = 7.3(TB)中,中性人工唾液pH = 7(AS7)和酸性人工唾液pH = 4(AS4)(从6小时到6个月)。每次点的一半浸没盘被粉碎成粉末并由固态Mas-NMR研究。通过将其他一半的浸渍盘嵌入自我固化的丙烯酸中来进行SEM研究,其中裂缝表面被成像。结果。 MAS-NMR结果表明,与TB和AS7相比,AS4的袋子复合材料在AS4上显着降低。在浸入期(6个月)的末端,AS4中的约80%的玻璃颗粒反应形成磷灰石,与TB和AS7中的更广泛的峰相比,在P-31信号中的2.82ppm下的尖峰证明。它还显示出氟磷酸盐(FAP)形成的证据,在-103ppm下由F-19信号表示,而左右-108ppm的信号表明氟化钙的形成,来自过量的Ca2 +和f-特别是在较长的浸渍中。 SEM图像在AS4中确认袋子复合材料的更高降解速率,并揭示了时间对更多玻璃颗粒溶解的影响。图像还指示Tb和AS4中的玻璃颗粒周围的磷灰石形成,同时它在AS7的圆盘表面上主要形成。袋子复合材料表现出智能反应性,响应pH改变,潜在的临床效益免受脱矿质和促进催化形成更稳定的氟磷灰石。 (c)2019年牙科材料学院。由elsevier Inc.出版的所有权利保留。

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;正畸粘合剂;MAS-NMR;SEM;

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