脂肪酸螯合临时牙水泥中十六烷基吡啶氯的释放。

Andrew Hurt, Nichola J Coleman, Tamer Tüzüner, Bora Bagis, Fatih Mehmet Korkmaz, John W Nicholson
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引用次数: 4

摘要

目的观察添加5%十六烷基吡啶氯(CPC)是否能提高脂肪酸螯合临时性牙水泥的抗菌性能。材料和方法采用临时水泥Cavex temporary,在混合水泥之前,将CPC添加到基础或催化剂膏体中。在样品制备后的2周内,使用反相高效液相色谱法跟踪水泥样品中CPC的释放情况。利用傅里叶变换红外光谱(FTIR)检测Cavex和CPC之间的潜在相互作用,并在培养的变形链球菌培养皿中检测24 h后的抑菌带。结果FTIR显示CPC与水泥组分之间没有相互作用。发现CPC释放在前6小时左右遵循扩散机制,并在大约2周后达到平衡,当添加剂加入到碱或催化剂膏体中时,释放曲线没有显着差异。扩散速度快,扩散系数约为1 × 10-9 m2 s-1。总释放量为CPC加载量的10-12%。含CPC水泥环周围的抑制区明显大于不含CPC水泥环周围的抑制区。结论CPC的加入可提高该临时水泥的抗菌性能。这种增强具有潜在的临床价值,尽管需要进一步的体内工作来证实这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Release of cetyl pyridinium chloride from fatty acid chelate temporary dental cement.

Release of cetyl pyridinium chloride from fatty acid chelate temporary dental cement.

Release of cetyl pyridinium chloride from fatty acid chelate temporary dental cement.

Release of cetyl pyridinium chloride from fatty acid chelate temporary dental cement.

Objective To determine whether the antimicrobial nature of a fatty acid chelate temporary dental cement can be enhanced by the addition of 5% cetyl pyridinium chloride (CPC). Materials and methods The temporary cement, Cavex Temporary was employed, and additions of CPC were made to either the base or the catalyst paste prior to mixing the cement. Release of CPC from set cement specimens was followed using reverse-phase HPLC for a period of up to 2 weeks following specimen preparation. Potential interactions between Cavex and CPC were examined by Fourier transform infrared spectroscopy (FTIR) and antimicrobial effects were determined using zone of inhibition measurements after 24 h with disc-shaped specimens in cultured Streptococcus mutans. Results FTIR showed no interaction between CPC and the components of the cement. CPC release was found to follow a diffusion mechanism for the first 6 h or so, and to equilibrate after approximately 2 weeks, with no significant differences between release profiles when the additive was incorporated into the base or the catalyst paste. Diffusion was rapid, and had a diffusion coefficient of approximately 1 × 10-9 m2 s-1 in both cases. Total release was in the range 10-12% of the CPC loading. Zones of inhibition around discs containing CPC were significantly larger than those around the control discs of CPC-free cement. Conclusions The antimicrobial character of this temporary cement can be enhanced by the addition of CPC. Such enhancement is of potential clinical value, though further in vivo work is needed to confirm this.

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