Department of Physics, University of Bologna, Viale Berti Pichat 6/2, 40127 Bologna, Italy.
J Phys Chem B. 2010 Feb 11;114(5):1767-74. doi: 10.1021/jp907248r.
Time-domain nuclear magnetic resonance (TD-NMR) of (1)H nuclei has been used to monitor and model changes of endodontic cement pastes during hydration, from the initial reaction period up to hours and days. The (1)H in the samples are divided into two major spin groups by fitting each free induction decay, acquired after the second pulse of an inversion recovery (I-R) pulse sequence with variable interpulse delay, by the sum of a quasi-Gaussian (signal from low mobility nuclei) and an exponential (from higher mobility nuclei). The extrapolations to zero time of the signals from the two spin groups give two sets of I-R data that have been analyzed to give quasi-continuous T(1) distributions. After about a day, two clearly solid components appear. From a day to a few days, three liquid populations are identified, one of them mainly in the low-mobility spin group, which later merge, giving a single T(1) or T(2) peak. The rapid onset of the solid components, at the cost of the liquid, and the rapid changes of the relaxation time distributions of all components are clear indicators of the amount and kinetics of reaction products formation (C-S-H gel and Portlandite) and of the C-S-H micronanoporous structure buildup and evolution. At 30 days of hydration, the very short T(1) and T(2) liquid component (T(1) congruent with 200 micros and T(2) congruent with 50 micros) can be assigned to C-S-H intralayer water (thickness of the order of fractions of a nanometer) and the remaining liquid signal to interlayer water (thickness of the order of 1 nm). Comparisons are made among a widely used commercial endodontic cement paste and two more recent commercial pastes, with additive compounds to make the hydration process faster and to increase the workability. Parameters can be extracted from the data to characterize the different kinetics and nanostructure of the pore space formed up to 30 days. The parameters are in agreement with the expected effects of the additives, so the parameters can be used to optimize the formulation of new pastes, in order to improve their therapeutic performance.
利用时域核磁共振(TD-NMR)对核(1)H 进行监测和建模,以研究牙根管水泥糊剂在水化过程中的变化,监测时间从最初的反应期到数小时和数天。将样品中的(1)H 核按两组主要自旋分类,通过对反转恢复(I-R)脉冲序列第二个脉冲之后获得的每个自由感应衰减(FID)进行拟合,拟合方法是将其分解为拟高斯(低流动性核的信号)和指数(高流动性核的信号)之和。两组自旋信号的零时间外推给出了两组 I-R 数据,这些数据已经过分析以给出准连续 T1 分布。大约一天后,出现了两个明显的固体相。从一天到几天,鉴定出了三种液相,其中一种主要在低流动性自旋组中,后来合并为一个单 T1 或 T2 峰。固体相的快速形成(以牺牲液相为代价)和所有相的弛豫时间分布的快速变化是反应产物(C-S-H 凝胶和波特兰石)形成量和动力学以及 C-S-H 微孔纳米结构的构建和演变的明显指标。水化 30 天后,非常短的 T1 和 T2 液体(T1 约为 200 微秒,T2 约为 50 微秒)可以分配给 C-S-H 层间水(厚度约为纳米分数),剩余的液体信号分配给层间水(厚度约为 1nm)。将一种广泛使用的商业根管水泥糊剂与两种较新的商业糊剂进行了比较,这两种商业糊剂都添加了化合物以加速水化过程并提高可操作性。可以从数据中提取参数来描述 30 天内形成的不同动力学和纳米孔结构。这些参数与添加剂的预期效果一致,因此可以使用这些参数来优化新糊剂的配方,以提高其治疗性能。