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通过顺序暴露于次氯酸钠和 EDTA 评估人牙本质中磷灰石和胶原蛋白的降解深度:一项定量 FTIR 研究。

Estimated depth of apatite and collagen degradation in human dentine by sequential exposure to sodium hypochlorite and EDTA: a quantitative FTIR study.

机构信息

Unit of Endodontology, Department of Restorative Dentistry, UCL Eastman Dental Institute, University College London, London, UK.

Division of Biomaterials and Tissue Engineering, UCL Eastman Dental Institute, University College London, London, UK.

出版信息

Int Endod J. 2018 Apr;51(4):469-478. doi: 10.1111/iej.12864. Epub 2017 Nov 1.

Abstract

AIM

To characterize chemical degradation of the principal constituents of dentine after exposure to NaOCl and EDTA using Infrared Spectroscopy (ATR-FTIR).

METHODOLOGY

Ground dentine particles, from extracted permanent human molars, were passed through sieves of 38 to 1 000 μm to provide six size ranges. Portions (250 mg) of each size range were reacted with 5 mL of 2.5% NaOCl for 2-10 min; or 17% EDTA for 5-1440 min. Powders larger than 75 μm were also sequentially exposed to NaOCl/EDTA/NaOCl each for 10 min. All experiments were repeated five times. Reacted and unreacted powders were washed and dried. Particles larger than 75 μm were then reground. FTIR spectra of unground and reground reacted particles enabled assessment of particle surface versus bulk chemistry, respectively, plus estimation of reaction depth. Changes in the ratio of the 1 640 cm collagen: 1 010 cm phosphate peak height or its inverse were obtained. These were used to estimate surface and bulk fraction reacted and thus depth to which collagen or phosphate was reduced following immersion in NaOCl or EDTA, respectively. The data were analysed descriptively.

RESULTS

Surface collagen fraction declined by ~40% within 2 min of NaOCl exposure, and plateaued at ~60% between 6-10 min. Bulk spectra showed average depth of collagen loss at 10 min was 16 ± 13 μm. Ten minute EDTA exposure caused ~60% loss of surface phosphate. Average depth of phosphate loss was 19 ± 12 μm and 89 ± 43 μm after 10 and 1 440 min EDTA immersion, respectively. Sequential NaOCl/EDTA immersion yielded a 62 ± 28 μm thick phosphate-depleted surface. Sequential NaOCl/EDTA/NaOCl treatment resulted in approximately 85 μm of collagen loss.

CONCLUSIONS

Data revealed the sequential depletion of collagen by NaOCl and apatite by EDTA in dentine, simultaneously exposing the other moieties. Alternate exposure to NaOCl and EDTA therefore enhances the depth of erosion.

摘要

目的

使用红外光谱(ATR-FTIR)表征暴露于次氯酸钠和 EDTA 后牙本质主要成分的化学降解。

方法

从提取的人恒磨牙中研磨牙本质颗粒,通过 38 至 1000μm 的筛子,提供六个粒径范围。每个粒径范围的部分(250mg)与 5mL 2.5%次氯酸钠反应 2-10 分钟;或 17%EDTA 反应 5-1440 分钟。大于 75μm 的粉末也分别连续暴露于次氯酸钠/EDTA/次氯酸钠各 10 分钟。所有实验均重复五次。反应和未反应的粉末均经洗涤和干燥。然后将大于 75μm 的颗粒再次研磨。对未研磨和再研磨的反应颗粒进行 FTIR 光谱分析,分别评估颗粒表面与体相化学,以及估计反应深度。获得胶原 1640cm 处峰与磷酸 1010cm 处峰高度的比值或其倒数的变化。这些用于估计表面和体相反应部分,从而分别估计胶原蛋白或磷酸盐在浸入次氯酸钠或 EDTA 后的减少深度。数据进行描述性分析。

结果

暴露于次氯酸钠 2 分钟内,表面胶原分数下降约 40%,6-10 分钟时达到约 60%的平台。体相光谱显示,10 分钟时胶原的平均损失深度为 16±13μm。10 分钟 EDTA 暴露导致表面磷酸盐损失约 60%。10 分钟和 1440 分钟 EDTA 浸泡后,磷酸盐的平均损失深度分别为 19±12μm 和 89±43μm。次氯酸钠/EDTA 交替浸泡产生 62±28μm 厚的磷酸盐耗尽表面。次氯酸钠/EDTA/次氯酸钠处理导致约 85μm 的胶原蛋白损失。

结论

数据显示次氯酸钠依次耗尽牙本质中的胶原蛋白,EDTA 耗尽牙本质中的磷灰石,同时暴露其他部分。交替暴露于次氯酸钠和 EDTA 因此会增加侵蚀深度。

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