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评价改良唾液替代物的体外再矿化能力。

Evaluation of the remineralizing capacities of modified saliva substitutes in vitro.

机构信息

Department of Operative Dentistry and Periodontology, CharitéCentrum 3, University School for Dental Medicine, Charité-Universitätsmedizin Berlin, Germany.

出版信息

Arch Oral Biol. 2009 Sep;54(9):810-6. doi: 10.1016/j.archoralbio.2009.06.004.

Abstract

OBJECTIVE

In this in vitro study the effects of various calcium and phosphate additions to a commercially available saliva substitute on remineralization of demineralised dentin were investigated.

DESIGN

Bovine dentin specimens (n=70) were prepared. Before and after demineralisation (37 degrees C, pH 5.0, 5 days), one-quarter of each specimens surface was covered with nail varnish (control sound/demineralised tissue). Specimens were exposed either to original Saliva natura (SN 0) or to three modified versions (SN 1, SN 2 and SN 3) formulated with different degrees of saturation with respect to octacalciumphosphate (OCP) and dicalcium phosphate dihydrate (DCPD) for 2 and 5 weeks (37 degrees C). An aqueous solution (Buskes remineralizing solution) served as positive control (PC). Differences in mineral loss (deltadeltaZ) and lesion depth (deltaLD) before and after storage were evaluated from microradiographs.

RESULTS

After both storage periods dentin specimens immersed in SN 0 revealed significantly higher mineral losses (indicated by deltadeltaZ) and higher lesion depths (indicated by deltaLD) compared to all other solutions (p<0.05; ANOVA). Specimens stored in SN 1 and 3 showed significantly higher mineral losses compared with PC (p<0.05). No differences could be observed between SN 2 and PC (p>0.05). Only SN 2 significantly remineralized from 2 to 5 weeks storage (p<0.05; t-test).

CONCLUSIONS

An experimental Saliva natura solution (SN 2) with S(OCP)=2 and S(DCPD)=1.4 showed highest remineralizing capacity. Similar or better remineralization could not be achieved with slightly higher or lower saturated solutions.

摘要

目的

本体外研究旨在探讨在商业上可获得的唾液替代品中添加不同钙和磷酸盐对脱矿牙本质再矿化的影响。

设计

制备牛牙本质标本(n=70)。在脱矿化(37°C,pH 5.0,5 天)前后,每个标本表面的四分之一用指甲油覆盖(对照完好/脱矿化组织)。标本分别暴露于原始唾液自然(SN 0)或三种改良版本(SN 1、SN 2 和 SN 3)中,这些版本在八钙磷酸盐(OCP)和二水磷酸二钙(DCPD)的饱和度方面具有不同程度的饱和度,持续 2 和 5 周(37°C)。水溶液(Buskes 再矿化溶液)作为阳性对照(PC)。从微射线照片评估储存前后的矿物损失(deltadeltaZ)和病变深度(deltaLD)差异。

结果

在两个储存期后,与所有其他溶液相比,浸泡在 SN 0 中的牙本质标本显示出明显更高的矿物损失(由 deltadeltaZ 表示)和更高的病变深度(由 deltaLD 表示)(p<0.05;ANOVA)。与 PC 相比,储存在 SN 1 和 3 中的标本显示出明显更高的矿物损失(p<0.05)。在 SN 2 和 PC 之间未观察到差异(p>0.05)。仅 SN 2 在 2 至 5 周的储存期间表现出明显的再矿化(p<0.05;t 检验)。

结论

具有 S(OCP)=2 和 S(DCPD)=1.4 的实验性唾液自然(SN 2)溶液显示出最高的再矿化能力。稍微增加或降低饱和度的溶液无法实现类似或更好的再矿化。

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