Rapid Intrafibrillar Mineralization Strategy Enhances Adhesive–Dentin Interface

牙本质 胶粘剂 矿化(土壤科学) 化学 生物医学工程 材料科学 纳米技术 复合材料 化学工程 图层(电子) 医学 工程类 有机化学 氮气
作者
Gao Xiao,Zhiwei Wang,Hong Yang,Cui Huang
出处
期刊:Journal of Dental Research [SAGE Publishing]
卷期号:103 (1): 42-50 被引量:20
标识
DOI:10.1177/00220345231205492
摘要

Biomimetic mineralization of dentin collagen appears to be a promising strategy to optimize dentin bonding durability. However, traditional postbonding mineralization strategies based on Ca/P ion release still have some drawbacks, such as being time-consuming, having a spatiotemporal mismatch, and having limited intrafibrillar minerals. To tackle these problems, a prebonding rapid intrafibrillar mineralization strategy was developed in the present study. Specifically, polyacrylic acid–stabilized amorphous calcium fluoride (PAA-ACF) was found to induce rapid intrafibrillar mineralization of the single-layer collagen model and dentin collagen at just 1 min and 10 min, as identified by transmission electron microscopy, scanning electron microscopy, and atomic force microscopy. This strategy has also been identified to strengthen the mechanical properties of demineralized dentin within a clinically acceptable timeframe. Significantly, the bonding strength of the PAA-ACF–treated groups outperformed the control group irrespective of aging modes. In addition, the endogenous matrix metalloproteinases as well as exogenous bacterial erosion were inhibited, thus reducing the degradation of dentin collagen. High-quality integration of the hybrid layer and the underlying dentin was also demonstrated. On the basis of the present results, the concept of “prebonding rapid intrafibrillar mineralization” was proposed. This user-friendly scheme introduced PAA-ACF–based intrafibrillar mineralization into dentin bonding for the first time. As multifunctional primers, PAA-ACF precursors have the potential to shed new light on prolonging the service life of adhesive restorations, with promising significance.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Lucas应助张敬敬采纳,获得10
刚刚
1秒前
无昵称发布了新的文献求助10
1秒前
2秒前
小甑发布了新的文献求助50
2秒前
阿東要开心完成签到,获得积分10
2秒前
2秒前
忧郁的寻冬完成签到,获得积分10
3秒前
veryzhaozhao发布了新的文献求助10
3秒前
louxinliang发布了新的文献求助10
3秒前
3秒前
3秒前
4秒前
开放芮发布了新的文献求助10
4秒前
烟花应助千与千寻476300采纳,获得10
4秒前
冬日空虚应助外向傲儿采纳,获得10
4秒前
4秒前
天一完成签到,获得积分10
4秒前
5秒前
5秒前
5秒前
6秒前
6秒前
CBWKEYANTONG123完成签到,获得积分10
6秒前
7秒前
7秒前
7秒前
顾矜应助wangshibing采纳,获得10
8秒前
糯米饭完成签到 ,获得积分10
8秒前
小刘鸭的可乐完成签到,获得积分10
8秒前
8秒前
sheep完成签到,获得积分10
8秒前
veryzhaozhao完成签到,获得积分10
8秒前
yu发布了新的文献求助10
9秒前
9秒前
zhu发布了新的文献求助10
9秒前
优秀口红完成签到,获得积分20
10秒前
卷卷发布了新的文献求助10
10秒前
kk发布了新的文献求助10
11秒前
11秒前
高分求助中
Overcoming Stigma and Bias in Obesity Management 800
Malcolm Fraser : a biography 700
Signals, Systems, and Signal Processing 610
Materials selection in mechanical design 500
Bounds for Statistical Estimation in Semiparametric Models 500
Forced degradation and stability indicating LC method for Letrozole: A stress testing guide 500
Ideology and Meaning-Making under the Putin Regime 450
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6478602
求助须知:如何正确求助?哪些是违规求助? 8280115
关于积分的说明 17659941
捐赠科研通 5561094
什么是DOI,文献DOI怎么找? 2911191
邀请新用户注册赠送积分活动 1888194
关于科研通互助平台的介绍 1742021