核黄素-超紫外-A 胶原交联疗法在改善牙本质粘合力和抗酶消化能力方面的作用。

IF 3.4 3区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Journal of Dental Sciences Pub Date : 2025-01-01 Epub Date: 2024-10-05 DOI:10.1016/j.jds.2024.09.022
Yung-Show Chiang, Ping-Ju Chen, Chun-Chan Ting, Yuh-Ling Chen, Shu-Fen Chuang
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引用次数: 0

摘要

背景/目的:核黄素-紫外线-A(RF-UVA)治疗在交联胶原和改善牙本质粘接方面的功效已得到证实。然而,混合层的生物降解可能会影响粘接效果。本研究的目的是评估不同的射频-紫外线-A(RF-UVA)处理方法在保护牙本质粘接不受酶消化方面的能力:通过凝胶电泳(SDS-PAGE)对经过不同射频(0.1 %、1 %)-UVA(1、2、5 分钟)处理和 5 % 戊二醛(GA)处理的胶原蛋白进行检查,不含或含酶消化。用三种 RF-UVA 处理方法(0.1%RF/1-minUVA、0.1%RF/2-minUVA 和 1%RF/1-minUVA)之一、GA 或蒸馏水对 25 颗牙本质暴露的牙齿进行酸蚀处理,然后用粘合剂和树脂复合材料进行修复。存放 24 小时后,将这些牙齿切成微梁。其中一半接受早期微拉伸粘接强度(μTBS)测试,另一半在测试前在酶溶液中存放 7 天。用 TEM 对纳米渗漏和杂化层降解情况进行了检测:根据 SDS-PAGE 结果,所有组的胶原蛋白在消化后都出现了强烈的 γ 带消散。对于早期粘合试样和酶解后试样,0.1%RF/2-minUVA 处理组的 μTBS 最高,且无过早失效现象。其 TEM 图像显示,消化后的纳米渗漏较少,这归功于混合层中胶原纤维的良好悬浮和树脂渗透:结论:RF-UVA 处理具有胶原交联效果,可改善树脂与牙本质的粘接。0.1 %RF/2-minUVA通过优化扩展牙本质胶原基质以促进混合层的形成,有效提高了牙本质粘接强度和抗酶消化能力。
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Riboflavin-ultraviolet-A collagen crosslinking treatments in improving dentin bonding and resistance to enzymatic digestion.

Background/purpose: The efficacy of riboflavin-ultraviolet-A (RF-UVA) treatment in crosslinking collagen and improving dentin bonding has been proven. However, biodegradation of the hybrid layer may compromise the bonding. The purpose of this study was to evaluate different RF-UVA treatments regarding their ability to preserve dentin bonding from enzymatic digestion.

Materials and methods: Collagen subjected to different RF (0.1 %, 1 %)-UVA (1, 2, 5 min) treatments and 5 % glutaraldehyde (GA), without or with enzymatic digestion, were examined by gel electrophoresis (SDS-PAGE). Twenty-five teeth with exposed dentin were primed with one of three RF-UVA treatments (0.1 %RF/1-minUVA, 0.1 %RF/2-minUVA, and 1 %RF/1-minUVA), GA, or distilled water after acid-etching, then restored with an adhesive and a resin composite. After 24-h storage, these teeth were sectioned into microbeams. Half of them received an early microtensile bond strength (μTBS) test, while the other half was stored in enzyme solution for 7 days before testing. Nanoleakage and hybrid layer degradation were examined by TEM.

Results: According to SDS-PAGE results, all groups showed the dissipation of intense γ bands of collagen after digestion. For the early bonded specimens and after enzymatic digestions, 0.1 %RF/2-minUVA treated group presented the highest μTBS and none of premature failure. Its TEM images showed less nanoleakage after digestion, which is contributed to the well suspended collagen fibrils and resin infiltration in the hybrid layer.

Conclusion: RF-UVA treatment attained collagen crosslinking effects to improve resin-dentin bonding. 0.1 %RF/2-minUVA effectively enhanced dentin bond strength and resistance to enzymatic digestion by optimally expanding dentinal collagen matrix to facilitate hybrid layer formation.

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来源期刊
Journal of Dental Sciences
Journal of Dental Sciences 医学-牙科与口腔外科
CiteScore
5.10
自引率
14.30%
发文量
348
审稿时长
6 days
期刊介绍: he Journal of Dental Sciences (JDS), published quarterly, is the official and open access publication of the Association for Dental Sciences of the Republic of China (ADS-ROC). The precedent journal of the JDS is the Chinese Dental Journal (CDJ) which had already been covered by MEDLINE in 1988. As the CDJ continued to prove its importance in the region, the ADS-ROC decided to move to the international community by publishing an English journal. Hence, the birth of the JDS in 2006. The JDS is indexed in the SCI Expanded since 2008. It is also indexed in Scopus, and EMCare, ScienceDirect, SIIC Data Bases. The topics covered by the JDS include all fields of basic and clinical dentistry. Some manuscripts focusing on the study of certain endemic diseases such as dental caries and periodontal diseases in particular regions of any country as well as oral pre-cancers, oral cancers, and oral submucous fibrosis related to betel nut chewing habit are also considered for publication. Besides, the JDS also publishes articles about the efficacy of a new treatment modality on oral verrucous hyperplasia or early oral squamous cell carcinoma.
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