Chen Ping-Ju, Hsieh Jung-Pei, Chang Hsiao-Tzu, Chen Yuh-Ling, Chuang Shu-Fen
Department of Dentistry, Changhua Christian Hospital, Changhua 50006, Taiwan.
School of Dentistry and Institute of Oral Medicine, College of Medicine, National Cheng Kung University, Tainan 70101, Taiwan.
J Funct Biomater. 2025 Jan 3;16(1):11. doi: 10.3390/jfb16010011.
Recently, photoactivated riboflavin (RF) treatments have been approved to improve resin-dentin bonding by enhancing dentinal collagen crosslinking. This study aimed to evaluate whether RF activated by blue light (BL, 450 nm) strengthens the collagen matrix, increases resistance to enzymatic degradation, and improves adhesion as effectively as ultraviolet A (UVA, 375 nm) activation. Six groups were examined: control (no treatment); RF0.1UV2 (0.1% RF with 2 min of UVA irradiation); RF0.1BL1, RF0.1BL2, RF1BL1, and RF1BL2 (0.1% and 1% RF with 1 or 2 min of BL irradiation). The effects of RF/BL on collagen crosslinking were validated by gel electrophoresis. A nanoindentation test showed that both RF/UVA and RF/BL treatments enhanced the elastic modulus and nanohardness of demineralized dentin. A zymography assay using collagen extracted from demineralized dentin also revealed significant matrix metalloproteinase-2 inhibition across all RF treatments. Microtensile bond strength (µTBS) tests conducted both post-treatment and after 7-day enzymatic degradation showed that three RF0.1 groups (RF0.1UV2, RF0.1BL1, and RF0.1BL2) maintained high µTBS values after degradation, while RF0.1BL1 generated a significantly thicker hybrid layer compared to other groups. These findings suggest that RF/BL is as effective as RF/UVA in crosslinking dentinal collagen and resisting enzymatic degradation, with 0.1% RF proving superior to 1% RF in enhancing dentin bonding.
最近,光活化核黄素(RF)治疗已被批准用于通过增强牙本质胶原蛋白交联来改善树脂与牙本质的粘结。本研究旨在评估蓝光(BL,450nm)激活的RF是否能像紫外线A(UVA,375nm)激活一样有效地强化胶原蛋白基质、提高对酶降解的抵抗力并改善粘结力。研究了六组:对照组(未处理);RF0.1UV2(0.1%RF,照射UVA 2分钟);RF0.1BL1、RF0.1BL2、RF1BL1和RF1BL2(0.1%和1%RF,照射BL 1或2分钟)。通过凝胶电泳验证了RF/BL对胶原蛋白交联的影响。纳米压痕试验表明,RF/UVA和RF/BL处理均提高了脱矿牙本质的弹性模量和纳米硬度。使用从脱矿牙本质中提取的胶原蛋白进行的酶谱分析也显示,所有RF处理均显著抑制基质金属蛋白酶-2。在处理后和7天酶降解后进行的微拉伸粘结强度(µTBS)测试表明,三个RF0.1组(RF0.1UV2、RF0.1BL1和RF0.1BL2)在降解后保持较高的µTBS值,而RF0.1BL1与其他组相比产生了明显更厚的混合层。这些发现表明,RF/BL在交联牙本质胶原蛋白和抵抗酶降解方面与RF/UVA一样有效,0.1%RF在增强牙本质粘结方面优于1%RF。