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含原花青素的磷酸提高了树脂/牙本质界面的结合稳定性。

Phosphoric acid containing proanthocyanidin enhances bond stability of resin/dentin interface.

机构信息

Departmento de Odontologia Restauradora, Faculdade de Odontologia de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brazil.

Department of Restorative Dentistry, Faculty of Dentistry, University of Manitoba, Winnipeg, MB, Canada.

出版信息

Braz Dent J. 2022 Jul-Aug;33(4):62-70. doi: 10.1590/0103-6440202203941.

Abstract

Proanthocyanidin (PA) is a promising dentin biomodifier due to its ability to stabilize collagen fibrils against degradation by matrix metalloproteinases (MMPs); however, the most effective protocol to incorporate PA into bonding procedures is still unclear. This study evaluated the effect of dentin biomodification with a PA acid etchant on MMP activity, adhesive interface morphology and resin-dentin microtensile bond strength. Sound extracted human molars were flattened to expose dentin and acid-etched for 15 s according to the groups: EXP - experimental phosphoric acid; EXP+PA - experimental phosphoric acid 10% PA; TE - total-etching system; SE - self-etching system. Samples were restored with composite resin and stored in distilled water (37ºC). MMP activity and interface morphology were analyzed after 24 h by in situ zymography (n=6) and scanning electron microscopy (n=3), respectively. The resin-dentin microtensile bond strength (μTBS) was evaluated after 24 h and 6 months storage (n=6). Significantly higher MMP activity was detected in etched dentin compared with untreated dentin (p<0.05), but no difference among acid groups was found. Resin tags and microtags, indicative of proper adhesive system penetration in dentinal tubules and microtubules, were observed along the hybrid layer in all groups. There was no difference in μTBS between 24 h and 6 months for EXP+PA; moreover, it showed higher long-term μTBS compared with TE and EXP (p<0.05). The results suggest that 15 s of biomodification was not sufficient to significantly reduce MMP activity; nonetheless, EXP+PA was still able to improve resin-dentin bond stability compared with total- and self-etching commercial systems.

摘要

原花青素(PA)是一种有前途的牙本质生物调节剂,因为它能够稳定胶原蛋白纤维,防止基质金属蛋白酶(MMPs)降解;然而,将 PA 纳入粘接程序的最有效方案仍不清楚。本研究评估了 PA 酸蚀刻剂对 MMP 活性、黏附界面形态和树脂-牙本质微拉伸黏结强度的牙本质生物改性效果。将提取的健康人磨牙磨平,暴露牙本质,根据以下组别用酸蚀刻 15s:EXP-实验性磷酸;EXP+PA-实验性磷酸 10%PA;TE-全酸蚀系统;SE-自酸蚀系统。用复合树脂修复样本,并储存在蒸馏水中(37°C)。24 h 后通过原位酶谱分析(n=6)和扫描电子显微镜(n=3)分别分析 MMP 活性和黏附界面形态。24 h 和 6 个月储存后(n=6)评估树脂-牙本质微拉伸黏结强度(μTBS)。与未处理牙本质相比,蚀刻牙本质中 MMP 活性明显升高(p<0.05),但酸组之间无差异。在所有组中,在混合层中均观察到树脂标签和微标签,表明适当的黏附系统渗透到牙本质小管和微管中。EXP+PA 在 24 h 和 6 个月之间的 μTBS 没有差异;此外,与 TE 和 EXP 相比,它显示出更高的长期 μTBS(p<0.05)。结果表明,15s 的生物改性不足以显著降低 MMP 活性;尽管如此,与全酸蚀和自酸蚀商业系统相比,EXP+PA 仍能提高树脂-牙本质黏结稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1db8/9645179/18c68f11cc7c/1806-4760-bdj-33-04-62-gch1.jpg

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