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Experimental use of an acrolein-based primer as collagen cross-linker for dentine bonding

机译:基于丙烯醛的底漆的实验性用作牙本质键合的胶原蛋白交联剂

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Abstract Objectives The objective of the present study was to investigate the long-term effect of 0.01% acrolein (ACR) aqueous solution, employed as an additional primer, on the mechanical durability and enzymatic activity of resin-dentine interfaces created with a simplified etch-and-rinse adhesive. Methods Dentine surfaces were etched with 35% phosphoric acid for 15s, rinsed and blot-dried. Specimens were then assigned to: Group 1: dentine pre-treated with 0.01% ACR aqueous solution for 1min and bonded with Adper Scotchbond 1 XT (SB1XT), a 2-step etch-and-rinse adhesive; Group 2: SB1XT was applied on untreated acid-etched dentine (control). Resin composite build-ups were made using Filtek Z250. Microtensile bond strength was tested by stressing sectioned specimens to failure immediately or after 1year of storage in artificial saliva at 37°C. Zymography and in-situ zymography assays were performed for examining dentine matrix metalloproteinase (MMP) activities. Results The use of 0.01% ACR as conditioning primer appeared to have contributed better to preservation of bond strength over time without affecting immediate bond strength. Zymography and in-situ zymography showed reduction in MMP activities after the application of ACR. Conclusion Dentine collagen cross-linking produced by an ACR-based primer increases the longevity of resin-dentine bonds by reinforcement of the adhesive interface and reduction of dentine MMP activities. Further studies are required to evaluate the potential in vivo and in vivo cytotoxicity of ACR. Clinical significance The acrolein-based primer is a potentially useful clinical bonding tool because it demonstrates good collagen cross-linking ability within a clinically-acceptable working time. Although a low ACR concentration was employed in the present study, the cytotoxicity of ACR should be tested prior to clinical use.
机译:摘要目的本研究的目的是研究用简化蚀刻产生的树脂牙本质界面的机械耐久性和酶促活性的0.01%丙烯醛(ACR)水溶液的长期效果。和冲洗粘合剂。方法用35%磷酸蚀刻牙本质表面15s,冲洗并呈污渍干燥。然后将标本分配给:第1组:用0.01%ACR水溶液预处理的牙本质,并用吸附剂透明质1 XT(SB1XT),2步蚀刻和冲洗粘合剂粘合;第2组:将SB1XT应用于未处理的酸蚀刻牙本质(对照)。使用FILTEK Z250进行树脂复合堆积。通过在37℃下将折叠的样品造成折叠试样或在1℃的人工唾液中储存后的储存来测试微调粘合强度。进行酶沉积和原位酶测定,用于检查牙本质基质金属蛋白酶(MMP)活性。结果使用0.01%ACR作为调理引物的用途似乎在不影响立即粘合强度的情况下促使粘合强度的保存更好。酶谱和原位酶谱表明ACR施用后的MMP活性降低。结论通过增强粘合剂界面和牙本质MMP活性的增强,通过增强树脂引物产生的牙齿胶原交联增加树脂牙接键的寿命。需要进一步的研究来评估Vivo的潜力和ACR的体内细胞毒性。临床意义基于丙烯醛的底漆是一种潜在有用的临床结合工具,因为它在临床上可接受的工作时间内证明了良好的胶原交联能力。尽管在本研究中使用了低ACR浓度,但在临床用途之前应该测试ACR的细胞毒性。

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