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Effects of Ti surface treatments with silane and arginylglycylaspartic acid peptide on bone cell progenitors

机译:硅烷和精氨酰基糖基天冬氨酸肽对钛表面处理对骨细胞祖细胞的影响

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Achieving optimal aesthetic appearance is a major objective in dental implant design, and the interaction between the materials and the bone cell progenitors is an important factor in the attainment of this objective. In this study, a novel concept was evaluated by varying the surface modifications on titanium (Ti). Different levels of roughness can be attained by machine grinding (M), sand blasting, and acid etching (SLA) of the samples. The behavior of bone cell progenitors (D1) on the surfaces of Ti disks with different surface modifications was investigated. The surfaces of M or SLA disks were silanized (MS or SLAS group) through treatment with silane/Gly-Arg-GlyAsp-Ser (GRGDS) peptide (MSP or SLASP group) and anchored particles of tetracalcium phosphate (TTCP) on the specimen surfaces (SLA-TTCP group). Physicochemical analysis was performed by metallographic microscopy, scanning electron microscopy, and contact angle analysis. The proliferation and the quantitative alkaline phosphatase (ALP) production of D1 cells on the surface of different sample groups were determined. The SLASP group had a significantly larger D1 cell proliferation than the other groups after 4 and 7 d of incubation (p < 0.05). ALP expression was a very early marker of differentiation, and was the first indication of the increasing number of cells at 7 d of culture. Among the groups in the M substrate series (i.e., M, MS, and MSP) and in the SLA series (i.e., SLA, SLAS, and SLASP), the MSP and SLASP specimens exhibited superior differentiation abilities on respective cultures until day 7 and day 10. A high number of hydrophilic surfaces dominated cell proliferation in the early stage of cell attachment. However, factors affecting the pore structure and the surface morphology can improve cell proliferation and differentiation. According to analyses of proliferation and ALP expression of bone cell progenitors D1, the original SLA implant surface can be improved with surface treatment methods, such as silanization and treatment with graft GRGDS pentapeptide. These methods can be potential candidates for the promotion of bone growth.
机译:实现最佳的美学外观是牙科植入物设计的主要目标,而材料与骨细胞祖细胞之间的相互作用是实现该目标的重要因素。在这项研究中,通过改变钛(Ti)的表面改性来评估一种新颖的概念。可以通过机器研磨(M),喷砂和酸蚀刻(SLA)获得不同程度的粗糙度。研究了具有不同表面修饰的Ti盘表面上骨细胞祖细胞(D1)的行为。通过用硅烷/ Gly-Arg-GlyAsp-Ser(GRGDS)肽(MSP或SLASP组)和磷酸四钙(TTCP)固定的颗粒处理,对M或SLA圆盘的表面进行硅烷化处理(MS或SLAS组) (SLA-TTCP组)。通过金相显微镜,扫描电子显微镜和接触角分析进行理化分析。测定不同样品组表面上D1细胞的增殖和定量碱性磷酸酶(ALP)产生。孵育4天和7天后,SLASP组的D1细胞增殖明显高于其他组(p <0.05)。 ALP表达是分化的非常早期的标志,并且是培养7天时细胞数量增加的第一个迹象。在M底物系列(即M,MS和MSP)和SLA系列(即SLA,SLAS和SLASP)的组中,MSP和SLASP样品在各自的培养物中均显示出优异的分化能力,直到第7天和第10天。在细胞附着的早期阶段,大量的亲水性表面主导着细胞的增殖。但是,影响孔结构和表面形态的因素可以改善细胞增殖和分化。根据对骨细胞祖细胞D1的增殖和ALP表达的分析,可以通过表面处理方法(例如硅烷化和移植GRGDS五肽处理)改善原始SLA植入物表面。这些方法可能是促进骨生长的潜在候选方法。

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