Eliades G, Palaghias G, Vougiouklakis G
Research Center for Biomaterials, Athens, Greece.
Dent Mater. 1997 Jan;13(1):24-33. doi: 10.1016/s0109-5641(97)80005-x.
The aim of the study was to evaluate the effect of some acidic conditioners on dentin morphology, molecular composition and collagen conformation in situ.
Smear layer-covered dentin specimens prepared from third molars immediately after extraction were imaged by tapping made AFM and analyzed by MIR-FTIR spectroscopy. The same specimens were subjected to conditioning treatments with CA Agent (Kuraray), Scotchbond Etchant (3M Dental Products) and Scotchbond MP Etchant (3M Dental Products) gels and then imaged and analyzed again. The extent of dentin decalcification at the uppermost 2 microns region was calculated from the percentage reduction in the-PO4/amide I peak area ratio of conditioned specimens relative to their individual smear layer-covered references. These results were compared by ANOVA and Scheffé statistical analyses. The conformational changes of dentin type I collagen at the region were studied qualitatively by deconvoluting the amide I bands of MIR-FTIR spectra and assigning the band components to carbonyl hydrogen bonding states related to the alpha-helix structure.
All the conditioners removed the smear layer, funneled the tubules, increased the intertubular roughness and contaminated the dentin surfaces with residues from irreversibly adsorbed thickening agents. Conditioned dentin surfaces showed a reduction in orthophosphates and carbonates and an increase in amide I, II and III groups. CA Agent manifested a significantly lower extent of dentin decalcification than Scotchbond etchants (p < 0.05). Collagen conformational changes involved a decrease in intermolecular hydrogen bonded amide I carbonyls associated with the alpha-helix structure and enhancement of imide carbonyls hydrogen bonded to water, which suggest collagen denaturation.
Apart from dentin decalcification, the acidic conditioners induced considerable changes on dentin collagen conformation mostly associated with denaturation processes. In addition, irreversibly adsorbed residual thickeners substantially modified the morphology and composition of dentin surfaces. These findings show the complex interaction pathways between conditioners and dentin surfaces and the great potential of modern in situ imaging and analysis techniques in probing these interactions.
本研究旨在评估某些酸性调节剂对牙本质形态、分子组成及原位胶原构象的影响。
从拔除的第三磨牙制备的涂有玷污层的牙本质标本,在拔除后立即用轻敲模式原子力显微镜成像,并用中红外傅里叶变换红外光谱法进行分析。对相同的标本用CA试剂(可乐丽公司)、Scotchbond酸蚀剂(3M牙科产品公司)和Scotchbond MP酸蚀剂(3M牙科产品公司)凝胶进行调节处理,然后再次成像和分析。根据调节标本相对于其各自涂有玷污层的对照的 -PO4/酰胺I峰面积比的降低百分比,计算最上层2微米区域的牙本质脱钙程度。通过方差分析和谢费统计分析对这些结果进行比较。通过对中红外傅里叶变换红外光谱的酰胺I带进行去卷积,并将带成分分配给与α - 螺旋结构相关的羰基氢键状态,定性研究该区域牙本质I型胶原的构象变化。
所有调节剂均去除了玷污层,使牙本质小管呈漏斗状,增加了小管间粗糙度,并用不可逆吸附的增稠剂残留物污染了牙本质表面。经调节的牙本质表面显示正磷酸盐和碳酸盐减少,酰胺I、II和III基团增加。CA试剂表现出的牙本质脱钙程度明显低于Scotchbond酸蚀剂(p < 0.05)。胶原构象变化包括与α - 螺旋结构相关的分子间氢键结合的酰胺I羰基减少,以及与水氢键结合的酰亚胺羰基增强,这表明胶原变性。
除牙本质脱钙外,酸性调节剂还引起牙本质胶原构象的显著变化,这些变化大多与变性过程有关。此外,不可逆吸附的残留增稠剂极大地改变了牙本质表面的形态和组成。这些发现揭示了调节剂与牙本质表面之间复杂的相互作用途径,以及现代原位成像和分析技术在探究这些相互作用方面的巨大潜力。