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INTERACTION OF SODIUM POLYACRYLATE WITH OCTACALCIUM PHOSPHATE

机译:聚丙烯酸钠与磷酸钙的相互作用

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NaPA inhibits nucleation and growth of OCP, as well as its hydrolysis into HA. The first of the two phenomena is clearly due to a nonspecific interaction, as indicated by the lack of any significative adsorption of the polyelectrolyte on OCP crystals and by the isotropic reduction of the coherence lengths of the perfect crystalline domains on increasing polymer concentration in solution. On the other hand, the inhibition of OCP crystals. We verified that, in similar conditions, the adsorption of NaPA on HA crystals reaches a maximum relative amount of 2 wt%, in agreement with previous studies about NaPA adsorption on HA. The polymer preference for OCP structure is confirmed by the comparison among the different crystal habits of HA crystals obtained by hydrolysis at different NaPA concentrations. The crystals obtained in 10~(-2) mM NaPA, that is when just a partial hydrolysis occurs, exhibit a morphology quite similar to that of HA crystals obtained by hydrolysis in water, whereas those obtained in 10~(-3) mM NaPA are clearly affected by the polymer. This finding suggests that when the polyelectrolyte can choose, as in partially hydrolyzed material, it is preferentially adsorbed on OCP rather than on HA crystals. On the basis of the structure of OCP and HA, it must be supposed that the preference of the polyelectrolyte for OCP is due to the presence of the hydrated layer, where it is adsorbed on the (100) face causing an anisotropic variation of the coherence lengths. The morphology of HA crystals obtained by OCP hydrolysis is very similar to that of the plate-like crystals of bone and dentine, and supports the hypothesis of an OCP involvement in the biomineralization process of these tissues. The adsorption on the hydrated layer of the (100) face prevents OCP hydrolysis into HA, in agreement with the hypothesis that hydrolysis takes place along this face, as suggested to explain the contemporary presence of OCP and HA in the same crystal of calcifying dentine. Although these results cannot be extrapolated to in vivo interaction between acidic proteins and calcium phosphates, they point out the important role that the presence of acidic macromolecules can play on the relative stability of octacalcium phosphate and hydroxyapatite, as well as on the shape, dimensions and crystallinity of the final crystals.
机译:NaPA抑制OCP的成核和生长,以及其水解成HA的能力。两种现象中的第一种显然是由于非特异性相互作用所致,这是由于聚电解质在OCP晶体上缺乏任何明显的吸附以及随着溶液中聚合物浓度的增加各向同性地降低了完美晶域的相干长度。另一方面,抑制了OCP晶体。我们证实,在类似条件下,NaPA在HA晶体上的吸附达到2 wt%的最大相对量,这与先前有关NaPA在HA上吸附的研究一致。通过在不同NaPA浓度下水解获得的HA晶体的不同晶体习性之间的比较,可以确定聚合物对OCP结构的偏爱。在10〜(-2)mM NaPA中获得的晶体,即仅发生部分水解时,其形态与在水中水解获得的HA晶体的形态非常相似,而在10〜(-3)mM NaPA中获得的HA晶体的形态十分相似。显然受聚合物影响。这一发现表明,当聚电解质可以选择时,如在部分水解的材料中一样,它优先吸附在OCP而不是HA晶体上。根据OCP和HA的结构,必须假定聚电解质对OCP的偏爱是由于存在水合层,该水合层吸附在(100)面上,导致相干性各向异性变化长度。通过OCP水解获得的HA晶体的形态与骨骼和牙本质的板状晶体的形态非常相似,并支持OCP参与这些组织的生物矿化过程的假设。 (100)面的水合层上的吸附可防止OCP水解为HA,这与假说是沿该面发生水解的假设相吻合,这可以解释OCP和HA在同一钙化牙本质晶体中的存在。尽管这些结果不能外推至酸性蛋白质和磷酸钙之间的体内相互作用,但它们指出酸性大分子的存在对磷酸八钙和羟基磷灰石的相对稳定性以及形状,尺寸和结构具有重要作用。最终晶体的结晶度。

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