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The effect of chemical structure of carboxylate molecules on hydroxyapatite nanoparticles. A structural and morphological study

机译:羧酸盐分子化学结构对羟基磷灰石纳米颗粒的影响。结构和形态学研究

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摘要

Being the most abundant non-macromolecular organic component of bone, the role of citrate (Cit) in hydroxyapatite (HA) crystallization is of high relevance. In this work we have investigated the influence of hydroxycitrate (CitOH) and glutarate (Glr) on HA crystallization in terms of particle growth, composition, and morphology in comparison to Cit. CitOH and Glr have been selected for this work because they share the same backbone structure of Cit but bear different functional groups in the central region. Our data has revealed that CitOH strongly inhibits HA crystallization more efficiently than Cit. CitOH-HA nanoparticles are composed of platy, elongated particles similar to those of Cit-HA but they are ca. twice smaller and have a lower crystal order. On the other hand, Glr does not inhibit HA crystallization as Cit, but leads to the formation of OCP platelets that convert with maturation time to HA nanorods with larger aspect ratio than Cit-HA. In comparison to Cit-HA samples, Glr-HA nanoparticles have bigger dimensions, and higher structural order. Overall, our data reveal that the central carboxyl group of Cit is involved in the selective binding with HA crystal surface and in regulating HA crystal growth. The results of this work highlight new possibilities to control the formation of HA for designing advanced bioactive materials and give new insights on the role of the structure of Cit in regulating the HA morphology.
机译:作为骨骼最丰富的非大分子有机成分,柠檬酸盐(CIT)在羟基磷灰石(HA)结晶中的作用具有高相关性。在这项工作中,我们研究了与CIT比较的颗粒生长,组成和形态方面对羟基柠檬酸酯(CITOH)和戊二酸盐(GLR)对HA结晶的影响。为这项工作选择了Citoh和GLR,因为它们共享了CIT的相同骨干结构,但在中部地区承担不同的功能群体。我们的数据透露,Citoh强烈地抑制了高效的疾病比Cit更有效。 CaCtOH-HA纳米粒子由Platy,细长颗粒组成,细长颗粒类似于Cit-Ha,但它们是Ca。两倍较小,晶莹状顺序较低。另一方面,GLR不会抑制HA结晶作为CIT,但导致ocp血小板的形成,该血小板与较大宽高比的纵横比的成熟时间转化为HA纳米镜。与Cit-HA样品相比,GLR-HA纳米颗粒具有更大的尺寸和更高的结构序列。总体而言,我们的数据表明,CIT的中央羧基参与与HA晶体表面的选择性结合和调节HA晶体生长。这项工作的结果突出了控制HA的形成,以设计高级生物活性材料,并对CIT结构的作用进行新的洞察监管HA形态。

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