The effect of proteoglycans of cartilage and over-sulphated polysaccharides on the development of calcium-hydroxy-apatite (CHA) crystal formation in vitro.

M Németh-Csóka, A Sárközi
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Abstract

A coulometric model system is described which facilitates the quantitative study of the kinetics of transformation of amorphous calcium phosphate (ACP) into calcium-hydroxy-apatite (CHA) crystals. Proteoglycans of high molecular weight and over-sulphated polysaccharides (Arteparon, dextran sulphate) delayed CHA crystal formation. The results have enabled us to characterize the structure activity relationship of inhibitors of CHA formation, and to postulate a general structural requirement for molecules with inhibitory effect. As working mechanism, binding of calcium ions by sulphate groups of polyanions was supposed, which might reversibly impair "the critical nuclei formation", and/or further deposition of calcium ions in the CHA crystals. The clinical, therapeutical significance of the determination of the threshold concentration of different compounds is discussed.

软骨蛋白聚糖和过硫酸盐多糖对体外钙羟基磷灰石(CHA)晶体形成的影响。
描述了一种库仑模型系统,该系统有助于定量研究无定形磷酸钙(ACP)向钙羟基磷灰石(CHA)晶体转变的动力学。高分子量的蛋白聚糖和过硫酸盐多糖(阿替帕龙、硫酸葡聚糖)延缓了CHA晶体的形成。这些结果使我们能够表征CHA形成抑制剂的结构活性关系,并假设具有抑制作用的分子的一般结构要求。据推测,钙离子与多阴离子的硫酸盐基团结合可能会可逆地破坏“临界核形成”,并/或钙离子在CHA晶体中的进一步沉积。讨论了测定不同化合物的阈值浓度的临床和治疗意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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