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添加剂通过协同离子缔合过程影响碳酸钙溶液的相行为。

Additives influence the phase behavior of calcium carbonate solution by a cooperative ion-association process.

作者信息

Zou Zhaoyong, Polishchuk Iryna, Bertinetti Luca, Pokroy Boaz, Politi Yael, Fratzl Peter, Habraken Wouter J E M

机构信息

Max Planck Institute of Colloids and Interfaces, Department of Biomaterials, Potsdam, Germany.

出版信息

J Mater Chem B. 2018 Jan 21;6(3):449-457. doi: 10.1039/c7tb03170j. Epub 2018 Jan 2.

Abstract

Amorphous calcium carbonate (ACC) has been widely found in biomineralization, both as a transient precursor and a stable phase, but how organisms accurately control its formation and crystallization pathway remains unclear. Here, we aim to illuminate the role of biologically relevant additives on the phase behaviour of calcium carbonate solution by investigating their effects on the formation of ACC. Results show that divalent cations like magnesium (Mg) ions and negatively charged small organic molecules like aspartic acid (Asp) have little/no effect on ACC formation. However, the particle size of ACC is significantly reduced by poly(aspartic acid) (pAsp) with long chain-length, but no effect on the position of the phase boundary for ACC formation was observed. Phosphate (PO ) ions are even more effective in reducing ACC particle size, and shift the phase boundary for ACC formation to lower concentrations. These phenomena can be explained by a cooperative ion-association process where the formation of ACC is only influenced by additives that are able to attract either Ca ions or CO ions and, more importantly, introduce an additional long range interaction between the CaCO complexes and promote the phase separation process. The findings corroborate with our proposed model of ACC formation via spinodal decomposition and provide a more realistic representation of how biology can direct mineralization processes.

摘要

无定形碳酸钙(ACC)在生物矿化过程中广泛存在,既是一种过渡前体,也是一种稳定相,但生物体如何精确控制其形成和结晶途径仍不清楚。在此,我们旨在通过研究生物相关添加剂对ACC形成的影响,阐明其对碳酸钙溶液相行为的作用。结果表明,二价阳离子如镁(Mg)离子和带负电荷的小分子如天冬氨酸(Asp)对ACC形成几乎没有/没有影响。然而,长链聚天冬氨酸(pAsp)可显著减小ACC的粒径,但未观察到其对ACC形成相界位置的影响。磷酸根(PO)离子在减小ACC粒径方面更有效,并将ACC形成的相界移至更低浓度。这些现象可以通过协同离子缔合过程来解释,其中ACC的形成仅受能够吸引钙离子或碳酸根离子的添加剂影响,更重要的是,在碳酸钙络合物之间引入额外的长程相互作用并促进相分离过程。这些发现与我们提出的通过旋节线分解形成ACC的模型相一致,并为生物学如何指导矿化过程提供了更现实的描述。

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