Faculty of Chemistry, Institute of Biological Chemistry, University Vienna, Währinger Str. 38, 1090 Vienna, Austria.
Sorbonne Université, CNRS, Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP), 4, Place Jussieu, F-75005 Paris, France.
Anal Chem. 2021 Jul 27;93(29):10204-10211. doi: 10.1021/acs.analchem.1c01561. Epub 2021 Jul 12.
Simulated body fluids (SBFs) that mimic human blood plasma are widely used media for studies in an extensive array of research fields, from biomineralization to surface and corrosion sciences. We show that these solutions undergo dynamic nanoscopic conformational rearrangements on the timescale of minutes to hours, even though they are commonly considered stable or metastable. In particular, we find and characterize nanoscale inhomogeneities made of calcium phosphate (CaP) aggregates that emerge from homogeneous SBFs within a few hours and evolve into prenucleation species (PNS) that act as precursors in CaP crystallization processes. These ionic clusters consist of ∼2 nm large spherical building units that can aggregate into suprastructures with sizes of over 200 nm. We show that the residence times of phosphate ions in the PNS depend critically on the total PNS surface. These findings are particularly relevant for understanding nonclassical crystallization phenomena, in which PNS are assumed to act as building blocks for the final crystal structure.
模拟体液 (SBF) 模拟人体血浆,被广泛应用于从生物矿化到表面和腐蚀科学等众多研究领域的研究中。我们表明,尽管这些溶液通常被认为是稳定或亚稳的,但它们在数分钟到数小时的时间尺度上会经历动态的纳米级构象重排。具体来说,我们发现并表征了由磷酸钙 (CaP) 聚集体组成的纳米级不均匀性,这些聚集体在数小时内从均匀的 SBF 中出现,并演变成成核前物质 (PNS),作为 CaP 结晶过程中的前体。这些离子簇由约 2nm 大小的球形构建单元组成,这些构建单元可以聚集形成超过 200nm 的超结构。我们表明,磷酸盐离子在 PNS 中的停留时间与 PNS 的总表面积密切相关。这些发现对于理解非经典结晶现象尤为重要,因为 PNS 被认为是最终晶体结构的构建块。