Biomimetic Mineralization of CaCO3on a Phospholipid Monolayer: From an Amorphous Calcium Carbonate Precursor to Calcite via Vaterite

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Titel: Biomimetic Mineralization of CaCO3on a Phospholipid Monolayer: From an Amorphous Calcium Carbonate Precursor to Calcite via Vaterite
Autoren: Xiao, Junwu, Wang, Zhining, Tang, Yecang, Yang, Shihe
Quelle: Langmuir. 26:4977-4983
Verlagsinformationen: American Chemical Society (ACS), 2009.
Publikationsjahr: 2009
Schlagwörter: Microscopy, Spectrum Analysis, Atomic Force, 02 engineering and technology, Models, Theoretical, Microscopy, Atomic Force, Spectrum Analysis, Raman, Electron, 01 natural sciences, Calcium Carbonate, 0104 chemical sciences, Calcium Carbonate: chemistry, Theoretical, Microscopy, Electron, Transmission, X-Ray Diffraction, Models, Biomimetics, Phospholipids: chemistry, Microscopy, Electron, Scanning, Transmission, Scanning, 0210 nano-technology, Raman, Phospholipids
Beschreibung: A phospholipid monolayer, approximately half the bilayer structure of a biological membrane, can be regarded as an ideal model for investigating biomineralization on biological membranes. In this work on the biomimetic mineralization of CaCO(3) under a phospholipid monolayer, we show the initial heterogeneous nucleation of amorphous calcium carbonate precursor (ACC) nanoparticles at the air-water interface, their subsequent transformation into the metastable vaterite phase instead of the most thermodynamically stable calcite phase, and the ultimate phase transformation to calcite. Furthermore, the spontaneity of the transformation from vaterite to calcite was found to be closely related to the surface tension; high surface pressure could inhibit the process, highlighting the determinant of surface energy. To understand better the mechanisms for ACC formation and the transformation from ACC to vaterite and to calcite, in situ Brewster angle microscopy (BAM), ex situ scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and X-ray diffraction analysis were employed. This work has clarified the crystallization process of calcium carbonate under phospholipid monolayers and therefore may further our understanding of the biomineralization processes induced by cellular membranes.
Publikationsart: Article
Sprache: English
ISSN: 1520-5827
0743-7463
DOI: 10.1021/la903641k
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/19911801
https://pubmed.ncbi.nlm.nih.gov/19911801/
https://pubs.acs.org/doi/10.1021/la903641k
http://repository.ust.hk/ir/Record/1783.1-30089
https://core.ac.uk/display/34025952
https://www.ncbi.nlm.nih.gov/pubmed/19911801
http://europepmc.org/abstract/MED/19911801
Dokumentencode: edsair.doi.dedup.....e672ad0b4a41bbbdba35b8eb46be685d
Datenbank: OpenAIRE
Beschreibung
Abstract:A phospholipid monolayer, approximately half the bilayer structure of a biological membrane, can be regarded as an ideal model for investigating biomineralization on biological membranes. In this work on the biomimetic mineralization of CaCO(3) under a phospholipid monolayer, we show the initial heterogeneous nucleation of amorphous calcium carbonate precursor (ACC) nanoparticles at the air-water interface, their subsequent transformation into the metastable vaterite phase instead of the most thermodynamically stable calcite phase, and the ultimate phase transformation to calcite. Furthermore, the spontaneity of the transformation from vaterite to calcite was found to be closely related to the surface tension; high surface pressure could inhibit the process, highlighting the determinant of surface energy. To understand better the mechanisms for ACC formation and the transformation from ACC to vaterite and to calcite, in situ Brewster angle microscopy (BAM), ex situ scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and X-ray diffraction analysis were employed. This work has clarified the crystallization process of calcium carbonate under phospholipid monolayers and therefore may further our understanding of the biomineralization processes induced by cellular membranes.
ISSN:15205827
07437463
DOI:10.1021/la903641k