Amino acid synergetic effect on structure, morphology and surface properties of biomimetic apatite nanocrystals

Alanine, arginine and aspartic acid have been used as co-reagents during the synthesis of a biomimetic calcium-deficient hydroxyapatite (CDHA) for the synergistic coupling of synthesis and functionalization. The surface and bulk characterizations are consistent with a binding model in which the amin...

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Veröffentlicht in:Acta biomaterialia 2009-05, Vol.5 (4), p.1241-1252
Hauptverfasser: Palazzo, Barbara, Walsh, Dominic, Iafisco, Michele, Foresti, Elisabetta, Bertinetti, Luca, Martra, Gianmario, Bianchi, Claudia Letizia, Cappelletti, Giuseppe, Roveri, Norberto
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Sprache:eng
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Zusammenfassung:Alanine, arginine and aspartic acid have been used as co-reagents during the synthesis of a biomimetic calcium-deficient hydroxyapatite (CDHA) for the synergistic coupling of synthesis and functionalization. The surface and bulk characterizations are consistent with a binding model in which the amino acid is preferentially bound to the CDHA nanocrystal surface by its lateral chain group. The ζ-potential measurements show that the amino acid-functionalized CDHA surface charge shifts towards neutral compared to CDHA synthesized in the absence of amino acids. Amino acids bound to the crystal induce crystal growth inhibition predominantly at the Ca-rich surfaces during the initial stages of crystallization. Moreover, high-resolution transmission electron microscopy measurements suggest a model for needle-shaped CDHA nanocrystals formation in the presence of either arginine or aspartic acid based on the oriented aggregation of primary crystallite domains specifically along the c-axis direction and the self-assembly of preformed nanoparticles. The results have significant importance for the control of the shape, morphology and aggregation of the CDHA nanocrystals, while the observed surface modifications are of marked importance for the nature, stability and reactivity of the functionalized surfaces produced.
ISSN:1742-7061
1878-7568
DOI:10.1016/j.actbio.2008.10.024