SYNTHESIS AND CHARACTERISATION OF AMINO ACID-FUNCTIONALISED HYDROXYAPATITE NANORODS

Aqueous colloids of amino acid-functionalised hydroxyapatite (HAP; Ca10(PO4)6(OH)2) nanoparticles with rod-like morphology and uniform size were prepared by hydrothermal crystallisation at 80 C and pH 9 in highly supersaturated solutions with a Ca2+:amino acid molar ratio of 1:2. Stable suspensions...

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Veröffentlicht in:Journal of materials chemistry 2004-01, Vol.14 (14), p.2277-2281
Hauptverfasser: Gonzalez-McQuire, R, Chane-Ching, J-Y, Vignaud, E, Lebugle, A, Mann, S
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Chane-Ching, J-Y
Vignaud, E
Lebugle, A
Mann, S
description Aqueous colloids of amino acid-functionalised hydroxyapatite (HAP; Ca10(PO4)6(OH)2) nanoparticles with rod-like morphology and uniform size were prepared by hydrothermal crystallisation at 80 C and pH 9 in highly supersaturated solutions with a Ca2+:amino acid molar ratio of 1:2. Stable suspensions of positively charged nanorods, < 80 nm in length and about 5 nm in width, were obtained in the presence of glycine, alanine, serine, lysine and arginine. Together with FTIR spectroscopy data, this was consistent with a general model in which the alpha-carboxylate of the amino acid was preferentially bound to the crystal surfaces. Variations in the size and shape of the nanoparticles with amino acid used were consistent with differences in the strength of binding at the HAP surfaces. In comparison, stable colloids could not be prepared with aspartic acid due to a relatively low surface charge; instead, the precipitate consisted of highly elongated nanorods, about 150 x 3.5 nm in dimension. XRD textural analysis suggested a model for nanorod formation based on the oriented aggregation and fusion of primary crystallite domains specifically along the c axis direction. Colloids consisting of HAP/alanine or HAP/arginine nanoparticles were cross-linked in situ by thermal, hydrothermal or chemical polymerisation of surface-attached and unbound amino acids to produce aggregated nanostructures with variable degrees of long-range order. 18 refs.
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Stable suspensions of positively charged nanorods, &lt; 80 nm in length and about 5 nm in width, were obtained in the presence of glycine, alanine, serine, lysine and arginine. Together with FTIR spectroscopy data, this was consistent with a general model in which the alpha-carboxylate of the amino acid was preferentially bound to the crystal surfaces. Variations in the size and shape of the nanoparticles with amino acid used were consistent with differences in the strength of binding at the HAP surfaces. In comparison, stable colloids could not be prepared with aspartic acid due to a relatively low surface charge; instead, the precipitate consisted of highly elongated nanorods, about 150 x 3.5 nm in dimension. XRD textural analysis suggested a model for nanorod formation based on the oriented aggregation and fusion of primary crystallite domains specifically along the c axis direction. 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title SYNTHESIS AND CHARACTERISATION OF AMINO ACID-FUNCTIONALISED HYDROXYAPATITE NANORODS
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