Five different concentrations of lanthanum (La(3+)) substituted β-tricalcium phosphate [β-TCP, β-Ca3(PO4)2] were formed through aqueous precipitation technique and the results were compared with stoichiometric β-TCP. All the La(3+) substituted β-TCP powders were characterized using XRD, FT-IR, XRF, Raman spectroscopy and Rietveld refinement of the XRD data. The results from the investigation confirmed the presence of La(3+) in rhombohedral β-TCP structure. The substitution of higher sized of La(3+) led to the considerable enhancement in lattice parameters of β-TCP crystal structure and La(3+) was found to have occupied the eight fold coordinated Ca (3) site of β-TCP structure. La(3+) occupancy at the Ca (3) site resulted in the significant distortions of the associated PO4 tetrahedra, which were supported by the Raman and FT-IR spectroscopic techniques. La(3+) presence in the crystal lattice of β-TCP also led to the delay in allotropic phase transformation of β-TCP to α-TCP till 1300°C, thus signifying the good thermal stability of La(3+) substituted β-TCP powders. The antibacterial efficiency of La(3+) substituted β-TCP powders was confirmed from the in vitro tests done on microbes such as Staphylococcus aureus and Escheria coli. Further, the presence of La(3+) in the crystal lattice of β-TCP did not affect the hardness and Young's modulus values of β-TCP.
Keywords: Antibacterial; Lanthanum; Mechanical; Thermal stability; β-Ca(3)(PO(4))(2).
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