Abstract

Differences in the surface interactions of non-stoichiometric nanocrystalline B-type carbonate-substituted hydroxyapatite (n-cHAp) with the amino acids L-Lysine hydrochloride (L-LysHCl) and L-Arginine hydrochloride (L-ArgHCl) in acidic and alkaline media were determined using structural and spectroscopic analysis methods. The obtained data confirm that hydroxyapatite synthesized using our technique, which was used to develop the n-cHAp/L-LysHCl and n-cHAp/L-ArgHCl composites, is nanocrystalline. Studies of molecular composition of the samples by Fourier transform infrared spectroscopy under the change in the charge state of L-Lysine in environments with different alkalinity are consistent with the results of X-ray diffraction analysis, as evidenced by the redistribution of the modes’ intensities in the spectra that is correlated with the side chains, i.e., amide and carboxyl groups, of the amino acid. During the formation of a biomimetic composite containing L-Lysine hydrochloride and n-cHAp, the interaction occurred through bonding of the L-Lysine side chain and the hydroxyl groups of hydroxyapatite, which created an anionic form of L-Lysine at pH ≤ 5. In contrast, in biocomposites based on L-Arginine and n-cHAp, the interaction only slightly depends on pH value, and it proceeds by molecular orientation mechanisms. The X-ray diffraction and infrared spectroscopy results confirm that changes in the molecular composition of n-cHAp/L-ArgHCl biomimetic composites are caused by the electrostatic interaction between the L-ArgHCl molecule and the carbonate-substituted calcium hydroxyapatite. In this case, the bond formation was detected by Fourier transform infrared (FTIR) spectroscopy; the vibrational modes attributed to the main carbon chain and the guanidine group of L-Arginine are shifted during the interaction. The discovered interaction mechanisms between nanocrystalline carbonate-substituted hydroxyapatite that has physicochemical properties characteristic of the apatite in human dental enamel and specific amino acids are important for selecting the formation conditions of biomimetic composites and their integration with the natural dental tissue.

Highlights

  • Biomimetic composites containing an organic matrix and inorganic phosphate components are promising materials for restorative and regenerative dentistry, surgery and bone grafting [1,2,3]

  • The X-ray diffraction and infrared spectroscopy results confirm that changes in the molecular composition of nanocrystalline B-type carbonatesubstituted hydroxyapatite (n-cHAp)/L-ArgHCl biomimetic composites are caused by the electrostatic interaction between the L-ArgHCl molecule and the carbonate-substituted calcium hydroxyapatite

  • The structural and molecular properties of the amino acids L-LysHCl and L-ArgHCl crystallised from solutions with different pH values were compared with the properties of n-cHAp/L-LysHCl and n-cHAp/L-ArgHCl biomimetic composites obtained under the same conditions and pH values, in order to establish the influence of the charge state of amino acids on the final biocomposite

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Summary

Introduction

Biomimetic composites containing an organic matrix and inorganic phosphate components are promising materials for restorative and regenerative dentistry, surgery and bone grafting [1,2,3]. The synthesis of such hybrid biomaterials, reproducing the physicochemical properties of human hard tissues [4,5,6,7,8], as well as the modification of biomaterials with different inorganic bioactive ions and molecular groups in order to initiate the controlled reaction in tissues and to provide antimicrobic activity, is a complex and multilevel task [9,10,11,12]. Key factors in the formation of a stable bond between the organic (protein) matrix and the phosphate complexes are the presence of amino acid side chains, and the presence of uncompensated charge on the surface of the mineral complexes [20,21,22] and the conditions chosen for the synthesis processes: solvent, temperature, and pH value [23,24]

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