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      Are different crystallinity-index-calculating methods of hydroxyapatite efficient and consistent?

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          Abstract

          Different CI-calculating methods of XRD, FTIR and Raman techniques showed high efficiency and consistency.

          Abstract

          Crystallinity is related to the degree of order and the crystal size of a given crystalline substance. It can affect the quality of hydroxyapatite (HA) and its abnormality can lead to diseases of hard mineralized tissues. Crystallinity index (CI) is a quantitative indicator of crystallinity. Various techniques, such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy, and many methods based on these techniques have been used to define the CI of HA. The present study compares these methods and summarizes their characters for hydrothermally synthesized HA crystals with different aging time. Additionally, correlation coefficients between CIs calculated by different methods and crystal size ( R 1 2) and correlation coefficients among various CIs ( R 2 2) were obtained from linear-regression analysis. Scanning electron microscopy (SEM) was utilized as a supplementary technique to observe the morphological changes during the HA aging process. The results showed larger crystal size, increased crystallinity and more regular morphology of HA with increased aging time. All the R 1 2 and R 2 2 were above 0.9 and there were no significant differences between R 1 2. However, different CI-calculating methods showed individual characters or limitations during their application. Such results suggested XRD, FTIR and Raman techniques used in this study were generally consistent and efficient but their special characters should be considered during their application. Researchers should choose certain appropriate technique and method to obtain CI on the basis of sample characteristics and experimental conditions.

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          Most cited references40

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          CRYSTAL STRUCTURE OF HYDROXYAPATITE.

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            Micro-Raman and FTIR studies of synthetic and natural apatites.

            B-type synthetic carbonate hydroxyapatite (CHAp), natural carbonate fluorapatite (CFAp) and silicon-substituted hydroxyapatite (SiHAp) have been studied by using micro-Raman and infrared (IR) spectroscopy. It was found that while B-type carbonate substitution predominates in carbonate apatites (CAps), A-type is also detected. B-type carbonate substitution causes a broadening of the v(1) P-O stretching mode that is associated with the atomic disorder and lowering of the local symmetry in CAps from C(6h)(2) to C(3h). An approximately 15 cm(-1) shift of the v(3c) PO(4) stretching IR mode was observed upon decarbonation of the CFAp. Such shift which was confirmed by lattice dynamics calculations points out that the P-O bond lengths on the mirror plane increase when carbonate leaves the apatite structure. The present results support the substitution mechanism proposed on the basis of neutron powder diffraction studies of the same samples whereby carbonate substitutes on the mirror plane of the phosphate tetrahedron. The intensity ratios of the v(2) IR CO(3) and v(1) PO(4) bands in samples of various carbonate contents provide a measure of the degree of carbonation for CAps.
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              Application of vibrational spectroscopy to the study of mineralized tissues (review).

              The infrared and Raman spectroscopy of bone and teeth tissues are reviewed. Characteristic spectra are obtained for both the mineral and protein components of these tissues. Vibrational spectroscopy is used to study the mineralization process, to define the chemical structure changes accompanying bone diseases, and to characterize interactions between prosthetic implants and tissues. Microspectroscopy allows acquisition of spatially resolved spectra, with micron scale resolution. Recently developed imaging modalities allow tissue imaging with chemical composition contrast.
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                Author and article information

                Contributors
                Journal
                NJCHE5
                New Journal of Chemistry
                New J. Chem.
                Royal Society of Chemistry (RSC)
                1144-0546
                1369-9261
                2017
                2017
                : 41
                : 13
                : 5723-5731
                Affiliations
                [1 ]The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education
                [2 ]School & Hospital of Stomatology
                [3 ]Wuhan University
                [4 ]Wuhan 430079
                [5 ]P. R. China
                [6 ]Department of Oral Biology
                [7 ]School of Dental Medicine
                [8 ]University of Pittsburgh
                [9 ]Pittsburgh
                [10 ]USA
                Article
                10.1039/C7NJ00803A
                7a9737ac-967a-4436-b88f-26a8ef91cfb9
                © 2017
                History

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