Solid-state NMR and IR characterization of commercial xenogeneic biomaterials used as bone substitutes

Journal of Pharmaceutical and Biomedical Analysis

Volumn 61, Issue , 2012, Pages 136-141

  Kolmas, Joanna ^a   Szwaja, Maciej ^a   Kolodziejski, Waclaw ^a  

^a MEDICAL UNIVERSITY OF WARSAW   (Poland)

Author keywords

Biological apatite; Bone substitute; Infrared spectroscopy; Powder diffraction; Solid state NMR; Xenogeneic biomaterial

Indexed keywords

APATITE; COLLAGEN TYPE 1; HYDROXYAPATITE; NANOCRYSTAL; WATER;

ARTICLE; CHEMICAL COMPOSITION; CONCENTRATION (PARAMETERS); INFRARED SPECTROSCOPY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PARTICLE SIZE; PHYSICAL CHEMISTRY; PRIORITY JOURNAL; SOLID STATE; SOLID STATE NUCLEAR MAGNETIC RESONANCE; THERMOGRAVIMETRY; X RAY DIFFRACTION; XENOGRAFT;

ANIMALS; APATITES; BONE SUBSTITUTES; MAGNETIC RESONANCE SPECTROSCOPY; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; SWINE; TRANSPLANTATION, HETEROLOGOUS; X-RAY DIFFRACTION;

EID: 84856120481     PISSN: 07317085     EISSN: 1873264X     Source Type: Journal    
DOI: 10.1016/j.jpba.2011.11.008     Document Type: Article

References (28)

1. Tudor Ch., Srour S., Thorwarth M., Stockmann P., Neukam F.W., Nkenke E., Schlegel K.A., Felszeghy E. Bone regeneration in osseous defects-application of particulated human and bovine materials. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 2008, 105:430-436.
2. Nannmark U., Sennerby L. The bone tissue responses to prehydrated and collagenated cortico-cancellous porcine bone grafts: a study in rabbit maxillary defects. Clin. Implant Dent. Relat. Res. 2008, 10:264-270.
3. Elliott J.C. Structure and Chemistry of the Apatites and Other Calcium Orthophosphates 1994, Elsevier, Amsterdam.
4. Rey Ch., Combes C., Drouet C., Sfihi H. Chemical Diversity of Apatites. Adv. Sci. Technol. 2006, 49:27-36.
5. Figueiredo M., Henriques J., Martins G., Guerra F., Judas F., Figueiredo H. Physicochemical characterization of biomaterials commonly used in dentistry as bone substitutes-comparison with human bone. J. Biomed. Mater. Res. B 2010, 92:409-419.
6. Tadic D., Epple M. A thorough physiochemical characterization of 14 calcium phosphate-based bone substitution materials in comparison to natural bone. Biomaterials 2004, 25:987-994.
7. da Cruz G.A., de Toledo S., Sallum E.A., de Lima A.F.M. Morphological and chemical analysis of bone substitutes by scanning electron microscopy and microanalysis by spectroscopy of dispersion energy. Braz. Dent. J. 2007, 18:129-133.
8. Accorsi-Mendonça T., Conz M.B., Barros T.C., de Sena L.A., de Almeida Soares G., Granjeiro J.M. Physicochemical characterization of two deproteinized bovine xenografts. Braz. Oral Res. 2008, 22:5-10.
9. Ślósarczyk A., Paszkiewicz Z., Paluszkiewicz Cz. FTIR and XRD evaluation of carbonated hydroxyapatite powders synthesized by wet methods. J. Mol. Struct. 2005, 744-747:657-661.
10. 1H cross-polarization. Chem. Commun. 2007, 4390-4392.
11. 31P MAS NMR. Solid State NMR 2007, 32:53-58.
12. Dorozhkin S.V. Nanosized and nanocrystalline calcium orthophosphates. Acta Biomater. 2010, 6:715-734.
13. Huster D. Solid-state NMR studies of collagen structure and dynamics in isolated fibrils and in biological tissues. Ann. Rep. NMR Spectrosc. 2008, 64:127-159.
14. Beshah K., Rey C., Glimcher M.J., Shimizu M., Griffin R.G. Solid state carbon-13 and proton NMR studies of carbonate-containing calcium phosphates and enamel. J. Solid State Chem. 1990, 85:71-81.
15. 31P CP MAS NMR. Langmuir 2006, 22:4787-4792.
16. Wu Y., Glimcher M.J., Rey C., Ackerman J.L. A unique protonated phosphate group in bone mineral not present in synthetic phosphates: identification by phosphorus-31 solid state NMR spectroscopy. J. Mol. Biol. 1994, 244:423-435.
17. Kolodziejski W. Solid-state NMR of bone. Top. Curr. Chem. 2005, 246:235-270.
18. Cho G., Wu Y., Ackerman J.L. Detection of hydroxyl ions in bone mineral by solid-state NMR spectroscopy. Science 2003, 300:1123-1127.
19. Kaflak A., Ślosarczyk A., Kolodziejski W. A comparative study of carbonate bands from nanocrystalline carbonated hydroxyapatites using FT-IR spectroscopy in the transmission and photoacoustic modes. J. Mol. Struct. 2011, 997:7-14.
20. Kaflak A., Kolodziejski W. Complementary information of water and hydroxyl groups in nanocrystalline carbonated hydroxyapatites from TGA, NMR and IR measurements. J. Mol. Struct. 2011, 990:263-270.
21. Rey Ch., Collins B., Goehl T., Dickson I.R., Glimcher M.J. The carbonate environment in bone mineral, a resolution-enhanced Fourier transform infrared spectroscopy study. Calcif. Tissue Int. 1989, 45:157-164.
22. Fleet M.E., Xiaoyang Y., King P.L. Accommodation of the carbonate ion in apatite: an FTIR and X-ray structure study of crystals synthesized at 2-4GPa. Am. Mineral. 2004, 89:1422-1432.
23. Clasen A.B.S., Ruyter I.E. Quantitative determination of type A and type B carbonate in human deciduous and permanent enamel by means of Fourier transform infrared spectrometry. Adv. Dent. Res. 1997, 11:523-527.
24. Belbachir K., Noreen R., Gouspillou G., Petibois C. Collagen types analysis and differentiation by FTIR spectroscopy. Anal. Bioanal. Chem. 2009, 395:829-837.
25. Magne D., Weiss P., Bouler J.-M., Laboux O., Daclusi G. Study of the maturation of the organic (type I collagen) and mineral (nonstoichiometric apatite) constituents of a calcified tissue (dentin) as a function of location: a Fourier transform infrared microspectroscopic investigation. J. Bone Miner. Res. 2001, 16:750-756.
26. Eichert D., Drouet C., Sfihi H., Rey C., Combes C. Nanocrystalline Apatite-based Biomaterials 2009, Nova Science Publishers, Inc., New York.
27. 3- vibration. Biochim. Biophys. Acta 2001, 1527:11-19.
28. 4 domain. Calcif. Tissue Int. 1990, 46:384-394.