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1.
Biomed Mater Eng ; 28(6): 621-631, 2017.
Article in English | MEDLINE | ID: mdl-29171967

ABSTRACT

BACKGROUND: Reconstruction of bone defects is often performed using bone autografts. However, limitations associated with the use of autografts led to the use of bone substitute materials. OBJECTIVES: The purpose of this study was to compare the surface characteristics of three commercially available grafts namely allografts, xenografts and alloplasts. METHODS: This in vitro study was conducted on beta-tricalcium phosphate (ß-TCP) alloplast, a mixture of demineralized bone matrix and mineralized bone allograft (DBM&MBA) and natural bovine bone mineral (NBBM) xenograft. Presence of apatite groups on the surface of samples was assessed by X-ray diffraction (XRD) while the presence of functional groups was evaluated using Fourier transform infrared spectroscopy (FTIR). Also, dental pulp stem cells (DPSCs) were cultured on the surface of samples and their adhesion was evaluated under a scanning electron microscope (SEM). RESULTS: The FTIR showed a relatively similar pattern for NBBM and TCP samples and a different pattern in DBM&MBA. The results of XRD analysis also showed similarities between NBBM and TCP with sharper peaks than the DBM&MBA sample. The SEM micrographs showed that at 24 hours, no cell was detectable on the surface of NBBM sample; whereas, elongated cells were noted on the surface of TCP and DBM&MBA samples. CONCLUSIONS: The patterns of ß-TCP and NBBM samples in XRD and FTIR spectroscopy showed high resemblance but they had different behaviors with respect to cell adhesion.


Subject(s)
Bone Matrix/chemistry , Bone Substitutes/chemistry , Bone Transplantation , Calcium Phosphates/chemistry , Stem Cells/cytology , Tissue Scaffolds/chemistry , Animals , Cattle , Cell Adhesion , Cell Proliferation , Cells, Cultured , Humans , Surface Properties
2.
J Mater Sci Mater Med ; 27(11): 164, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27655430

ABSTRACT

Bone autografts are often used for reconstruction of bone defects; however, due to the limitations of autografts, researchers have been in search of bone substitutes. Dentin is of particular interest for this purpose due to high similarity to bone. This in vitro study sought to assess the surface characteristics and biological properties of dentin samples prepared with different treatments. This study was conducted on regular (RD), demineralized (DemD), and deproteinized (DepD) dentin samples. X-ray diffraction and Fourier transform infrared spectroscopy were used for surface characterization. Samples were immersed in simulated body fluid, and their bioactivity was evaluated under a scanning electron microscope. The methyl thiazol tetrazolium assay, scanning electron microscope analysis and quantitative real-time polymerase chain reaction were performed, respectively to assess viability/proliferation, adhesion/morphology and osteoblast differentiation of cultured human dental pulp stem cells on dentin powders. Of the three dentin samples, DepD showed the highest and RD showed the lowest rate of formation and deposition of hydroxyapatite crystals. Although, the difference in superficial apatite was not significant among samples, functional groups on the surface, however, were more distinct on DepD. At four weeks, hydroxyapatite deposits were noted as needle-shaped accumulations on DemD sample and numerous hexagonal HA deposit masses were seen, covering the surface of DepD. The methyl thiazol tetrazolium, scanning electron microscope, and quantitative real-time polymerase chain reaction analyses during the 10-day cell culture on dentin powders showed the highest cell adhesion and viability and rapid differentiation in DepD. Based on the parameters evaluated in this in vitro study, DepD showed high rate of formation/deposition of hydroxyapatite crystals and adhesion/viability/osteogenic differentiation of human dental pulp stem cells, which may support its osteoinductive/osteoconductive potential for bone regeneration.


Subject(s)
Dentin/chemistry , Apatites/chemistry , Body Fluids , Bone Regeneration , Bone Transplantation , Cell Adhesion , Cell Proliferation , Cell Survival , Dental Pulp/cytology , Durapatite/chemistry , Gene Expression Regulation , Humans , Microscopy, Electron, Scanning , Osteoblasts/metabolism , Osteogenesis , Powders , Real-Time Polymerase Chain Reaction , Spectroscopy, Fourier Transform Infrared , Stem Cells/cytology , Tissue Scaffolds , X-Ray Diffraction
3.
J Biomed Mater Res A ; 104(10): 2616-27, 2016 10.
Article in English | MEDLINE | ID: mdl-27256548

ABSTRACT

Dentin has become an interesting potential biomaterial for tissue engineering of oral hard tissues. It can be used as a scaffold or as a source of growth factors in bone tissue engineering. Different forms of dentin have been studied for their potential use as bone substitutes. Here, we systematically review different methods of dentin preparation and the efficacy of processed dentin in bone tissue engineering. An electronic search was carried out in PubMed and Scopus databases for articles published from 2000 to 2016. Studies on dentin preparation for application in bone tissue engineering were selected. The initial search yielded a total of 1045 articles, of which 37 were finally selected. Review of studies showed that demineralization was the most commonly used dentin preparation process for use in tissue engineering. Dentin extract, dentin particles (tooth ash), freeze-dried dentin, and denatured dentin are others method of dentin preparation. Based on our literature review, we can conclude that preparation procedure and the size and shape of dentin particles play an important role in its osteoinductive and osteoconductive properties. Standardization of these methods is important to draw a conclusion in this regard. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 2616-2627, 2016.


Subject(s)
Bone Substitutes/chemistry , Bone Substitutes/pharmacology , Dentin/chemistry , Osteogenesis/drug effects , Tissue Engineering/methods , Tissue Scaffolds/chemistry , Animals , Humans
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