The effects of biphasic calcium phosphate and simvastatin on human dental pulp cells in vitro on dentin regeneration

This study was conducted to prepare an appropriate biphasic calcium phosphate (BCP) scaffold in combination with optimal concentration of simvastatin to induce human dental pulp cells differentiation and dentin tissue regeneration. BCP scaffold of 20/80 hydroxyapatite (HA) to β-tricalcium phospha...

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Main Author: Abdul Qader Al-Kukasih, Sarah Talib
Format: Thesis
Language:English
Published: 2015
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Online Access:http://eprints.usm.my/40802/1/Dr._Sarah_Talib_Abdul_Qader-24_pages.pdf
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spelling my-usm-ep.408022019-02-10T07:50:14Z The effects of biphasic calcium phosphate and simvastatin on human dental pulp cells in vitro on dentin regeneration 2015-12 Abdul Qader Al-Kukasih, Sarah Talib RK Dentistry This study was conducted to prepare an appropriate biphasic calcium phosphate (BCP) scaffold in combination with optimal concentration of simvastatin to induce human dental pulp cells differentiation and dentin tissue regeneration. BCP scaffold of 20/80 hydroxyapatite (HA) to β-tricalcium phosphate (β-TCP) ratio with micropores < 10 μm, macropores of 300 μm, and porosity of 65 % was successfully synthesized using wet precipitation method and polyethylene microspheres as pore-creating agents. The scaffold was characterized using x-ray diffraction (XRD), fourier transform infra-red spectroscopy (FTIR), x-ray fluorescence (XRF), field emission scanning electron microscope (FESEM), linear shrinkage, and total porosity measurements. BCP sample extract was prepared and combined with four different concentrations of simvastatin (2.0, 1.5, 1.0 and 0.5 μM) for the assessment of cell viability using MTT (3-(4,5- dimethyl-thiazoyl)-2,5-diphenyl-tetrazolium bromide) assay. The alkaline phosphatase activity was assessed using alkaline phosphatase assay. The groups which showed the best cell viability and alkaline phosphatase activity were selected. They were assessed for both odontogenic differentiation potential of collagen type I alpha 1 (COL1A1), bone sialoprotein (BSP), dentin matrix protein-1 (DMP-1), dentin sialophosphoprotein (DSPP), and Runt-related transcription factor-2 (RUNX-2) genes expression analysis using reverse transcription-polymerase chain reaction (RT-PCR) and extracellular matrix mineralization detection using Alizarin Red S staining. The results showed that combination groups of BCP +1.5 μM, BCP + 1.0 μM, and BCP + 0.5 μM had higher mean cell viability index, except BCP + 2.0 μM that showed cytotoxicity. For alkaline phosphatase activity, the combination groups of BCP + 1.5 μM, BCP +1.0 μM, and BCP + 0.5 μM showed higher mean alkaline phosphatase activity index with BCP + 1.5 μM the highest. For the odontogenic differentiation potential, BCP + 1.5 μM combination group showed up-regulation of COL1A1, DMP-1, BSP, and DSPP genes and down-regulation of RUNX-2 gene. For the extracellular matrix mineralization, BCP + 1.5 μM combination group showed the highest ability to induce the mineral deposition. In conclusion, the combination of BCP and 1.5 μM simvastatin achieved together a preferable induction of human dental pulp cells differentiation toward dentin tissue regeneration. 2015-12 Thesis http://eprints.usm.my/40802/ http://eprints.usm.my/40802/1/Dr._Sarah_Talib_Abdul_Qader-24_pages.pdf application/pdf en public masters Universiti Sains Malaysia Pusat Pengajian Sains Perubatan
institution Universiti Sains Malaysia
collection USM Institutional Repository
language English
topic RK Dentistry
spellingShingle RK Dentistry
Abdul Qader Al-Kukasih, Sarah Talib
The effects of biphasic calcium phosphate and simvastatin on human dental pulp cells in vitro on dentin regeneration
description This study was conducted to prepare an appropriate biphasic calcium phosphate (BCP) scaffold in combination with optimal concentration of simvastatin to induce human dental pulp cells differentiation and dentin tissue regeneration. BCP scaffold of 20/80 hydroxyapatite (HA) to β-tricalcium phosphate (β-TCP) ratio with micropores < 10 μm, macropores of 300 μm, and porosity of 65 % was successfully synthesized using wet precipitation method and polyethylene microspheres as pore-creating agents. The scaffold was characterized using x-ray diffraction (XRD), fourier transform infra-red spectroscopy (FTIR), x-ray fluorescence (XRF), field emission scanning electron microscope (FESEM), linear shrinkage, and total porosity measurements. BCP sample extract was prepared and combined with four different concentrations of simvastatin (2.0, 1.5, 1.0 and 0.5 μM) for the assessment of cell viability using MTT (3-(4,5- dimethyl-thiazoyl)-2,5-diphenyl-tetrazolium bromide) assay. The alkaline phosphatase activity was assessed using alkaline phosphatase assay. The groups which showed the best cell viability and alkaline phosphatase activity were selected. They were assessed for both odontogenic differentiation potential of collagen type I alpha 1 (COL1A1), bone sialoprotein (BSP), dentin matrix protein-1 (DMP-1), dentin sialophosphoprotein (DSPP), and Runt-related transcription factor-2 (RUNX-2) genes expression analysis using reverse transcription-polymerase chain reaction (RT-PCR) and extracellular matrix mineralization detection using Alizarin Red S staining. The results showed that combination groups of BCP +1.5 μM, BCP + 1.0 μM, and BCP + 0.5 μM had higher mean cell viability index, except BCP + 2.0 μM that showed cytotoxicity. For alkaline phosphatase activity, the combination groups of BCP + 1.5 μM, BCP +1.0 μM, and BCP + 0.5 μM showed higher mean alkaline phosphatase activity index with BCP + 1.5 μM the highest. For the odontogenic differentiation potential, BCP + 1.5 μM combination group showed up-regulation of COL1A1, DMP-1, BSP, and DSPP genes and down-regulation of RUNX-2 gene. For the extracellular matrix mineralization, BCP + 1.5 μM combination group showed the highest ability to induce the mineral deposition. In conclusion, the combination of BCP and 1.5 μM simvastatin achieved together a preferable induction of human dental pulp cells differentiation toward dentin tissue regeneration.
format Thesis
qualification_level Master's degree
author Abdul Qader Al-Kukasih, Sarah Talib
author_facet Abdul Qader Al-Kukasih, Sarah Talib
author_sort Abdul Qader Al-Kukasih, Sarah Talib
title The effects of biphasic calcium phosphate and simvastatin on human dental pulp cells in vitro on dentin regeneration
title_short The effects of biphasic calcium phosphate and simvastatin on human dental pulp cells in vitro on dentin regeneration
title_full The effects of biphasic calcium phosphate and simvastatin on human dental pulp cells in vitro on dentin regeneration
title_fullStr The effects of biphasic calcium phosphate and simvastatin on human dental pulp cells in vitro on dentin regeneration
title_full_unstemmed The effects of biphasic calcium phosphate and simvastatin on human dental pulp cells in vitro on dentin regeneration
title_sort effects of biphasic calcium phosphate and simvastatin on human dental pulp cells in vitro on dentin regeneration
granting_institution Universiti Sains Malaysia
granting_department Pusat Pengajian Sains Perubatan
publishDate 2015
url http://eprints.usm.my/40802/1/Dr._Sarah_Talib_Abdul_Qader-24_pages.pdf
_version_ 1747820825568870400