The impact of hydroxyapatite on alkaline phosphatase activity and mineral deposition of dental pulp stem cells using a double antibiotic paste loaded methylcellulose carrier

dc.contributor.advisorBruzzaniti, Angela
dc.contributor.authorFischer, Benjamin I.
dc.contributor.otherSpolnik, Kenneth
dc.contributor.otherEhrlich, Ygal
dc.contributor.otherBringas, Josef
dc.contributor.otherGregory, Richard
dc.date.accessioned2020-06-27T11:00:30Z
dc.date.available2020-06-27T11:00:30Z
dc.date.issued2020
dc.degree.date2020en_US
dc.degree.disciplineSchool of Dentistryen
dc.degree.grantorIndiana Universityen_US
dc.degree.levelM.S.D.en_US
dc.descriptionIndiana University-Purdue University Indianapolis (IUPUI)en_US
dc.description.abstractIntroduction: Regenerative endodontic procedures (REPs) are a type of endodontic treatment aimed at replacing damaged tooth structures, including dentin and root structures, as well as cells of the pulp-dentin complex. Double antibiotic paste (DAP) has been shown to be efficacious in achieving disinfection of the root canal system while minimizing cytotoxicity to dental pulp stem cells (DPSCs). Hydroxyapatite (HA) is an extracellular, mineralized component of bone that has shown much promise as a scaffold in the field of regenerative medicine. Objective: The objective of this study was to evaluate the effects of HA in a DAP loaded methylcellulose (MC) carrier on the differentiation and mineral deposition of DPSC over time. Materials and Methods: DPSCs were plated in 24-well plates with culture media. The following day, semi-permeable 0.1 m chambers were inserted into the wells to separate the reservoirs and permit delivery of medicaments. 100 L treatment paste composed of MC with 1% DAP and either 0.5% or 1.0% nano-HA was added, followed by additional culture media. After 3 days of treatment, medicaments were removed and DPSCs were cultured for an additional 9 days with replacement of media every 3-4 days. At Day 12, DPSCs were evaluated for alkaline phosphatase (ALP) activity using a biochemical assay and mineral deposition using an Alizarin Red S Ca2+ staining assay (4 wells/group). Comparisons between groups were performed using one-way analysis of variance (ANOVA) with a 5% significance level used for all tests. Results: A trend towards increased ALP and mineral deposition activity was noted among the groups with HA added to DAP with MC. Although these trends were not statistically significant, a trend towards increased ALP and mineral deposition was observed after 3-day medicament exposure. The results were similar to previous findings using 7-day medicament treatments. Conclusion: The addition of HA showed a trend towards improved differentiation and mineral deposition of DPSCs compared to DAP with MC. Although additional studies are required, these results showed suggest that even with a shortened treatment time, increased differentiation and mineral deposition of DPSCs may be possible. This study provides additional support that low concentration DAP in a MC carrier has potential application in regenerative endodontic procedures. The novel addition of HA may provide additional osteogenic potential.en_US
dc.identifier.urihttps://hdl.handle.net/1805/23133
dc.identifier.urihttp://dx.doi.org/10.7912/C2/1656
dc.language.isoen_USen_US
dc.subjectdouble antibiotic pasteen_US
dc.subjecthydroxyapatiteen_US
dc.subjectmethylcelluloseen_US
dc.subjectstem cellsen_US
dc.subjectmineral depositionen_US
dc.subjectdifferentiationen_US
dc.subject.meshAlkaline Phosphatase
dc.subject.meshAnti-Bacterial Agents
dc.subject.meshCell Differentiation
dc.subject.meshDental Pulp
dc.subject.meshHydroxyapatites
dc.subject.meshMethylcellulose
dc.subject.meshRegenerative Endodontics
dc.subject.meshStem Cells
dc.titleThe impact of hydroxyapatite on alkaline phosphatase activity and mineral deposition of dental pulp stem cells using a double antibiotic paste loaded methylcellulose carrieren_US
dc.typeThesisen
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