Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2022Modified Taq DNA Polymerase for Allele-Specific Ultra-Sensitive Detection of Genetic Variants.9citations
  • 2019Ceria-incorporated MTA for accelerating odontoblastic differentiation via ROS downregulation.30citations

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Chart of shared publication
Ih, Park
1 / 1 shared
Baek, K.
1 / 1 shared
Lim, Youngshin
1 / 1 shared
Bc, Lee
1 / 1 shared
Cho, G.
1 / 2 shared
Hw, Kim
1 / 3 shared
Hr, Kim
1 / 4 shared
Jh, Lee
1 / 2 shared
Jh, Park
1 / 1 shared
Jy, Yoon
1 / 1 shared
Sk, Jun
1 / 1 shared
Chart of publication period
2022
2019

Co-Authors (by relevance)

  • Ih, Park
  • Baek, K.
  • Lim, Youngshin
  • Bc, Lee
  • Cho, G.
  • Hw, Kim
  • Hr, Kim
  • Jh, Lee
  • Jh, Park
  • Jy, Yoon
  • Sk, Jun
OrganizationsLocationPeople

article

Ceria-incorporated MTA for accelerating odontoblastic differentiation via ROS downregulation.

  • Hw, Kim
  • Hr, Kim
  • Hh, Lee
  • Jh, Lee
  • Jh, Park
  • Jy, Yoon
  • Sk, Jun
Abstract

<h4>Objective</h4>Odontoblast differentiation from dental pulp stem cells (DPSCs) is involved in a cascade of key biological events for maintaining pulp-dentin homeostasis, repair and regeneration. A pulp regeneration biomaterial (mineral trioxide aggregate (MTA)) increased intracellular reactive oxygen species (ROS) levels during differentiation, ameliorating the differentiating of DPSCs into odontoblasts. Here, ceria nanoparticles (CNP) were incorporated as an insoluble antioxidant into commercially available MTA (CMTA), and the odontoblastic differentiation of human DPSCs was investigated.<h4>Methods</h4>The CMTA was fabricated from MTA and CNP conjugation up to 4wt%, and the compressive strength, surface morphology after setting and setting time were investigated. Furthermore, the alkaline phosphatase (ALP) assay, Alizarin Red staining (ARS) and quantitative real-time polymerase chain reaction (qPCR) were performed to evaluate odontoblastic differentiation in an indirect co-culture system using inserts with pores. To reveal the underlying mechanism, the ROS levels and ion release were measured. Statistical analysis was performed by one-way analysis of variance with a Tukey post hoc test (P<0.05).<h4>Results</h4>CMTA significantly elevated the odontoblastic differentiation of hDPSCs measured by ALP activity, ARS, and odontoblastic gene expression, whereas the other physico-mechanical properties were relatively maintained. Upregulation of gene expression from CMTA was reversed with hydrogen peroxide. CMTA could reduce the increased intracellular ROS levels of hDPSCs by approximately 70% during differentiation, similar to when an antioxidant was used, without changing the ion release and pH of the media.<h4>Significance</h4>CMTA could be useful dental materials for regenerating dentin-pulp complexes by instructing intracellular ROS during differentiation to achieve beneficial biological functions. This study suggests a new direction of dental nanomaterials in treating pulp-dentin complexes.

Topics
  • nanoparticle
  • impedance spectroscopy
  • pore
  • mineral
  • surface
  • Oxygen
  • reactive
  • strength
  • Hydrogen