Cerium doping of 45S5 bioactive glass improves redox potential and cellular bioactivity
- Jeong-Hyun Ryu 1, Tae-Yun Kang 2, Sung-Hwan Choi 1, Jae-Sung Kwon 3,4, Min-Ho Hong 5
- Jeong-Hyun Ryu 1, Tae-Yun Kang 2, Sung-Hwan Choi 1
- 1Department of Orthodontics, Institute of Craniofacial Deformity, Yonsei University College of Dentistry, Seoul, 03722, Republic of Korea.
- 2Department and Research Institute for Dental Biomaterials and Bioengineering, Yonsei University College of Dentistry, Seoul, 03722, Republic of Korea.
- 3Department and Research Institute for Dental Biomaterials and Bioengineering, Yonsei University College of Dentistry, Seoul, 03722, Republic of Korea. jkwon@yuhs.ac.
- 4BK21 FOUR Project, Yonsei University College of Dentistry, Seoul, 03722, Republic of Korea. jkwon@yuhs.ac.
- 5Department of Dental Biomaterials and Research Institute of Oral Science, College of Dentistry, Gangneung-Wonju National University, Gangneung, 25457, Republic of Korea. mhong@gwnu.ac.kr.
- 0Department of Orthodontics, Institute of Craniofacial Deformity, Yonsei University College of Dentistry, Seoul, 03722, Republic of Korea.
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View abstract on PubMed
Summary
This summary is machine-generated.This study synthesized cerium dioxide-doped bioglass (CBG) materials for hard tissue repair. CBG enhanced cellular activity and bone mineralization, showing potential for therapeutic applications.
Area Of Science
- Biomaterials Science
- Materials Chemistry
- Biomedical Engineering
Background
- 45S5 Bioglass (BG) is a silicate-based glass used in hard tissue therapy.
- Nanoceria (CeO2) exhibits redox properties and enhances biological responses.
- The optimal proportion of CeO2 doping in BG for cellular bioactivity is not well-established.
Purpose Of The Study
- To synthesize and characterize a series of cerium dioxide-doped bioglass (CBG) materials.
- To investigate the effect of varying CeO2 doping concentrations (1-12 wt.%) on the properties and bioactivity of BG.
- To evaluate the potential of CBG for hard tissue therapeutic applications.
Main Methods
- Synthesis of CBG series with increasing CeO2 content.
- Characterization of glass structure, redox states of Ce, and antioxidant activity.
- Assessment of mineralization capacity and cellular activity (proliferation, alkaline phosphatase activity, osteogenic gene expression) of CBG compared to BG.
- Evaluation of biomineralization enhancement.
Main Results
- CBG series maintained a stable glass network structure, similar to BG.
- CBG exhibited antioxidant activity due to the Ce3+/Ce4+ redox states.
- CBG promoted pre-osteoblastic cell proliferation, alkaline phosphatase activity, and osteogenic gene expression.
- CBG enhanced biomineralization compared to BG.
Conclusions
- The synthesized CBG series demonstrates preserved bioactivity and enhanced osteogenic properties.
- The CeO2 doping effectively improved cellular responses and biomineralization.
- CBG shows significant potential for applications in hard tissue regeneration and therapy.
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