Multifunctional Lithium-Doped Mesoporous Nanoparticles for Effective Dentin Regeneration in vivo

被引:4
作者
Liang, Zitian [1 ]
Chen, Ding [2 ]
Jiang, Ye [1 ]
Su, Zhikang [2 ]
Pi, Yixing [2 ]
Luo, Tao [2 ]
Jiang, Qianzhou [1 ]
Yang, Li [1 ,3 ]
Guo, Lvhua [2 ,3 ]
机构
[1] Guangzhou Med Univ, Affiliated Stomatol Hosp, Guangdong Engn Res Ctr Oral Restorat & Reconstruct, Dept Endodont,Guangzhou Key Lab Basic & Appl Res O, Guangzhou 510182, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Guangdong Engn Res Ctr Oral Restorat & Reconstruct, Dept Prosthodont, Affiliated Stomatol Hosp,Guangzhou Key Lab Basic &, Guangzhou 510182, Guangdong, Peoples R China
[3] Guangzhou Med Univ, Affiliated Stomatol Hosp, 195 West Dongfeng Rd, Guangzhou 510182, Peoples R China
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2023年 / 18卷
关键词
lithium; mesoporous nanoparticles; dental pulp stem cells; dentin regeneration; Wnt/I3-catenin signaling pathway; antibacterial properties; MINERAL TRIOXIDE AGGREGATE; OSTEOGENIC DIFFERENTIATION; ANTIBACTERIAL ACTIVITY; BIOACTIVE GLASSES; CELLS; VITRO; TOOTH; ACTIVATION; RELEASE; PATHWAY;
D O I
10.2147/IJN.S424930
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Introduction: Effective infection control without irritating the pulp tissue is the key to successful vital pulp therapy. Developing a novel antibacterial biomaterial that promotes dentin regeneration for pulp capping is thus a promising strategy for enhancing vital pulp therapy.Methods: Lithium-doped mesoporous nanoparticles (Li-MNPs) were synthesized using an alkali-catalyzed sol-gel method. The particle size, elemental distribution, surface morphology, pore structure, and ion release from Li-MNPs were measured. Human dental pulp stem cells (hDPSCs) and Streptococcus mutans (S. mutans) were used to evaluate the biological effects of Li-MNPs. In addition, a dental pulp exposure mouse model was used to evaluate the regenerative effects of Li-MNPs.Results: Li-MNPs had a larger surface area (221.18 m2/g), a larger pore volume (0.25 cm3/g), and a smaller particle size (520.92 & PLUSMN; 35.21 nm) than MNPs. The in vitro investigation demonstrated that Li-MNPs greatly enhanced the biomineralization and odontogenic differentiation of hDPSCs through the Wnt/I3-catenin signaling pathway. Li-MNPs showed a strong antibacterial effect on S. mutans. As expected, Li-MNPs significantly promoted dentin regeneration in situ and in vivo.Conclusion: Li-MNPs promoted dentin regeneration and inhibited S. mutans growth, implying a possible application as a pulp capping agent in vital pulp therapy.
引用
收藏
页码:5309 / 5325
页数:17
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