A deformable SIS/HA composite hydrogel coaxial scaffold promotes alveolar bone regeneration after tooth extraction

被引:2
|
作者
Ma, Shiqing [1 ]
Li, Yumeng [2 ]
Yao, Shiyu [2 ]
Shang, Yucheng [2 ]
Li, Rui [2 ]
Ling, Lijuan [3 ]
Fu, Wei [1 ]
Wei, Pengfei [4 ]
Zhao, Bo [4 ]
Zhang, Xuesong [5 ]
Deng, Jiayin [2 ]
机构
[1] Tianjin Med Univ, Hosp 2, Dept Stomatol, Tianjin 300211, Peoples R China
[2] Tianjin Med Univ, Sch & Hosp Stomatol, Tianjin 300070, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, JingZhong MED Huangsi Out Patient Dept, Beijing 100120, Peoples R China
[4] Beijing Biosis Healing Biol Technol Co Ltd, Beijing 102600, Peoples R China
[5] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 4, Dept Orthopaed, Beijing 100048, Peoples R China
关键词
SIS/HA; Exosome; Antibacterial; Osteogenesis; Angiogenesis; Alveolar ridge preservation; RIDGE PRESERVATION; TISSUE; HYDROXYAPATITE; ANTIBACTERIAL; CARTILAGE; EXOSOMES; IMPROVES;
D O I
10.1016/j.bioactmat.2024.12.008
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
After tooth extraction, alveolar bone absorbs unevenly, leading to soft tissue collapse, which hinders full regeneration. Bone loss makes it harder to do dental implants and repairs. Inspired by the biological architecture of bone, a deformable SIS/HA (Small intestinal submucosa/Hydroxyapatite) composite hydrogel coaxial scaffold was designed to maintain bone volume in the socket. The SIS/HA scaffold containing GL13K as the outer layer, mimicking compact bone, while SIS hydrogel loaded with bone marrow mesenchymal stem cells-derived exosomes (BMSCs-Exos) was utilized as the inner core of the scaffolds, which are like soft tissue in the skeleton. This coaxial scaffold exhibited a modulus of elasticity of 0.82 MPa, enabling it to adaptively fill extraction sockets and maintain an osteogenic space. Concurrently, the inner layer of this composite scaffold, enriched with BMSCsExos, promoted the proliferation and migration of human umbilical vein endothelial cells (HUVECs) and BMSCs into the scaffold interior (approximate to 3-fold to the control), up-regulated the expression of genes related to osteogenesis (BMP2, ALP, RUNX2, and OPN) and angiogenesis (HIF-1 alpha and VEGF). This induced new blood vessels and bone growth within the scaffold, addressing the issue of low bone formation rates at the center of defects. GL13K was released by approximately 40.87 +/- 4.37 % within the first three days, exerting a localized antibacterial effect and further promoting vascularization and new bone formation in peripheral regions. This design aims to achieve an all-around and efficient bone restoration effect in the extraction socket using coaxial scaffolds through a dual internal and external mechanism.
引用
收藏
页码:97 / 117
页数:21
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