Photocurable 3D-printed PMBG/TCP biphasic scaffold mimicking vasculature for bone regeneration

被引:4
|
作者
Zhang, Changru [1 ,2 ,3 ]
Ren, Ya [1 ,2 ]
Kong, Weiqing [2 ,4 ]
Liu, Yihao [2 ]
Li, Heyue [5 ]
Yang, Han [2 ]
Cai, Bin [6 ]
Dai, Kerong [1 ,2 ]
Wang, Chengwei [2 ]
Tang, Liang [7 ]
Niu, Haoyi [2 ]
Wang, Jinwu [1 ,2 ]
机构
[1] Southwest JiaoTong Univ, Coll Med, 11 North 1st Sect Second Ring Road, Chengdu 610036, Peoples R China
[2] Shanghai Jiao Tong Univ, Dept Orthopaed Surg, Shanghai Key Lab Orthopaed Implant, Shanghai Ninth Peoples Hosp Affiliated,Sch Med, 639 Zhizaoju Rd, Shanghai 200011, Peoples R China
[3] Shanghai Jiao Tong Univ, Inst Translat Med, 800 Dongchuan Rd, Qingdao 266000, Shandong, Peoples R China
[4] Qingdao Univ, Affiliated Hosp, Dept Spinal Surg, 59 Haier Rd, Qingdao 266000, Shandong, Peoples R China
[5] Shanghai Univ Tradit Chinese Med, Shanghai Peoples Hosp 7, Obstet & Gynecol, 358 Datong Rd, Shanghai 200137, Peoples R China
[6] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Dept Rehabil Med, Sch Med, 500 Quxi Rd, Shanghai 200011, Peoples R China
[7] Shanghai Jiao Tong Univ, Tongren Hosp, Dept Orthoped Surg, Sch Med, 1111 XianXia Rd, Shanghai 200336, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocurable mesoporous bioglass; Personalization; Bone repair; Angiogenesis; PROMOTES;
D O I
10.18063/ijb.767
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Mesoporous bioglass (MBG) with excellent osteointegration, osteoinduction, and biodegradability is a promising material for bone regeneration. However, its clinical application is hindered by complex processing and a lack of personalization, low mechanical strength, and uncontrollable degradation rate. In this study, we developed a double-bond-functionalized photocurable mesoporous bioglass (PMBG) sol that enabled ultrafast photopolymerization within 5 s. By further integrating nanosized tricalcium phosphate (TCP) particles through three-dimensional (3D) printing technology, we fabricated personalized and highly porous PMBG/TCP biphasic scaffolds. The mechanical properties and degradation behavior of the scaffolds were regulated by varying the amount of TCP doping. In vitro and in vivo experiments verified that PMBG/TCP scaffolds slowly released SiOa and Ca2+, forming a vascularized bone regeneration microenvironment within the fully interconnected pore channels of the scaffold. This microenvironment promoted angiogenesis and accelerated bone tissue regeneration. Overall, this work demonstrates the solution to the problem of complex processing and lack of personalization in bioglass scaffolds, and the developed PMBG/TCP biphasic scaffold is an ideal material for bone regeneration applications with broad clinical prospects.
引用
收藏
页码:369 / 386
页数:18
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