The use of injectable sonication-induced silk hydrogel for VEGF165 and BMP-2 delivery for elevation of the maxillary sinus floor

被引:322
作者
Zhang, Wenjie [2 ]
Wang, Xiuli [3 ,4 ]
Wang, Shaoyi [5 ]
Zhao, Jun [5 ]
Xu, Lianyi [2 ]
Zhu, Chao [5 ]
Zeng, Deliang [2 ]
Chen, Jake [6 ]
Zhang, Zhiyuan [5 ]
Kaplan, David L. [4 ]
Jiang, Xinquan [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Peoples Hosp 9, Sch Med, Dept Prosthodont, Shanghai 200011, Peoples R China
[2] Shanghai Jiao Tong Univ, Oral Bioengn & Regenerat Med Lab, Shanghai Res Inst Stomatol, Sch Med,Shanghai Key Lab Stomatol,Peoples Hosp 9, Shanghai 200011, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem & Phys, Dalian 116023, Peoples R China
[4] Tufts Univ, Dept Biomed Engn, Sch Engn, Medford, MA 02155 USA
[5] Shanghai Jiao Tong Univ, Sch Med, Dept Oral & Maxillofacial Surg, Peoples Hosp 9, Shanghai 200011, Peoples R China
[6] Tufts Univ, Sch Dent Med, Div Oral Biol, Boston, MA 02111 USA
基金
中国国家自然科学基金;
关键词
Silk fibron; Hydrogels; Sonication; VEGF; BMP-2; Maxillary sinus augmentation; BONE MORPHOGENETIC PROTEIN-2; TISSUE-ENGINEERED BONE; IN-VIVO; FIBROIN SCAFFOLDS; AUGMENTATION; REPAIR; VEGF; BIOMATERIALS; ANGIOGENESIS; REGENERATION;
D O I
10.1016/j.biomaterials.2011.08.047
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Sonication-induced silk hydrogels were previously prepared as an injectable bone replacement biomaterial, with a need to improve osteogenic features. Vascular endothelial growth factor (VEGF(165)) and bone morphogenic protein-2 (BMP-2) are key regulators of angiogenesis and osteogenesis, respectively, during bone regeneration. Therefore, the present study aimed at evaluating in situ forming silk hydrogels as a vehicle to encapsulate dual factors for rabbit maxillary sinus floor augmentation. Sonication-induced silk hydrogels were prepared in vitro and the slow release of VEGF(165) and BMP-2 from these silk gels was evaluated by ELISA. For in vivo studies for each time point (4 and 12 weeks), 24 sinus floors elevation surgeries were made bilaterally in 12 rabbits for the following four treatment groups: silk gel (group Silk gel), silk gel/VEGF(165) (group VEGF), silk gel/BMP-2 (group BMP-2), silk gel/VEGF(165)/BMP-2 (group V + B) (n = 6 per group). Sequential florescent labeling and radiographic observations were used to record new bone formation and mineralization, along with histological and histomorphometric analysis. At week 4, VEGF(165) promoted more tissue infiltration into the gel and accelerated the degradation of the gel material. At this time point, the bone area in group V + B was significantly larger than those in the other three groups. At week 12, elevated sinus floor heights of groups BMP-2 and V + B were larger than those of the Silk gel and VEGF groups, and the V + B group had the largest new bone area among all groups. In addition, a larger blood vessel area formed in the remaining gel areas in groups VEGF and V + B. In conclusion, VEGF(165) and BMP-2 released from injectable and biodegradable silk gels promoted angiogenesis and new bone formation, with the two factors demonstrating an additive effect on bone regeneration. These results indicate that silk hydrogels can be used as an injectable vehicle to deliver multiple growth factors in a minimally invasive approach to regenerate irregular bony cavities. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9415 / 9424
页数:10
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