Incorporation of Calcium Sulfate Dihydrate into Hydroxyapatite Microspheres To Improve the Release of Bone Morphogenetic Protein-2 and Accelerate Bone Regeneration

被引:16
作者
Baek, Jaeuk [1 ]
Lee, Hyun [1 ]
Jang, Tae-Sik [2 ]
Song, Juha [2 ]
Kim, Hyoun-Ee [1 ,3 ]
Jung, Hyun-Do [4 ]
机构
[1] Seoul Natl Univ, Dept Mat Sci & Engn, Seoul 151742, South Korea
[2] Nanyang Technol Univ, Chem & Biomed Engn, 70 Nanyang Dr, Singapore 637457, Singapore
[3] Adv Inst Convergence Technol, Biomed Implant Convergence Res Ctr, Suwon 443270, South Korea
[4] Korea Inst Ind Technol, Liquid Proc & Casting Technol R&D Grp, Incheon 21999, South Korea
基金
新加坡国家研究基金会;
关键词
hydroxyapatite microspheres; bone morphogenetic protein; bone regeneration; calcium sulfate dihydrate; in vivo animal test; IN-VIVO; PHOSPHATE CEMENTS; DRUG-DELIVERY; IMPLANTS; SCAFFOLD; DEFECTS; TISSUE; DIFFERENTIATION; PROLIFERATION; ARCHITECTURE;
D O I
10.1021/acsbiomaterials.7b00715
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
082905 [生物质能源与材料]; 100103 [病原生物学];
摘要
In this study, hydroxyapatite (HA)-based microspheres with the ability to deliver bone morphogenetic protein-2 (BMP-2) were developed for accelerating bone regeneration. The incorporation of calcium sulfate dihydrate (CSD) in the HA matrix improved the rate of BMP-2 release from the microspheres. Under physiological conditions, the CSD fully degraded within 7 days and generated pore channels in the microspheres. The porosity and pore size of the HA-CSD microspheres after CSD degradation were 34.3% +/- 4.2% and 11.5 +/- 2.4 mu m, respectively, significantly larger than those of the HA microspheres (23.9% +/- 3.1% and 8.7 +/- 0.9 mu m, respectively). The increased porosity directly affected the rate of BMP-2 release from the microspheres. An in vitro experiment showed that both the BMP-2 release rate and the total amount of BMP-2 released increased considerably when incorporating the HA microspheres with CSD. BMP-2 was released slowly from the HA microspheres for up to 6 weeks. BMP-2 release was notably improved in the HA-CSD biphasic microspheres compared to the microspheres without CSD; the rate of release was 2.4-times faster due to the pores created by CSD dissolution after 7 days. Prior to animal testing, in vitro cell tests were performed to evaluate the biocompatibility of the HA-CSD microspheres. During CSD dissolution, biocompatible bone-like apatite precipitated on the cell surfaces, and preosteoblasts grew on the microspheres. In vivo experiments using a rabbit lateral femoral condyle defect model demonstrated that the level of bone regeneration was significantly enhanced by mineralization on the surface, generated additional pores as well as improved BMP-2 release behavior. The HA-CSD microspheres accelerated new bone growth to fill the entire defect in 6 weeks, corresponding to a 170% improvement in performance compared to the HA microspheres.
引用
收藏
页码:846 / 856
页数:21
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