Enhanced biocompatibility and osteogenic potential of mesoporous magnesium silicate/polycaprolactone/wheat protein composite scaffolds

被引:26
作者
Kang, Yun Gyeong [1 ]
Wei, Jie [2 ]
Shin, Ji Won [1 ]
Wu, Yan Ru [3 ]
Su, Jiacan [4 ]
Park, Young Shik [5 ]
Shin, Jung-Woog [1 ,3 ,6 ]
机构
[1] Inje Univ, Sch Biomed Engn, Gimhae, South Korea
[2] East China Univ Sci & Technol, Minist Educ, Key Lab Ultrafine Mat, Shanghai, Peoples R China
[3] Inje Univ, Dept Hlth Sci & Technol, Gimhae, South Korea
[4] Second Mil Med Univ, Changhai Hosp, Dept Orthopaed, Shanghai, Peoples R China
[5] Inje Univ, Sch Biol Sci, Gimhae, South Korea
[6] Inje Univ, UHARC, Inst Aged Life Redesign, Cardiovasc & Metab Dis Ctr, Gimhae, South Korea
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2018年 / 13卷
基金
新加坡国家研究基金会;
关键词
mesoporous magnesium silicate; wheat protein; scaffold; bone tissue engineering; osteogenic differentiation; MARROW STROMAL CELLS; TISSUE ENGINEERING APPLICATIONS; IN-VITRO; SURFACE MODIFICATION; DRUG-DELIVERY; HUMAN BONE; PORE-SIZE; POLYCAPROLACTONE; DEGRADATION; CYTOCOMPATIBILITY;
D O I
10.2147/IJN.S157921
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: Successful bone tissue engineering using scaffolds is primarily dependent on the properties of the scaffold, including biocompatibility, highly interconnected porosity, and mechanical integrity. Methods: In this study, we propose new composite scaffolds consisting of mesoporous magnesium silicate (m_MS), polycaprolactone (PCL), and wheat protein (WP) manufactured by a rapid prototyping technique to provide a micro/macro porous structure. Experimental groups were set based on the component ratio: (1) WP0% (m_MS: PCL: WP=30: 70: 0 weight per weight; w/w); (2) WP15% (m_MS: PCL: WP=30: 55: 15 w/w); (3) WP30% (m_MS: PCL: WP=30: 40: 30 w/w). Results: Evaluation of the properties of fabricated scaffolds indicated that increasing the amount of WP improved the surface hydrophilicity and biodegradability of m_MS/PCL/WP composites, while reducing the mechanical strength. Moreover, experiments were performed to confirm the biocompatibility and osteogenic differentiation of human mesenchymal stem cells (MSCs) according to the component ratio of the scaffold. The results confirmed that the content of WP affects proliferation and osteogenic differentiation of MSCs. Based on the last day of the experiment, ie, the 14th day, the proliferation based on the amount of DNA was the best in the WP30% group, but all of the markers measured by PCR were the most expressed in the WP15% group. Conclusion: These results suggest that the m_MS/PCL/WP composite is a promising candidate for use as a scaffold in cell-based bone regeneration.
引用
收藏
页码:1107 / 1117
页数:11
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共 46 条
  • [41] Clinoenstatite coatings have high bonding strength, bioactive ion release, and osteoimmunomodulatory effects that enhance in vivo osseointegration
    Wu, Chengtie
    Chen, Zetao
    Wu, Qianju
    Yi, Deliang
    Friis, Thor
    Zheng, Xuebin
    Chang, Jiang
    Jiang, Xinquan
    Xiao, Yin
    [J]. BIOMATERIALS, 2015, 71 : 35 - 47
  • [42] Rapid prototyping in tissue engineering: challenges and potential
    Yeong, WY
    Chua, CK
    Leong, KF
    Chandrasekaran, M
    [J]. TRENDS IN BIOTECHNOLOGY, 2004, 22 (12) : 643 - 652
  • [43] Magnesium ion stimulation of bone marrow stromal cells enhances osteogenic activity, simulating the effect of magnesium alloy degradation
    Yoshizawa, Sayuri
    Brown, Andrew
    Barchowsky, Aaron
    Sfeir, Charles
    [J]. ACTA BIOMATERIALIA, 2014, 10 (06) : 2834 - 2842
  • [44] Progress and challenge for magnesium alloys as biomaterials
    Zeng, Rongchang
    Dietzel, Wolfgang
    Witte, Frank
    Hort, Norbert
    Blawert, Carsten
    [J]. ADVANCED ENGINEERING MATERIALS, 2008, 10 (08) : B3 - B14
  • [45] Surface modification of polycaprolactone membrane via aminolysis and biomacromolecule immobilization for promoting cytocompatibility of human endothelial cells
    Zhu, YB
    Gao, CY
    Liu, XY
    Shen, JC
    [J]. BIOMACROMOLECULES, 2002, 3 (06) : 1312 - 1319
  • [46] Surface modification of polycaprolactone with poly(methacrylic acid) and gelatin covalent immobilization for promoting its cytocompatibility
    Zhu, YB
    Gao, CY
    Shen, JC
    [J]. BIOMATERIALS, 2002, 23 (24) : 4889 - 4895