Fabrication and characterization of carboxymethyl cellulose novel microparticles for bone tissue engineering

被引:56
作者
Gaihre, Bipin [1 ]
Jayasuriya, Ambalangodage C. [1 ,2 ]
机构
[1] Univ Toledo, Dept Bioengn, Toledo, OH 43614 USA
[2] Univ Toledo, Dept Orthopaed Surg, Med Ctr, Toledo, OH 43614 USA
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2016年 / 69卷
基金
美国国家卫生研究院;
关键词
Micropartides; Carboxymethyl cellulose; Zirconium; Surface roughness; Pre-osteoblasts; OSTEOBLAST RESPONSE; COMPOSITE SCAFFOLDS; HYDROGEL; DELIVERY; CHITOSAN; CELLS; BIOMATERIALS; RELEASE; STARCH;
D O I
10.1016/j.msec.2016.07.060
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
In this study we developed carboxymethyl cellulose (CMC) microparticles through ionic crosslinking with the aqueous ion complex of zirconium (Zr) and further complexing with chitosan (CS) and determined the physio-chemical and biological properties of these novel microparticles. In order to assess the role of Zr, micro particles were prepared in 5% and 10% (w/v) zirconium tetrachloride solution. Scanning electron microscopy (SEM) with energy dispersive X-ray spectrometer (EDS) results showed that Zr was uniformly distributed on the surface of the microparticles as a result of which uniform groovy surface was obtained. We found that Zr enhances the surface roughness of the microparticles and stability studies showed that it also increases the stability of microparticles in phosphate buffered saline. The crosslinking of anionic CMC with cationic Zr and CS was confirmed by Fourier transform infrared spectroscopy (FTIR) results. The response of murine pre-osteoblasts (OB-6) when cultured with microparticles was investigated. Live/dead cell assay showed that microparticles did not induce any cytotoxic effects as cells were attaching and proliferating on the well plate as well as along the surface of microparticles. In addition, SEM images showed that microparticles support the attachment of cells and they appeared to be directly interacting with the surface of microparticle. Within 10 days of culture most of the top surface of microparticles was covered with a layer of cells indicating that they were proliferating well throughout the surface of microparticles. We observed that Zr enhances the cell attachment and proliferation as more cells were present on microparticles with 10% Zr. These promising results show the potential applications of CMC-Zr micro particles in bone tissue engineering. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:733 / 743
页数:11
相关论文
共 48 条
[1]  
Adair J.H., 1996, MRS ONLINE P LIB ARC, V432
[2]  
[Anonymous], 2013, IOSR J DENT MED SCI
[3]  
[Anonymous], 2015, PLOS ONE
[4]  
Assal Patrick A, 2013, Schweiz Monatsschr Zahnmed, V123, P644
[5]   The effect of different surface morphology and roughness on osteoblast-like cells [J].
Ball, Michael ;
Grant, David M. ;
Lo, Wei-Jen ;
Scotchford, Colin A. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2008, 86A (03) :637-647
[6]   Mechanisms involved in osteoblast response to implant surface morphology [J].
Boyan, BD ;
Lohmann, CH ;
Dean, DD ;
Sylvia, VL ;
Cochran, DL ;
Schwartz, Z .
ANNUAL REVIEW OF MATERIALS RESEARCH, 2001, 31 :357-371
[7]   Microparticles as tissue engineering scaffolds: manufacture, modification and manipulation [J].
Chau, D. Y. S. ;
Agashi, K. ;
Shakesheff, K. M. .
MATERIALS SCIENCE AND TECHNOLOGY, 2008, 24 (09) :1031-1044
[8]   Biodegradable composite scaffolds of bioactive glass/chitosan/carboxymethyl cellulose for hemostatic and bone regeneration [J].
Chen, Chen ;
Li, Hong ;
Pan, Jianfeng ;
Yan, Zuoqin ;
Yao, Zhenjun ;
Fan, Wenshuai ;
Guo, Changan .
BIOTECHNOLOGY LETTERS, 2015, 37 (02) :457-465
[9]   Metallic implant biomaterials [J].
Chen, Qizhi ;
Thouas, George A. .
MATERIALS SCIENCE & ENGINEERING R-REPORTS, 2015, 87 :1-57
[10]   Investigation of potential injectable polymeric biomaterials for bone regeneration [J].
Dreifke, Michael B. ;
Ebraheim, Nabil A. ;
Jayasuriya, Ambalangodage C. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2013, 101 (08) :2436-2447