Preparation, structure and crystallinity of chitosan nano-fibers by a solid-liquid phase separation technique

被引:126
作者
Zhao, Jianhao [1 ,2 ]
Han, Wanqing [1 ]
Chen, Haodong [1 ]
Tu, Mei [1 ,2 ]
Zeng, Rong [1 ,2 ]
Shi, Yunfeng [3 ]
Cha, Zhengang [2 ,4 ]
Zhou, Changren [1 ,2 ]
机构
[1] Jinan Univ, Dept Mat Sci & Engn, Coll Sci & Engn, Guangzhou 510632, Guangdong, Peoples R China
[2] Minist Educ, Engn Res Ctr Artificial Organs & Mat, Guangzhou 510632, Guangdong, Peoples R China
[3] Jinan Univ, Anal & Test Ctr, Guangzhou 510632, Guangdong, Peoples R China
[4] Jinan Univ, Hosp 1, Dept Orthopaed, Guangzhou 510632, Guangdong, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
Chitosan; Nano-fibrous; Solid-liquid phase separation; Structure; Crystallinity; NANOFIBROUS SCAFFOLDS; STEM-CELLS; ARCHITECTURE; MATRICES;
D O I
10.1016/j.carbpol.2010.10.009
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Chitosan acetate nano-fibers were fabricated via a solid-liquid phase separation technique. The chitosan acetate structure was influenced by phase separation temperature, chitosan concentration and acetic acid concentration. Uniform nano-fibrous chitosan acetate of 50-500 nm in diameter was engineered at 0.05% (w/v)chitosan and 0.025% (v/v) acetic acid in liquid nitrogen, as opposed to film-shape and micro-fibrous structure at -18 degrees C and -80 degrees C respectively. Decreasing the chitosan concentration led to the formation of nano-fibrous/floccules-like structure, while increasing the acetic acid concentration resulted in nano-/micro-fibrous structure instead. The chitosan acetate structure was closely related to the crystallinity varying with different phase separation conditions. Nano-fibrous chitosan acetate showed a medium crystallinity with a glass transition temperature of 155.1 degrees C and a heat capacity of 29.1 J/g comparing with nano-fibrous/floccules-like and nano-/micro-fibrous samples. The chitosan acetate crystal was also found changeable from form I to form II after solid-liquid phase separation in liquid nitrogen. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1541 / 1546
页数:6
相关论文
共 31 条
[1]   Self-assembling peptide amphiphile nanofiber matrices for cell entrapment [J].
Beniash, E ;
Hartgerink, JD ;
Storrie, H ;
Stendahl, JC ;
Stupp, SI .
ACTA BIOMATERIALIA, 2005, 1 (04) :387-397
[2]   Electrospun chitosan-based nanofibers and their cellular compatibility [J].
Bhattarai, N ;
Edmondson, D ;
Veiseh, O ;
Matsen, FA ;
Zhang, MQ .
BIOMATERIALS, 2005, 26 (31) :6176-6184
[3]   Crystallization of polymers at constant and high cooling rates: A new hot-stage microscopy set-up [J].
Boyer, S. A. E. ;
Haudin, J. -M .
POLYMER TESTING, 2010, 29 (04) :445-452
[4]   Nano-fibrous poly(L-lactic acid) scaffolds with interconnected spherical macropores [J].
Chen, VJ ;
Ma, PX .
BIOMATERIALS, 2004, 25 (11) :2065-2073
[5]   Studies on glass transition temperature of chitosan with four techniques [J].
Dong, YM ;
Ruan, YH ;
Wang, HW ;
Zhao, YG ;
Bi, DX .
JOURNAL OF APPLIED POLYMER SCIENCE, 2004, 93 (04) :1553-1558
[6]   COLLAGEN SUBSTRATA FOR STUDIES ON CELL BEHAVIOR [J].
ELSDALE, T ;
BARD, J .
JOURNAL OF CELL BIOLOGY, 1972, 54 (03) :626-&
[7]  
Hay E. D., 1991, CELL BIOL EXTRACELLU
[8]   Fabrication and characterization of poly(L-lactic acid) 3D nanofibrous scaffolds with controlled architecture by liquid-liquid phase separation from a ternary polymer-solvent system [J].
He, Liumin ;
Zhang, Yanqing ;
Zeng, Xiang ;
Quan, Daping ;
Liao, Susan ;
Zeng, Yuanshan ;
Lu, Jiang ;
Ramakrishna, S. .
POLYMER, 2009, 50 (16) :4128-4138
[9]   Chondrogenic and osteogenic differentiations of human bone marrow-derived mesenchymal stem cells on a nanofibrous scaffold with designed pore network [J].
Hu, Jiang ;
Feng, Kai ;
Liu, Xiaohua ;
Ma, Peter X. .
BIOMATERIALS, 2009, 30 (28) :5061-5067
[10]   Nanofibrous polyhydroxyalkanoate matrices as cell growth supporting materials [J].
Li, Xiao-Tao ;
Zhang, Yan ;
Chen, Guo-Qiang .
BIOMATERIALS, 2008, 29 (27) :3720-3728