Preparation of chitosan-gelatin hybrid scaffolds with well-organized microstructures for hepatic tissue engineering

被引:156
作者
He Jiankang [1 ]
Li Dichen [1 ]
Liu Yaxiong [1 ]
Yao Bo [1 ]
Zhan Hanxiang [2 ]
Lian Qin [1 ]
Lu Bingheng [1 ]
Lv Yi [2 ]
机构
[1] Xi An Jiao Tong Univ, State Key Lab Mfg Syst Engn, Xian 710049, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Coll Med, Xian 710061, Shaanxi, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
Chitosan-gelatin; Porous; Well organized; Scaffold; Hepatocyte; COLLAGEN SCAFFOLD; FABRICATION; CULTURE; HEPATOCYTES; HYDROXYAPATITE;
D O I
10.1016/j.actbio.2008.07.002
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The structural organization of natural liver is instrumental in the multi functionality of hepatocytes, and mimicking these specific architectures in tissue-engineered scaffold plays an important role in the engineering of an implantable liver equivalent in vitro. To achieve this goal, we have developed a novel fabrication process to create chitosan-gelatin hybrid scaffolds with well-organized architectures and highly porous structures by combining rapid prototyping, microreplication and freeze-drying techniques. The scaffolds obtained not only have analogous configurations of portal vein, central vein, flow-channel network and hepatic chambers, but also have high (>90%) porosity, with the mean pore size of 100 mu m. Swelling and degradation studies showed that the scaffold has excellent properties of hydrophilicity and biodegradability. A hepatocyte culture experiment was conducted to evaluate the efficiency of the well-defined chitosan-gelatin scaffold in facilitating hepatocyte growth in the inner layer of the scaffold in vitro. Scanning electron microscopy and histological analysis showed that hepatocytes could form large colonies in the predefined hepatic chambers, and these cavities could the completely filled with hepatocytes during 7 day culture. Albumin secretion and urea synthesis further indicated that the well-organized scaffolds were more suitable for hepatocyte culture. (C) 2008 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:453 / 461
页数:9
相关论文
共 39 条
[1]   Investigation of the mechanical properties and porosity relationships in fused deposition modelling-fabricated porous structures [J].
Ang, Ker Chin ;
Leong, Kah Fai ;
Chua, Chee Kai ;
Chandrasekaran, Margam .
RAPID PROTOTYPING JOURNAL, 2006, 12 (02) :100-105
[2]   Three-dimensional microfluidic tissue-engineering scaffolds using a flexible biodegradable polymer [J].
Bettinger, CJ ;
Weinberg, EJ ;
Kulig, KM ;
Vacanti, JP ;
Wang, YD ;
Borenstein, JT ;
Langer, R .
ADVANCED MATERIALS, 2006, 18 (02) :165-+
[3]   Study on physical properties and nerve cell affinity of composite films from chitosan and gelatin solutions [J].
Cheng, MY ;
Deng, JU ;
Yang, F ;
Gong, YD ;
Zhao, NM ;
Zhang, XF .
BIOMATERIALS, 2003, 24 (17) :2871-2880
[4]  
Elcin YM, 1998, ARTIF ORGANS, V22, P837
[5]   Endothelialized microvasculature based on a biodegradable elastomer [J].
Fidkowski, C ;
Kaazempur-Mofrad, MR ;
Borenstein, J ;
Vacanti, JP ;
Langer, R ;
Wang, YD .
TISSUE ENGINEERING, 2005, 11 (1-2) :302-309
[6]   Fabrication and characterization of chitosan/gelatin porous scaffolds with predefined internal microstructures [J].
He Jiankang ;
Li Dichen ;
Liu Yaxiong ;
Yao Bo ;
Lu Bingheng ;
Lian Qin .
POLYMER, 2007, 48 (15) :4578-4588
[7]   Avidin-biotin binding-based cell seeding and perfusion culture of liver-derived cells in a porous scaffold with a three-dimensional interconnected flow-channel network [J].
Huang, Hongyun ;
Oizumi, Shunsuke ;
Kojima, Nobuhiko ;
Niino, Toshiki ;
Sakai, Yasuyuki .
BIOMATERIALS, 2007, 28 (26) :3815-3823
[8]   Building structure into engineered tissues [J].
Isenberg, Brett C. ;
Wong, Joyce Y. .
MATERIALS TODAY, 2006, 9 (12) :54-60
[9]   Highly porous polymer matrices as a three-dimensional culture system for hepatocytes [J].
Kaufmann, PM ;
Heimrath, S ;
Kim, BS ;
Mooney, DJ .
CELL TRANSPLANTATION, 1997, 6 (05) :463-468
[10]  
KHANNA HJ, 2000, ANN INT C IEEE ENG M, V2, P1259