Preparation and characterization of dexamethasone-immobilized chitosan scaffold

被引:24
作者
Chiang, Zu-Chian [1 ]
Yu, Shu-Huei [2 ]
Chao, An-Chong [1 ]
Dong, Guo-Chung [1 ,3 ]
机构
[1] Natl United Univ, Dept Chem Engn, Miaoli 36003, Taiwan
[2] Vanung Univ, Dept Polymer Mat, Tao Yuan 32061, Taiwan
[3] Natl Hlth Res Inst, Div Med Engn Res, Miaoli 35035, Taiwan
关键词
Chitosan; Dexamethasone; Immobilization; AD-MSCs; Cell images; BONE MORPHOGENETIC PROTEIN-2; IN-VITRO; OSTEOGENIC DIFFERENTIATION; OSTEOBLAST PHENOTYPE; COMPOSITE SCAFFOLDS; CELLS; TITANIUM; ATTACHMENT; HYDROGELS; ENHANCE;
D O I
10.1016/j.jbiosc.2012.01.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chitosan film (CSF), 2-dimensional scaffold, was modified with dexamethasone (DEX) in the present work via amino-alcohol forming reaction between amino group of chitosan and carbonyl group of DEX. Successful immobilization was identified by ATR-FTIR spectroscopy and, the immobilized amounts were determined by weighting methods (WM) and integrated area analysis method (AM) of HPLC. For experiments of cell culture of osteogenic differentiation, our results showed that DEX immobilization has more efficiency than the other group (such as both groups of CSF and CSF with free DEX, CSF/fDEX), which was demonstrated as indicated by cell image analysis and ALP activity assay. The results show, as AD-MSCs cultured on DEX-CSF, its shape of cell transformed to polygonal or cubical. The ALP activity assay indicates that of DEX-CSF increase about 3.5 folds than that of CSFs. The results suggest that immobilization of DEX can make chitosan scaffolds to induce differentiation of AD-MSCs toward osteoblastic lineage for bone tissue engineering application. (C) 2012, The Society for Biotechnology, Japan. All rights reserved.
引用
收藏
页码:654 / 660
页数:7
相关论文
共 36 条
[1]   INTEGRINS AND OTHER CELL-ADHESION MOLECULES [J].
ALBELDA, SM ;
BUCK, CA .
FASEB JOURNAL, 1990, 4 (11) :2868-2880
[2]   THE EFFECTS OF DEXAMETHASONE AND 1,25-DIHYDROXYVITAMIN D-3 ON OSTEOGENIC DIFFERENTIATION OF HUMAN MARROW STROMAL CELLS IN-VITRO [J].
BERESFORD, JN ;
JOYNER, CJ ;
DEVLIN, C ;
TRIFFITT, JT .
ARCHIVES OF ORAL BIOLOGY, 1994, 39 (11) :941-947
[3]   Photoencapsulation of osteoblasts in injectable RGD-modified PEG hydrogels for bone tissue engineering [J].
Burdick, JA ;
Anseth, KS .
BIOMATERIALS, 2002, 23 (22) :4315-4323
[4]   DIFFERENTIATION OF HUMAN BONE-MARROW OSTEOGENIC STROMAL CELLS IN VITRO - INDUCTION OF THE OSTEOBLAST PHENOTYPE BY DEXAMETHASONE [J].
CHENG, SL ;
YANG, JW ;
RIFAS, L ;
ZHANG, SF ;
AVIOLI, LV .
ENDOCRINOLOGY, 1994, 134 (01) :277-286
[5]   Characterization of the morphology and hydrophilicity of chitosan/caffeic acid hybrid scaffolds [J].
Chiang, Zu-Chian ;
Li, Hsing-Ya ;
Chao, An-Chong ;
Su, Yu-Ru .
JOURNAL OF POLYMER RESEARCH, 2011, 18 (06) :2205-2212
[6]   Growth of human endothelial cells on photochemically grafted Gly-Arg-Gly-Asp (GRGD) chitosans [J].
Chung, TW ;
Lu, YF ;
Wang, SS ;
Lin, YS ;
Chu, SH .
BIOMATERIALS, 2002, 23 (24) :4803-4809
[7]  
Gomes M, 2008, ACAD PR SER BIOM ENG, P145, DOI 10.1016/B978-0-12-370869-4.00006-9
[8]   Preparation and characterization of RGD-immobilized chitosan scaffolds [J].
Ho, MH ;
Wang, DM ;
Hsieh, HJ ;
Liu, HC ;
Hsien, TY ;
Lai, JY ;
Hou, LT .
BIOMATERIALS, 2005, 26 (16) :3197-3206
[9]   Preparation and characterization of biodegradable chitosan/hydroxyapatite nanocomposite rods via in situ hybridization: A potential material as internal fixation of bone fracture [J].
Hu, QL ;
Li, BQ ;
Wang, M ;
Shen, JC .
BIOMATERIALS, 2004, 25 (05) :779-785
[10]   Porous polymer scaffolds surface-modified with arginine-glycine-aspartic acid enhance bone cell attachment and differentiation in vitro [J].
Hu, YH ;
Winn, SR ;
Krajbich, I ;
Hollinger, JO .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2003, 64A (03) :583-590