Preparation and characterization of RGD-immobilized chitosan scaffolds

被引:164
作者
Ho, MH
Wang, DM
Hsieh, HJ
Liu, HC
Hsien, TY
Lai, JY
Hou, LT
机构
[1] Natl Taiwan Univ, Dept Chem Engn, Taipei 10764, Taiwan
[2] Natl Taiwan Univ, Inst Biomed Engn, Taipei 10764, Taiwan
[3] Chung Kuo Inst Technol, Gen Educ Ctr, Taipei, Taiwan
[4] R&D Ctr Membrane Technol, Chungli, Taiwan
[5] Dept Chem Engn, Chungli, Taiwan
[6] Natl Taiwan Univ, Sch Dent, Grad Inst Clin Dent, Taipei 10764, Taiwan
[7] Natl Taiwan Univ Hosp, Dept Periodontol, Taipei, Taiwan
关键词
chitosan; scaffold; RGD; tissue engineering; bone regeneration; biocompatibility;
D O I
10.1016/j.biomaterials.2004.08.032
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Chitosan scaffolds were modified with RGDS (Arg-Gly-Asp-Ser) in the present work via an imide-bond forming reaction between amino groups in chitosan and carboxyl groups in peptides. Successful immobilization was verified with FTIR spectroscopy, and the immobilized amount was determined to be on the order of 10(-12) Mol/cm(2) through analysis of the immobilized amino acids. Results of experiments of cell culture with rat osteosarcoma (ROS) cells demonstrated that RGDS immobilization could enhance the attachment of ROS cells onto the chitosan, resulting in higher cell density attached to the RGDS-modified scaffold than to the unmodified scaffold. It should be noted that only RGDS, but not other peptide such as RGES, is effective in enhancing cell attachment and possible proliferation. Experiments of in vitro mineralization indicated that there were more cells on the RGDS-modified scaffold than on the unmodified scaffold, which tended to form bone-like tissues. The results presented in this work suggest that immobilization of RGDS can make chitosan scaffolds more compatible for the culture of osteoblast-like cells and the regeneration of bone-like tissues. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3197 / 3206
页数:10
相关论文
共 39 条
  • [21] Endothelial cell migration on surfaces modified with immobilized adhesive peptides
    Kouvroukoglou, S
    Dee, KC
    Bizios, R
    McIntire, LV
    Zygourakis, K
    [J]. BIOMATERIALS, 2000, 21 (17) : 1725 - 1733
  • [22] TISSUE ENGINEERING
    LANGER, R
    VACANTI, JP
    [J]. SCIENCE, 1993, 260 (5110) : 920 - 926
  • [23] COVALENT SURFACE IMMOBILIZATION OF ARG-GLY-ASP-CONTAINING AND TYR-ILE-GLY-SER-ARG-CONTAINING PEPTIDES TO OBTAIN WELL-DEFINED CELL-ADHESIVE SUBSTRATES
    MASSIA, SP
    HUBBELL, JA
    [J]. ANALYTICAL BIOCHEMISTRY, 1990, 187 (02) : 292 - 301
  • [24] AN RGD SPACING OF 440NM IS SUFFICIENT FOR INTEGRIN ALPHA-V-BETA-3-MEDIATED FIBROBLAST SPREADING AND 140NM FOR FOCAL CONTACT AND STRESS FIBER FORMATION
    MASSIA, SP
    HUBBELL, JA
    [J]. JOURNAL OF CELL BIOLOGY, 1991, 114 (05) : 1089 - 1100
  • [25] PREVASCULARIZATION OF POROUS BIODEGRADABLE POLYMERS
    MIKOS, AG
    SARAKINOS, G
    LYMAN, MD
    INGBER, DE
    VACANTI, JP
    LANGER, R
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 1993, 42 (06) : 716 - 723
  • [26] MOONEY DJ, 1994, TRANSPLANT P, V26, P3425
  • [27] BIODEGRADABLE SPONGES FOR HEPATOCYTE TRANSPLANTATION
    MOONEY, DJ
    PARK, S
    KAUFMANN, PM
    SANO, K
    MCNAMARA, K
    VACANTI, JP
    LANGER, R
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1995, 29 (08): : 959 - 965
  • [28] OGUNTIMEIN GB, 1980, BIOTECHNOL BIOENG, V12, P1127
  • [29] Poly(L-lysine)-GRGDS as a biomimetic surface modifier for poly(lactic acid)
    Quirk, RA
    Chan, WC
    Davies, MC
    Tendler, SJB
    Shakesheff, KM
    [J]. BIOMATERIALS, 2001, 22 (08) : 865 - 872
  • [30] Human microvascular endothelial cell growth and migration on biomimetic surfactant polymers
    Sagnella, SM
    Kligman, F
    Anderson, EH
    King, JE
    Murugesan, G
    Marchant, RE
    Kottke-Marchant, K
    [J]. BIOMATERIALS, 2004, 25 (7-8) : 1249 - 1259