Tissue responses to novel tissue engineering biodegradable cryogel scaffolds: An animal model

被引:35
作者
Bolgen, Nimet [1 ,2 ]
Vargel, Ibrahim [3 ]
Korkusuz, Petek [4 ]
Guzel, Elif [4 ]
Plieva, Fatima [5 ]
Galaev, Igor [6 ]
Matiasson, Bo [6 ]
Piskin, Erhan [1 ,2 ]
机构
[1] Hacettepe Univ, Dept Chem Engn, TR-06800 Ankara, Turkey
[2] Hacettepe Univ, Bioengn Div, TR-06800 Ankara, Turkey
[3] Kirikkale Univ, Dept Plast & Reconstruct Surg, Fac Med, Kirikkale, Turkey
[4] Hacettepe Univ, Dept Histol & Embryol, Fac Med, TR-06800 Ankara, Turkey
[5] IDEON, Protista Biotechnol AB, SE-22370 Lund, Sweden
[6] Lund Univ, Dept Biotechnol, SE-22100 Lund, Sweden
关键词
tissue-engineering scaffolds; cryogels; biodegradable; HEMA-L-lactide-dextran; animal model; tissue reponses; BONE; BIOCOMPATIBILITY; MATRICES; DEXTRAN; SYSTEM;
D O I
10.1002/jbm.a.32193
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Biodegradable macroporous cryogels with highly open and interconnected pore structures were produced from dextran modified with oligo L-lactide bearing hydroxyethylmethacrylate (HEMA) end groups in moderately frozen solutions. Tissue responses to these novel scaffolds were evaluated in rats after dorsal subcutaneous implantation, iliac submuscular implantation, auricular implantation, or in calvarial defect model. In no case, either necrosis or foreign body reaction was observed during histological studies. The cryogel scaffolds integrated with the surrounding tissue and the formation of a new tissue were accompanied with significant ingrowth of connective tissue cells and new blood vessels into the cryogel. The tissue responses were significantly lower in auricular and calvarial implantations when compared with the subcutanous and the submuscular implantations. The degradation of the scaffold was slower in bone comparing to soft tissues. The biodegradable cryogels are highly biocompatible and combine extraordinary properties including having soft and elastic nature, open porous structure, and very rapid and controllable swelling. Therefore, the cryogels could be promising candidates for further clinical applications in tissue regeneration. (C) 2008 Wiley Periodicals, Inc. J Biomed Mater Res 91 A: 60-68, 2009
引用
收藏
页码:60 / 68
页数:9
相关论文
共 34 条
[1]  
AN YH, 1999, ANIMAL MODELS ORTHOP, P251
[2]   Cryogelation for preparation of novel biodegradable tissue-engineering scaffolds [J].
Boelgen, Nimet ;
Plieva, Fatima ;
Galaev, Igor Yu ;
Mattiasson, Bo ;
Piskin, Erhan .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2007, 18 (09) :1165-1179
[3]   Biomaterial developments for bone tissue engineering [J].
Burg, KJL ;
Porter, S ;
Kellam, JF .
BIOMATERIALS, 2000, 21 (23) :2347-2359
[4]   INVITRO CYTOTOXICITY OF MELANIZED POLY(2-HYDROXYETHYL METHACRYLATE) HYDROGELS, A NOVEL CLASS OF OCULAR BIOMATERIALS [J].
CHIRILA, TV ;
THOMPSON, DE ;
CONSTABLE, IJ .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1992, 3 (06) :481-498
[5]   Biocomposites of non-crosslinked natural and synthetic polymers [J].
Coombes, AGA ;
Verderio, E ;
Shaw, B ;
Li, X ;
Griffin, M ;
Downes, S .
BIOMATERIALS, 2002, 23 (10) :2113-2118
[6]   Cell chromatography: Separation of different microbial cells using IMAC supermacroporous monolithic columns [J].
Dainiak, MB ;
Plieva, FM ;
Galaev, IY ;
Hatti-Kaul, R ;
Mattiasson, B .
BIOTECHNOLOGY PROGRESS, 2005, 21 (02) :644-649
[7]   Integrated isolation of antibody fragments from microbial cell culture fluids using supermacroporous cryogels [J].
Dainiak, MB ;
Kumar, A ;
Plieva, FM ;
Galaev, IY ;
Mattiasson, B .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1045 (1-2) :93-98
[8]  
Fambri L, 2002, INTEGRATED BIOMATERIALS SCIENCE, P119
[9]   BHK cell attachment and growth on EDA-plasma-modified poly(L-lactide/ε-caprolactone) biodegradable films [J].
Gürpinar, ÖA ;
Tuzlakoglu, K ;
Onur, MA ;
Tümer, A ;
Serdar, MA ;
Ünal, N ;
Piskin, E .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2003, 14 (06) :589-600
[10]   Porous polymeric structures for tissue engineering prepared by a coagulation, compression moulding and salt leaching technique [J].
Hou, QP ;
Grijpma, DW ;
Feijen, J .
BIOMATERIALS, 2003, 24 (11) :1937-1947