Structure-property relations and cytotoxicity of isosorbide-based biodegradable polyurethane scaffolds for tissue repair and regeneration

被引:48
作者
Gogolewski, Sylwester [1 ]
Gorna, Katarzyna [1 ]
Zaczynska, Ewa [2 ]
Czary, Anna [2 ]
机构
[1] AO Res Inst, CH-7270 Davos, Switzerland
[2] Polish Acad Sci, Inst Immunol & Expt Therapy, PL-53114 Wroclaw, Poland
关键词
biodegradable polyurethane; porous scaffolds; structure-property relations; MTT cytotoxicity assay; proinflammatory cytokines;
D O I
10.1002/jbm.a.31481
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Microporous scaffolds with potential applications for tissue engineering were produced from the biodegradable aliphatic isosorbide-based polyurethane using a combined salt leaching-solvent evaporation-coagulation process. Alkaline sodium phosphate heptahydrate crystals were used as a solid porogene, and acetone-water mixture was used as a nonsolvent-coagulant. The scaffolds used in this study had interconnected pores with sizes in the range of 70-120 mu m and a pore-to-volume ratio of 87%. The XPS measurements showed that the residence of the scaffold in an aqueous solution of the alkaline porogene changed its surface atomic composition, that is increased the surface concentration of oxygen and nitrogen and reduced the surface concentration of hydrocarbons relative to the control material. This also enhanced the hydrophilicity of the scaffold's surfaces as assessed from contact angle measurements. The alkaline porogene did not affect the polymer's molecular weight. The MTT cytotoxicity assay showed that the isosorbide-based polyurethane scaffold is noncytotoxic. The amounts of interleukin-6 and interlukin-8 proinflammatory cytokines released from human blood leukocytes exposed to the polyurethane scaffolds in vitro were comparable and/or lower than the amount of the cytokines released by leukocytes exposed to the culture-grade polystyrene control. (C) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:456 / 465
页数:10
相关论文
共 29 条
[1]
Host response to tissue engineered devices [J].
Babensee, JE ;
Anderson, JM ;
McIntire, LV ;
Mikos, AG .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 33 (1-2) :111-139
[2]
In vivo leukocyte cytokine mRNA responses to biomaterials are dependent on surface chemistry [J].
Brodbeck, WG ;
Voskerician, G ;
Ziats, NP ;
Nakayama, Y ;
Matsuda, T ;
Anderson, JM .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2003, 64A (02) :320-329
[3]
Biomaterial adherent macrophage apoptosis is increased by hydrophilic and anionic substrates in vivo [J].
Brodbeck, WG ;
Patel, J ;
Voskerician, G ;
Christenson, E ;
Shive, MS ;
Nakayama, Y ;
Matsuda, T ;
Ziats, NP ;
Anderson, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10287-10292
[4]
BROWN L, 2003, POLYURETHANE MEMBRAN
[5]
INVITRO LEUKOCYTE ADHESION TO MODIFIED POLYURETHANE SURFACES .1. EFFECT OF IONIZABLE FUNCTIONAL-GROUPS [J].
BRUIL, A ;
TERLINGEN, JGA ;
BEUGELING, T ;
VANAKEN, WG ;
FEIJEN, J .
BIOMATERIALS, 1992, 13 (13) :915-923
[6]
INVIVO LEUKOCYTE INTERACTIONS ON PELLETHANE SURFACES [J].
BRUNSTEDT, MR ;
ANDERSON, JM ;
SPILIZEWSKI, KL ;
MARCHANT, RE ;
HILTNER, A .
BIOMATERIALS, 1990, 11 (06) :370-378
[7]
Cytotoxicity testing of endodontic sealers: A new method [J].
Camps, J ;
About, I .
JOURNAL OF ENDODONTICS, 2003, 29 (09) :583-586
[8]
CASTNER D G, 1990, Journal of Biomaterials Science Polymer Edition, V1, P191
[9]
Surface chemistry mediates adhesive structure, cytoskeletal organization, and fusion of macrophages [J].
Dadsetan, M ;
Jones, JA ;
Hiltner, A ;
Anderson, JM .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2004, 71A (03) :439-448
[10]
Correlation of cytokine elaboration with mononuclear cell adhesion to platelet storage bag plastic polymers: a pilot study [J].
ElKattan, I ;
Anderson, J ;
Yun, JK ;
Colton, E ;
Yomtovian, R .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 1999, 6 (04) :509-513