Cross-linking by 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) of a collagen/elastin membrane meant to be used as a dermal substitute:: effects on physical, biochemical and biological features in vitro

被引:58
作者
Hafemann, B [1 ]
Ghofrani, K
Gattner, HG
Stieve, H
Pallua, N
机构
[1] Univ Technol, Clin Plast Surg Hand & Burn Surg, D-52057 Aachen, Germany
[2] Univ Technol, Interdisciplinary Ctr Clin Res Biomat, D-52057 Aachen, Germany
[3] Univ Technol, Inst Text & Macromol Chem, D-52057 Aachen, Germany
[4] Univ Technol, Inst Biol 2, D-52057 Aachen, Germany
关键词
D O I
10.1023/A:1011205221972
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
Next to in vitro-cultured autogeneic keratinocytes for the restoration of epidermis, a suitable dermal matrix is a mandatory component of an artificial skin substitute for the permanent covering of full thickness skin defects. In our model a xenogeneic membrane, consisting of processed native collagen and elastin of porcine origin is meant to serve as a template for the formation of a neo-dermis. In order to improve the resistance of this matrix against enzymatical degradation, we cross-linked it by using the carbodiimide 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) together with N-hydroxysuccinimide. Chemical cross-linking by these agents at two different degrees (shrinkage temperatures 63 degreesC and 81 degreesC) had no relevant effect on mechanical features or water-uptake capacity. The time needed for enzymatic digestion was increased by cross-linking. Concerning growth and spreading of fibroblasts and keratinocytes on and within the structure of this membrane, we did not observe a difference between cross-linked and non-cross-linked material (shrinkage temperature 48 degreesC). We therefore expect that cross-linking by EDC is an effective means to control the degradation of the collagen/elastin membranes in vivo without a significant influence on their biocompatibility. (C) 2001 Kluwer Academic Publishers.
引用
收藏
页码:437 / 446
页数:10
相关论文
共 38 条
[1]
ARONS JA, 1992, SURGERY, V111, P4
[2]
LIVING TISSUE FORMED INVITRO AND ACCEPTED AS SKIN-EQUIVALENT TISSUE OF FULL THICKNESS [J].
BELL, E ;
EHRLICH, HP ;
BUTTLE, DJ ;
NAKATSUJI, T .
SCIENCE, 1981, 211 (4486) :1052-1054
[3]
TRANSPLANTATION STUDIES ON SHEETS OF PURE EPIDERMAL EPITHELIUM AND ON EPIDERMAL CELL SUSPENSIONS [J].
BILLINGHAM, RE ;
REYNOLDS, J .
BRITISH JOURNAL OF PLASTIC SURGERY, 1952, 5 (01) :25-36
[4]
BOYCE ST, 1988, SURGERY, V103, P421
[5]
SKIN-GRAFTING - DERMAL COMPONENTS IN INHIBITION OF WOUND CONTRACTION [J].
BROWN, D ;
GARNER, W ;
YOUNG, VL .
SOUTHERN MEDICAL JOURNAL, 1990, 83 (07) :789-795
[6]
In vitro degradation of dermal sheep collagen cross-linked using a water-soluble carbodiimide [J].
Damink, LHHO ;
Dijkstra, PJ ;
vanLuyn, MJA ;
vanWachem, PB ;
Nieuwenhuis, P ;
Feijen, J .
BIOMATERIALS, 1996, 17 (07) :679-684
[7]
DESAI M H, 1991, Journal of Burn Care and Rehabilitation, V12, P540, DOI 10.1097/00004630-199111000-00009
[8]
DIVINCENTI FC, 1969, PLAST RECONSTR SURG, V44, P464
[9]
GOSPODAROWICZ D, 1979, COLD SPRING HARBOR C, P561
[10]
GROWTH OF CULTURED HUMAN EPIDERMAL-CELLS INTO MULTIPLE EPITHELIA SUITABLE FOR GRAFTING [J].
GREEN, H ;
KEHINDE, O ;
THOMAS, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (11) :5665-5668