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

Citation
B. Hafemann et al., Cross-linking by 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) of acollagen/elastin membrane meant to be used as a dermal substitute: effectson physical, biochemical and biological features in vitro, J MAT S-M M, 12(5), 2001, pp. 437-446
Citations number
37
Categorie Soggetti
Multidisciplinary
Journal title
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE
ISSN journal
09574530 → ACNP
Volume
12
Issue
5
Year of publication
2001
Pages
437 - 446
Database
ISI
SICI code
0957-4530(2001)12:5<437:CB1(OA>2.0.ZU;2-2
Abstract
Next to in vitro-cultured autogeneic keratinocytes for the restoration of e pidermis, a suitable dermal matrix is a mandatory component of an artificia l skin substitute for the permanent covering of full thickness skin defects . In our model a xenogeneic membrane, consisting of processed native collag en and elastin of porcine origin is meant to serve as a template for the fo rmation of a neo-dermis. In order to improve the resistance of this matrix against enzymatical degradation, we cross-linked it by using the carbodiimi de 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) together with N-hyd roxysuccinimide. Chemical cross-linking by these agents at two different de grees (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 t his membrane, we did not observe a difference between cross-linked and non- cross-linked material (shrinkage temperature 48 degreesC). We therefore exp ect that cross-linking by EDC is an effective means to control the degradat ion of the collagen/elastin membranes in vivo without a significant influen ce on their biocompatibility. (C) 2001 Kluwer Academic Publishers.