CYTOTOXICITY TESTING OF WOUND DRESSINGS USING NORMAL HUMAN KERATINOCYTES IN CULTURE

被引:48
作者
ROSDY, M
CLAUSS, LC
机构
[1] QA department, Dow Corning European Health Care France, Valbonne, 06561, S.A. Route des cretes-B.P. 43, Sophia Antipolis-Les Bouillides
来源
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH | 1990年 / 24卷 / 03期
关键词
D O I
10.1002/jbm.820240308
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Comparative cytotoxicity testing of 16 wound dressings of different composition show that normal human keratinocytes (NHK) growing on a fibroblastic feeder layer are as sensitive to toxic materials by direct contact as the confluent MRC5 fibroblasts used for standard cell culture cytotoxicity testing, and slightly more sensitive when extracts of the dressings were tested. After direct contact with each of the cell types, we found effects due to 12 dressing samples (75%), but the extracts of only 6 of them induced changes in cell shape or cell death on NHK, and 4 of them on MRC5 cells. In order to assess the compatibility of these dressings with a pure population of epidermal cells, the cell type responsible for reepidermization of healing wounds, we then tested the sensitivity, both to dressing samples and extracts, of normal human keratinocytes (NHK) grown in chemically defined medium and without a feeder layer: The results show epidermal cytocompatibility of 10 dressing extracts, while 6 others induced cytopathic effects. Three of these extracts specifically damaged epidermal cells and inhibited their proliferation. When comparing the sensitivities of NHK (in defined medium) and MRC5 cells, we observed complete correlation for 75% of the dressings by extract testing and in 94% of the cases after direct contact. Copyright © 1990 John Wiley & Sons, Inc.
引用
收藏
页码:363 / 377
页数:15
相关论文
共 30 条
[1]   CELL-MIGRATION IS ESSENTIAL FOR SUSTAINED GROWTH OF KERATINOCYTE COLONIES - THE ROLES OF TRANSFORMING GROWTH FACTOR-ALPHA AND EPIDERMAL GROWTH-FACTOR [J].
BARRANDON, Y ;
GREEN, H .
CELL, 1987, 50 (07) :1131-1137
[2]   CALCIUM-REGULATED DIFFERENTIATION OF NORMAL HUMAN EPIDERMAL-KERATINOCYTES IN CHEMICALLY DEFINED CLONAL CULTURE AND SERUM-FREE SERIAL CULTURE [J].
BOYCE, ST ;
HAM, RG .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1983, 81 (01) :S33-S40
[3]  
BOYCE ST, 1983, IN VITRO MODELS CANC
[4]  
BROWN GL, 1986, J EXP MED, V163, P1319
[5]   PRODUCTION AND AUTOINDUCTION OF TRANSFORMING GROWTH FACTOR-ALPHA IN HUMAN KERATINOCYTES [J].
COFFEY, RJ ;
DERYNCK, R ;
WILCOX, JN ;
BRINGMAN, TS ;
GOUSTIN, AS ;
MOSES, HL ;
PITTELKOW, MR .
NATURE, 1987, 328 (6133) :817-820
[6]  
DAVIES JE, 1987, 1986 P EUR C BIOM BO
[7]   KERATINOCYTE MIGRATION AND THE EXTRACELLULAR-MATRIX [J].
DONALDSON, DJ ;
MAHAN, JT .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1988, 90 (05) :623-628
[8]   SERUM-FREE SERIAL CULTURE OF ADULT HUMAN KERATINOCYTES FROM SUCTION-BLISTER ROOF EPIDERMIS [J].
FURUKAWA, F ;
HUFF, JC ;
WESTON, WL ;
NORRIS, DA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1987, 89 (05) :460-463
[9]  
FYRAND O, 1985, ACTA DERM-VENEREOL, V65, P379
[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