Evaluation of the capacity of the SCGE assay to assess the genotoxicity of biomaterials

被引:28
作者
Chauvel-Lebret, DJ
Auroy, P
Tricot-Doleux, S
Bonnaure-Mallet, M
机构
[1] Univ Rennes 1, UPRES EA 1256, Equipe Biol Buccale, F-35000 Rennes, France
[2] Univ Rennes 1, Fac Med, Lab Biomat Site Osseux, F-35043 Rennes, France
基金
澳大利亚研究理事会;
关键词
biocompatible materials; genotoxicity; elastomers; comet test; SCGE assay; cell culture;
D O I
10.1016/S0142-9612(00)00351-3
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
The comet test or SCGE assay, which is already widely used in other areas, has never been used to evaluate the mutagenic potential of medical biomaterials in the final form. The purpose of our study was thus to assess the comet test as a means of assessing the genotoxic potential of finished medical biomaterials. We used silicone elastomers with increasing concentrations of 4-nitroquinoline oxide, a genotoxic agent. Hydrogen peroxide was used as the positive control, and tissue culture polystyrene as the negative control. In our study, the comet test did not detect a significant difference in genotoxicity between the pure elastomer and the same elastomer containing 0.01mg/ml 4-nitroquinoline oxide, but did detect a significant difference between two elastomers containing 0.01 and 0.3mg/ml of 4-nitroquinoline oxide, respectively Since, the surface properties of the samples were identical, only the chemical composition may have caused significant differences in mutagenicity. Whatever the cause of the genotoxicity detected by the SCGE assay, testing finished biomaterials using the comet assay makes it possible to evaluate interactions between biomaterials and living tissues that are much closer to actual application conditions. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1795 / 1801
页数:7
相关论文
共 46 条
[1]
In vitro genotoxic effects of hard metal particles assessed by alkaline single cell gel and elution assays [J].
Anard, D ;
KirschVolders, M ;
Elhajouji, A ;
Belpaeme, K ;
Lison, D .
CARCINOGENESIS, 1997, 18 (01) :177-184
[2]
The International Comet Assay Workshop [J].
Anderson, D ;
Plewa, MJ .
MUTAGENESIS, 1998, 13 (01) :67-73
[3]
Optimization and standardization of the "comet assay" for analyzing the repair of DNA damage in cells [J].
Bauch, T ;
Böcker, W ;
Mallek, U ;
Müller, WU ;
Streffer, C .
STRAHLENTHERAPIE UND ONKOLOGIE, 1999, 175 (07) :333-340
[4]
Bocker W, 1997, INT J RADIAT BIOL, V72, P449, DOI 10.1080/095530097143220
[5]
Breast implants and cancer [J].
Brinton, LA ;
Brown, SL .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (18) :1341-1349
[6]
GENOTOXIC EFFECTS OF ERIOFLORIN ACETATE AND ERIOFLORIN METHACRYLATE - SESQUITERPENE LACTONES ISOLATED FROM PODANTHUS-OVATIFOLIUS LAG (COMPOSITAE) [J].
CEA, G ;
ALARCON, M ;
WEIGERT, G ;
SEPULVEDA, R .
BULLETIN OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 1990, 44 (01) :19-28
[7]
Evaluation of the in vitro biocompatibility of various elastomers [J].
Chauvel-Lebret, DJ ;
Pellen-Mussi, P ;
Auroy, P ;
Bonnaure-Mallet, M .
BIOMATERIALS, 1999, 20 (03) :291-299
[8]
DIRECT ENZYMATIC DETECTION OF ENDOGENOUS OXIDATIVE BASE DAMAGE IN HUMAN LYMPHOCYTE DNA [J].
COLLINS, AR ;
DUTHIE, SJ ;
DOBSON, VL .
CARCINOGENESIS, 1993, 14 (09) :1733-1735
[9]
The comet assay: What can it really tell us? [J].
Collins, AR ;
Dobson, VL ;
Dusinska, M ;
Kennedy, G ;
Stetina, R .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1997, 375 (02) :183-193
[10]
THE KINETICS OF REPAIR OF OXIDATIVE DNA-DAMAGE (STRAND BREAKS AND OXIDIZED PYRIMIDINES) IN HUMAN-CELLS [J].
COLLINS, AR ;
MA, AG ;
DUTHIE, SJ .
MUTATION RESEARCH-DNA REPAIR, 1995, 336 (01) :69-77