Structure-activity models for contact sensitization

被引:35
作者
Fedorowicz, A [1 ]
Singh, H
Soderholm, S
Demchuk, E
机构
[1] NIOSH, Morgantown, WV 26505 USA
[2] W Virginia Univ, Dept Stat, Morgantown, WV 26506 USA
[3] W Virginia Univ, Sch Pharm, Morgantown, WV 26506 USA
关键词
D O I
10.1021/tx0497806
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Allergic contact dermatitis (ACD) is a widespread cause of workers' disabilities. Although some substances found in the workplace are rigorously tested, the potential of the vast majority of chemicals to cause skin sensitization remains unknown. At the same time, exhaustive testing of all chemicals in workplaces is costly and raises ethical concerns. New approaches to developing information for risk assessment based on computational (quantitative) structure-activity relationship [(Q)SAR] methods may be complementary to and reduce the need for animal testing. Virtually any number of existing, de novo, and even preconceived compounds can be screened in silico at a fraction of the cost of animal testing. This work investigates the utility of ACD (Q)SAR modeling from the occupational health perspective using two leading software products, DEREK for Windows and TOPKAT, and an original method based on logistic regression methodology. It is found that the correct classification of (Q)SAR predictions for guinea pig data achieves values of 73.3, 82.9, and 87.6% for TOPKAT, DEREK for Windows, and the logistic regression model, respectively. The correct classification using LLNA data equals 73.0 and 83.2% for DEREK for Windows and the logistic regression model, respectively.
引用
收藏
页码:954 / 969
页数:16
相关论文
共 67 条
[41]  
2-I
[42]   A CLASSIFICATION MODEL FOR ALLERGIC CONTACT-DERMATITIS [J].
MAGEE, PS ;
HOSTYNEK, JJ ;
MAIBACH, HI .
QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS, 1994, 13 (01) :22-33
[43]   Predicting the genotoxicity of secondary and aromatic amines using data subsetting to generate a model ensemble [J].
Mattioni, BE ;
Kauffman, GW ;
Jurs, PC ;
Custer, LL ;
Durham, SK ;
Pearl, GM .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 2003, 43 (03) :949-963
[44]  
MORIGUCHI I, 1992, CHEM PHARM BULL, V40, P127
[45]   Predicting the genotoxicity of thiophene derivatives from molecular structure [J].
Mosier, PD ;
Jurs, PC ;
Custer, LL ;
Durham, SK ;
Pearl, GM .
CHEMICAL RESEARCH IN TOXICOLOGY, 2003, 16 (06) :721-732
[46]  
Myers R., 1990, CLASSICAL MODERN REG
[47]  
National Institute on Drug Abuse, 1999, NIH PUBL, V09-4180
[48]   Fuzzy modeling of skin permeability coefficients [J].
Pannier, AK ;
Brand, RM ;
Jones, DD .
PHARMACEUTICAL RESEARCH, 2003, 20 (02) :143-148
[49]   Skin-sensitization structure-activity relationships for aldehydes [J].
Patlewicz, G ;
Basketter, DA ;
Smith, CK ;
Hotchkiss, SAM ;
Roberts, DW .
CONTACT DERMATITIS, 2001, 44 (06) :331-336
[50]   Metric validation and the receptor-relevant subspace concept [J].
Pearlman, RS ;
Smith, KM .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1999, 39 (01) :28-35