Hybrid optimal descriptors as a tool to predict skin sensitization in accordance to OECD principles

被引:42
作者
Toropova, Alla P. [1 ]
Toropov, Andrey A. [1 ]
机构
[1] Ist Ric Farmacol Mario Negri, IRCCS, Via La Masa 19, I-20156 Milan, Italy
关键词
SMILES; Skin sensitization; OECD principles; QSAR; Monte Carlo method; CORAL software; MONTE-CARLO METHOD; QSAR MODELS; TESTING STRATEGY; QSPR PREDICTION; RETENTION TIMES; SMILES; NANOPARTICLES; TOXICITY; DECONTAMINATION; INHIBITORS;
D O I
10.1016/j.toxlet.2017.03.023
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Skin sensitization (allergic contact dermatitis) is a widespread problem arising from the contact of chemicals with the skin. The detection of molecular features with undesired effect for skin is complex task owing to unclear biochemical mechanisms and unclearness of conditions of action of chemicals to skin. The development of computational methods for estimation of this endpoint in order to reduce animal testing is recommended (Cosmetics Directive EC regulation 1907/2006; EU Regulation, Regulation, 1223/2009). The CORAL software (http://www.insilico.eu/coral) gives good predictive models for the skin sensitization. Simplified molecular input-line entry system (SMILES) together with molecular graph are used to represent the molecular structure for these models. So-called hybrid optimal descriptors are used to establish quantitative structure-activity relationships (QSARs). The aim of this study is the estimation of the predictive potential of the hybrid descriptors. Three different distributions into the training (approximate to 70%), calibration (approximate to 45%), and validation (approximate to 15%) sets are studied. QSAR for these three distributions are built up with using the Monte Carlo technique. The statistical characteristics of these models for external validation set are used as a measure of predictive potential of these models. The best model, according to the above criterion, is characterized by n(vahdation) = 29, r(vaudation)(2) = 0.8596, RMSEvandation = 0.489. Mechanistic interpretation and domain of applicability for these models are defined.
引用
收藏
页码:57 / 66
页数:10
相关论文
共 62 条
[11]  
Cronin M T, 1994, SAR QSAR Environ Res, V2, P159, DOI 10.1080/10629369408029901
[12]   On spectral radius and energy of extended adjacency matrix of graphs [J].
Das, Kinkar Ch. ;
Gutman, Ivan ;
Furtula, Boris .
APPLIED MATHEMATICS AND COMPUTATION, 2017, 296 :116-123
[13]   Mechanism-Based QSAR Modeling of Skin Sensitization [J].
Dearden, J. C. ;
Hewitt, M. ;
Roberts, D. W. ;
Enoch, S. J. ;
Rowe, P. H. ;
Przybylak, K. R. ;
Vaughan-Williams, G. D. ;
Smith, M. L. ;
Pillai, G. G. ;
Katritzky, A. R. .
CHEMICAL RESEARCH IN TOXICOLOGY, 2015, 28 (10) :1975-1986
[14]   Skin sensitization: Modeling based on skin metabolism simulation and formation of protein conjugates [J].
Dimitrov, SD ;
Low, LK ;
Patlewicz, GY ;
Kern, PS ;
Dimitrova, GD ;
Comber, MHI ;
Phillips, RD ;
Niemela, J ;
Bailey, PT ;
Mekenyan, OG .
INTERNATIONAL JOURNAL OF TOXICOLOGY, 2005, 24 (04) :189-204
[15]   QSAR Study for Carcinogenicity in a Large Set of Organic Compounds [J].
Duchowicz, Pablo R. ;
Comelli, Nieves C. ;
Ortiz, Erlinda V. ;
Castro, Eduardo A. .
CURRENT DRUG SAFETY, 2012, 7 (04) :282-288
[16]   Relation between second and third geometric-arithmetic indices of trees [J].
Furtula, Boris ;
Gutman, Ivan .
JOURNAL OF CHEMOMETRICS, 2011, 25 (02) :87-91
[17]   Predicting the cytotoxicity of ionic liquids using QSAR model based on SMILES optimal descriptors [J].
Ghaedi, Abdolmohammad .
JOURNAL OF MOLECULAR LIQUIDS, 2015, 208 :269-279
[18]   Monte Carlo method for predicting of cardiac toxicity: hERG blocker compounds [J].
Gobbi, Marco ;
Beeg, Marten ;
Toropova, Mariya A. ;
Toropov, Andrey A. ;
Salmona, Mario .
TOXICOLOGY LETTERS, 2016, 250 :42-46
[19]   Quantitative structure-property relationship modeling of skin sensitization: A quantitative prediction [J].
Golla, Sharath ;
Madihally, Sundar ;
Robinson, Robert L., Jr. ;
Gasem, Khaled A. M. .
TOXICOLOGY IN VITRO, 2009, 23 (03) :454-465
[20]  
Grace P, 2003, QSAR COMB SCI, V22, P196