Predicting the cytotoxicity of disinfection by-products to Chinese hamster ovary by using linear quantitative structure-activity relationship models

被引:11
|
作者
Qin, Li-Tang [1 ,2 ,3 ]
Zhang, Xin [1 ]
Chen, Yu-Han [1 ]
Mo, Ling-Yun [1 ,2 ,3 ]
Zeng, Hong-Hu [1 ,2 ,3 ]
Liang, Yan-Peng [1 ,2 ,3 ]
Lin, Hua [1 ,2 ,3 ]
Wang, Dun-Qiu [1 ,2 ,3 ]
机构
[1] Guilin Univ Technol, Coll Environm Sci & Engn, Guilin 541004, Peoples R China
[2] Guilin Univ Technol, Guangxi Key Lab Environm Pollut Control Theory &, Guilin 541004, Peoples R China
[3] Guilin Univ Technol, Collaborat Innovat Ctr Water Pollut Control & Wat, Guilin 541004, Peoples R China
基金
中国国家自然科学基金;
关键词
Disinfection by-products; Quantitative structure-activity relationship; Cytotoxicity; Chinese hamster ovary; MAMMALIAN-CELL CYTOTOXICITY; DRINKING-WATER; QSAR MODELS; EXTERNAL VALIDATION; HALOACETIC ACIDS; TOXICITY; GENOTOXICITY; QSPR; DBPS; SET;
D O I
10.1007/s11356-019-04947-z
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A suitable model to predict the toxicity of current and continuously emerging disinfection by-products (DBPs) is needed. This study aims to establish a reliable model for predicting the cytotoxicity of DBPs to Chinese hamster ovary (CHO) cells. We collected the CHO cytotoxicity data of 74 DBPs as the endpoint to build linear quantitative structure-activity relationship (QSAR) models. The linear models were developed by using multiple linear regression (MLR). The MLR models showed high performance in both internal (leave-one-out cross-validation, leave-many-out cross-validation, and bootstrapping) and external validation, indicating their satisfactory goodness of fit (R-2=0.763-0.799), robustness (Q(LOO)(2)=0.718-0.745), and predictive ability (CCC=0.806-0.848). The generated QSAR models showed comparable quality on both the training and validation levels. Williams plot verified that the obtained models had wide application domains and covered the 74 structurally diverse DBPs. The molecular descriptors used in the models provided comparable information that influences the CHO cytotoxicity of DBPs. In conclusion, the linear QSAR models can be used to predict the CHO cytotoxicity of DBPs.
引用
收藏
页码:16606 / 16615
页数:10
相关论文
共 50 条
  • [41] A review of quantitative structure-activity relationship: The development and current status of data sets, molecular descriptors and mathematical models
    Li, Jianmin
    Zhao, Tian
    Yang, Qin
    Du, Shijie
    Xu, Lu
    CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 2025, 256
  • [42] MONTE CARLO-BASED QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP MODELS FOR TOXICITY OF ORGANIC CHEMICALS TO DAPHNIA MAGNA
    Toropova, Alla P.
    Toropov, Andrey A.
    Veselinovic, Aleksandar M.
    Veselinovic, Jovana B.
    Leszczynska, Danuta
    Leszczynski, Jerzy
    ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 2016, 35 (11) : 2691 - 2697
  • [43] Exploring quantitative structure-activity relationship studies of antioxidant phenolic compounds obtained from traditional Chinese medicinal plants
    Mitra, Indrani
    Saha, Achintya
    Roy, Kunal
    MOLECULAR SIMULATION, 2010, 36 (13) : 1067 - 1079
  • [44] Predicting the Toxicity of Ionic Liquids in Leukemia Rat Cell Line by the Quantitative Structure-Activity Relationship Method Using Topological Indexes
    Yan, Fangyou
    Xia, Shuqian
    Wang, Qiang
    Ma, Peisheng
    INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2012, 51 (43) : 13897 - 13901
  • [45] Quantitative Structure-activity Relationship Analysis for Predicting Lipophilicity of Aniline Derivatives (Including Some Pharmaceutical Compounds)
    Rezaei, Morteza
    Mohammadinasab, Esmat
    Esfahani, Tahere Momeni
    COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2019, 22 (05) : 333 - 345
  • [46] QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP (QSAR) STUDIES IN GENETIC TOXICOLOGY - MATHEMATICAL-MODELS AND THE BIOLOGICAL-ACTIVITY TERM OF THE RELATIONSHIP
    BENIGNI, R
    GIULIANI, A
    MUTATION RESEARCH, 1994, 306 (02): : 181 - 186
  • [47] Estimation of cytotoxicity to HEP-G2 cells of 255 environmental pollutants and water using QSAR (Quantitative Structure-Activity Relationship)
    Shoji, R
    Miyazaki, T
    Nishimiya, T
    JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART A-TOXIC/HAZARDOUS SUBSTANCES & ENVIRONMENTAL ENGINEERING, 2003, 38 (12): : 2807 - 2823
  • [48] Interpretable, Probability-Based Confidence Metric for Continuous Quantitative Structure-Activity Relationship Models
    Keefer, Christopher E.
    Kauffman, Gregory W.
    Gupta, Rishi Raj
    JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2013, 53 (02) : 368 - 383
  • [49] Quantitative Structure-activity Relationship for Heterogeneous Phenol Compounds Using Zero Point Energy
    Jin Biao
    Liu Cui
    Jin Qiao
    CHINESE JOURNAL OF STRUCTURAL CHEMISTRY, 2010, 29 (09) : 1353 - 1361
  • [50] Quantitative structure-activity relationship studies of TIBO derivatives using support vector machines
    Darnag, R.
    Schmitzer, A.
    Belmiloud, Y.
    Villemin, D.
    Jarid, A.
    Chait, A.
    Mazouz, E.
    Cherqaoui, D.
    SAR AND QSAR IN ENVIRONMENTAL RESEARCH, 2010, 21 (3-4) : 231 - 246