Toxicity and quantitative structure-activity relationships of benzoic acids to Pseudokirchneriella subcapitata

被引:64
|
作者
Lee, Po Yi [1 ]
Chen, Chung Yuan [1 ]
机构
[1] Natl Chiao Tung Univ, Inst Environm Engn, Hsinchu 300, Taiwan
关键词
Pseudokirchneriella subcapitata; Benzoic acids; NOEC; EC50; QSAR; ORGANIC TOXICANTS; GROWTH-INHIBITION; DAPHNIA-MAGNA; BACTERIA; NOECS;
D O I
10.1016/j.jhazmat.2008.09.086
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The present study presents the toxicity data of benzoic acid and its derivatives on Pseudokirchneriella subcapitata, in terms of EC50 and NOEC values. Median effective concentrations (EC50) range from 0.55 to 270.7 mg/L (based on final yield) and 1.93 to 726.3 mg/L (based on algal growth rate). No-observed-effect concentration (NOEC) is within the range of <0.0057-179.9 mg/L. From both the NOEC and EC50 values, it was found that, 2,4,6-trihydroxybenzoic acid, 4-chlorobenzoic acid, 3-bromobenzoic acid, 4-bromobenzoic acid, 2,6-dihydroxybenzoic acid. and 2,3,4-trihydroxybenzoic acid possess much higher risks to the aquatic organisms as compared to the other benzoic acids. These data are useful for risk assessment and protection of the aquatic environments, because such information is not available in the existing toxicological databases. The toxicity of halogenated benzoic acids was found to be directly related to the compound's hydrophobicity (the logarithm of the 1-octanol/water partition coefficient, logKow). On the other hand, the number of hydroxyl groups (N-OH) had a determinant influence to the toxicity of hydroxybenzoic acids. Quantitative structure-activity relationships were established to correlate the observed toxicity with logKow and N-OH values. These statistical correlations are highly significant with the predictive power Q ranging from 0.896 to 0.955. Furthermore, in terms of the species sensitivity, the luminescent bacteria (Microtox) and the alga P. subcapitata appeared to be more susceptible to benzoic acids than the water flea and ciliate. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:156 / 161
页数:6
相关论文
共 50 条
  • [21] In vitro toxicity of several dithiocarbamates and structure-activity relationships
    Segovia, N
    Crovetto, G
    Lardelli, P
    Espigares, M
    JOURNAL OF APPLIED TOXICOLOGY, 2002, 22 (06) : 353 - 357
  • [22] Quantitative structure-activity relationships (QSARs) using the novel marine algal toxicity data of phenols
    Erturk, M. Doga
    Sacan, Melek Turker
    Novic, Marjana
    Minovski, Nikola
    JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 2012, 38 : 90 - 100
  • [23] Quantitative structure-activity relationship models for bee toxicity
    Toropov, Andrey A.
    Toropova, Alla P.
    Como, Francesca
    Benfenati, Emilio
    TOXICOLOGICAL AND ENVIRONMENTAL CHEMISTRY, 2017, 99 (7-8) : 1117 - 1128
  • [24] Quantitative structure-activity relationships and the prediction of MHC supermotifs
    Doytchinova, IA
    Guan, PP
    Flower, DR
    METHODS, 2004, 34 (04) : 444 - 453
  • [25] Quantitative structure-activity relationships of sweet isovanillyl derivatives
    Bassoli, A
    Drew, MGB
    Hattotuwagama, CK
    Merlini, L
    Morini, G
    Wilden, GRW
    QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS, 2001, 20 (01): : 3 - 16
  • [26] Quantitative structure-activity relationships for organophosphates binding to acetylcholinesterase
    Ruark, Christopher D.
    Hack, C. Eric
    Robinson, Peter J.
    Anderson, Paul E.
    Gearhart, Jeffery M.
    ARCHIVES OF TOXICOLOGY, 2013, 87 (02) : 281 - 289
  • [27] Descriptor Selection Improvements for Quantitative Structure-Activity Relationships
    Xia, Liang-Yong
    Wang, Qing-Yong
    Cao, Zehong
    Liang, Yong
    INTERNATIONAL JOURNAL OF NEURAL SYSTEMS, 2019, 29 (09)
  • [28] Use of a (Quantitative) Structure-Activity Relationship [(Q)Sar] Model to Predict the Toxicity of Naphthenic Acids
    Frank, Richard A.
    Sanderson, Hans
    Kavanagh, Richard
    Burnison, B. Kent
    Headley, John V.
    Solomon, Keith R.
    JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, 2010, 73 (04): : 319 - 329
  • [29] Quantitative structure-activity relationships of α1 adrenergic antagonists
    Eric, S
    Solmajer, T
    Zupan, J
    Novic, M
    Oblak, M
    Agbaba, D
    JOURNAL OF MOLECULAR MODELING, 2004, 10 (02) : 139 - 150
  • [30] Quantitative structure-activity relationship between the toxicity of amine surfactant and its molecular structure
    Liu, Wengang
    Wang, Xinyang
    Zhou, Xiaotong
    Duan, Hao
    Zhao, Panxing
    Liu, Wenbao
    SCIENCE OF THE TOTAL ENVIRONMENT, 2020, 702