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  4. A k-NN algorithm for predicting oral sub-chronic toxicity in the rat
 
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2014
Journal Article
Title

A k-NN algorithm for predicting oral sub-chronic toxicity in the rat

Title Supplement
[with supplementary data]
Abstract
Repeated dose toxicity is of the utmost importance to characterize the toxicological profile of a chemical after repeated administration. Its evaluation refers to the Lowest-Observed-(Adverse)-Effect-Level (LO(A)EL) explicitly requested in several regulatory contexts, such as REACH and EC Regulation 1223/2009 on cosmetic products. So far in vivo tests have been the sole viable option to assess repeated dose toxicity. We report a customized k-nearest neighbors (k-NN) approach for predicting sub-chronic oral toxicity in rats. A training set of 254 chemicals was used to derive models whose robustness was challenged through leave-one-out cross-validation. Their predictive power was evaluated on an external dataset comprising 179 chemicals. Despite the intrinsically heterogeneous nature of the data, our models give promising results, with q2 >= 0.632 and external r2 >= 0.543. The confidence in prediction was ensured by implementing restrictive user-adjustable rules, excluding suspicious chemicals irrespective of the goodness in their prediction. Comparison with the very few LO(A)EL predictive models in the literature indicates that the results of the present analysis can be valuable in prioritizing the safety assessment of chemicals and thus making safe decisions and justifying waiving animal tests according to current regulations concerning chemical safety.
Author(s)
Gadaleta, Domenico
Pizzo, Fabiola
Lombardo, Anna
Carotti, Angelo
Escher, Sylvia E.
Nicolotti, Orazio
Benfenati, Emilio
Journal
Alternatives to animal experimentation : ALTEX  
Open Access
DOI
10.14573/altex.1405091
Additional link
Full text
Language
English
Fraunhofer-Institut für Toxikologie und Experimentelle Medizin ITEM  
Keyword(s)
  • k-nearest neighbor

  • repeated dose toxicity

  • lowest observed (adverse) effect level

  • REACH

  • QSAR

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