Quantitative structure-activity relationship modelling of oral acute toxicity and cytotoxic activity of fragrance materials in rodents

SAR QSAR Environ Res. 2009 Oct;20(7-8):767-79. doi: 10.1080/10629360903438669.

Abstract

Fragrance materials are used as ingredients in many consumer and personal care products. The wide and daily use of these substances, as well as their mainly uncontrolled discharge through domestic sewage, make fragrance materials both potential indoor and outdoor air pollutants which are also connected to possible toxic effects on humans (asthma, allergies, headaches). Unfortunately, little is known about the environmental fate and toxicity of these substances. However, the use of alternative, predictive approaches, such as quantitative structure-activity relationships (QSARs), can help in filling the data gap and in the characterization of the environmental and toxicological profile of these substances. In the proposed study, ordinary least squares regression-based QSAR models were developed for three toxicological endpoints: mouse oral LD(50), inhibition of NADH-oxidase (EC(50) NADH-Ox) and the effect on mitochondrial membrane potential (EC(50) DeltaPsim). Theoretical molecular descriptors were calculated by using DRAGON software, and the best QSAR models were developed according to the principles defined by the Organization for Economic Co-operation and Development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Cytotoxins / chemistry*
  • Cytotoxins / toxicity*
  • Inhibitory Concentration 50
  • Least-Squares Analysis
  • Lethal Dose 50
  • Membrane Potential, Mitochondrial / drug effects
  • Mice
  • Multienzyme Complexes / antagonists & inhibitors
  • NADH, NADPH Oxidoreductases / antagonists & inhibitors
  • Oils, Volatile / chemistry*
  • Oils, Volatile / toxicity*
  • Quantitative Structure-Activity Relationship

Substances

  • Cytotoxins
  • Multienzyme Complexes
  • Oils, Volatile
  • NADH oxidase
  • NADH, NADPH Oxidoreductases