Functional modification of HHCB: Strategy for obtaining environmentally friendly derivatives

J Hazard Mater. 2021 Aug 15:416:126116. doi: 10.1016/j.jhazmat.2021.126116. Epub 2021 May 25.

Abstract

Galaxolide (HHCB), one of the most widely used synthetic musks in personal care products (PCPs), has been recognized as an emerging contaminant with potential human health concerns. To overcome such adverse effects, a systematic molecular design, screening and performance evaluation approach was developed to generate functionally improved and environmentally friendly HHCB derivatives. Among the 90 designed HHCB derivatives, 15 were screened with improved functional properties (i.e., odor stability and intensity) and less environmental impacts (i.e., lower bio-toxicity, bio-accumulation ability, and mobility) using 3D-QSAR models and density functional theory methods. Their human health risks were then assessed by toxicokinetic analysis, which narrowed the candidates to four. Derivative 7, the designed molecule with the least dermal adsorption potential, was evaluated for its interaction with other PCPs additives (i.e., anti-photosensitivity materials and moisturizer) and such impacts on human health risks using molecular docking and molecular dynamic simulation. The environmental fate of Derivative 7 after transformation (i.e., photodegradation, biotransformation, and chlorination) was also discussed. Biotransformation and chlorination were recognized as optimum options for Derivative 7 mitigation. This study provided the theoretical basis for the design of functionally improved and environmentally friendly HHCB alternatives and advanced the understanding of their environmental behaviors and health risks.

Keywords: 3D-QSAR models; Density function theory; Derivative modification; Molecular docking; Molecular dynamic simulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzopyrans
  • Biotransformation
  • Cosmetics*
  • Humans
  • Molecular Docking Simulation
  • Molecular Dynamics Simulation
  • Quantitative Structure-Activity Relationship*

Substances

  • Benzopyrans
  • Cosmetics