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Probing the Primary Mechanisms Affecting the Environmental Distribution of Estrogen and Androgen Isomers

Release Time:2019-03-09  Hits:

Indexed by: Journal Article

Date of Publication: 2011-05-01

Journal: ENVIRONMENTAL SCIENCE & TECHNOLOGY

Included Journals: ISTIC、PKU、PubMed、EI、SCIE、Scopus

Volume: 45

Issue: 9

Page Number: 3989-3995

ISSN: 0013-936X

Abstract: Land application of animal manure has been identified as a source of natural and synthetic hormone contaminants that are frequently detected down-gradient of agricultural operations. Much research on the environmental fate of hormones has focused on the structural isomers most biologically active in mammals, e.g., the 17 beta-isomers of the estrogen estradiol (E2) and the synthetic androgen trenbolone (TB). However, recent work has shown that the alpha- and beta-isomers of E2 and TB can cause comparable effects on certain aquatic species. To improve our understanding and ability to predict isomer-specific interactions with environmental sorbents, we measured the association (K(DOC)) of the alpha- and beta-isomers of E2 and TB as well as their primary metabolites (estrone and trendione) with two commercial dissolved organic carbon (DOC) sources by measuring both free and DOC-bound hormone concentrations. We also measured solvent-water partition coefficients partitioning (K(SW)) for the same hormones using hexane, toluene, and octanol. Log K(DOC) log.K(OC) (OC-normalized sorption by soils), and K(OW) values are all greater for the beta-isomer except between the E2 isomers. Theoretical descriptors reflecting electronic character and solute-solvent interactions were calculated to elucidate isomer-specific behavior. Trends for log K(OW) and log K(DOC) among hormones as well as between isomers are explained reasonably well by computed electrostatic potential and H-bonding parameters.

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