EPA Science Inventory

Identification of Bound Nitro Musk-Protein Adduct in Fish Liver By Gas Chromatography-Mass Sectrometry: Biotransformation, Dose-Response and Toxicokinetics of Nitro Musk Metabolites Protein Adducts in Trout Liver as Biomarker of Exposure

Citation:

Mottaleb, A. M., L. I. OSEMWENGIE, R. M. Islam, AND G. SOVOCOOL. Identification of Bound Nitro Musk-Protein Adduct in Fish Liver By Gas Chromatography-Mass Sectrometry: Biotransformation, Dose-Response and Toxicokinetics of Nitro Musk Metabolites Protein Adducts in Trout Liver as Biomarker of Exposure. AQUATIC TOXICOLOGY. Elsevier Science Ltd, New York, NY, 106(107):164-172, (2012).

Description:

Ubiquitous occurrences of synthetic nitro musks are evident in the literature. The In vivo analysis of musk xylene (MX) and musk ketone (MK) - protein adducts in trout liver have been performed by gas chromatography-mass spectrometry using selected ion monitoring (GC-SIM-MS). Biotransformation, dose-response and toxicokinetics studies of 2-amino-MX (2-AMX), 2-amino-MK (2-AMK) and 4-amino-MX (4-AMX) metabolites, covalently bound to cysteine amino acids in proteins in fish liver, formed by enzymatic nitro-reduction of MX and MK, have been described. Trout were exposed to single exposures of 0.010, 0.030, 0.10, and 0.30 mg/g MX and/or MK. Forty-two fish liver samples were collected from exposed- and control- fish subsequent to exposure intervals of 1 day, 3 days, and 7 days and were composited as per exposure schedules and times. Alkaline hydrolysis released bound metabolites from exposed liver composites that were extracted into n-hexane and then concentrated and analyzed by GC-SIM-MS. The presence of the metabolites in liver extracts was confirmed based on agreement of similar mass spectral properties and retention times with standards. In the dose-response study, the maximum adduct formation was 492.0 ng/g for 2-AMX, 505.5 ng/g for 2-AMK and 12588.5 ng/g for 4-AMX in liver at 0.03 mg/g MX and MK fish in 1 day after exposure. For toxicokinetics investigation, the highest amount of the target metabolites was found to be the same concentration as observed in the dose-response study for 1 day after exposure with 0.03 mg/g MX and MK fish and the half-lives of the metabolites were estimated to be 2 to 9 days based on assumption of first-order kinetics. Average recoveries exceeded 95% with a relative standard deviation (RSD) around 9%, and the limit of detection (LOD) ranged from 0.91 to 3.8 ng/g based on a signal to noise ratio of 10 (S/N= 10) could be achieved for the metabolites. No metabolites were detected in the controls and exposed non-hydrolyzed liver extracts. This is the first report on dose-response and toxicokinetics of nitro musk-cysteine-protein adducts in fish liver.

Purpose/Objective:

Synthetic musk (SM) is often used in fragrances, soaps, lotions and other perfumed household personal care products as substitutes for the more expensive natural musk. Musk xylene (1,3-dimethyl-2,4,6-trinitro-5-tert-butylbenzene, MX) and musk ketone (1-tert-butyl-3,5-dimethyl-2,6-dinitro-4-acetylbenzene, MK) belong to the common group of nitro musk compounds with an estimated annual production of about 6,100 metric tons (Rimkus, 1999). The main environmental exposure of nitro musk occurs after sewage introduction and their ingredients enter into the environment and reach detectable and potential harmful concentration levels because most are not regulated environmental contaminants (Bethesda, 2006). The ubiquitous occurrence and fate of nitro musks and their metabolites as pollutants and biomarkers in the environment have led many scientists to research these emerging compounds (Daughton and Ternes, 1999, Kelly et al., 2007).

URLs/Downloads:

OSEMWENGIE 11-056 FINAL JOURNAL ARTICLE..PDF   (PDF,NA pp, 639 KB,  about PDF)

Record Details:

Record Type: DOCUMENT (JOURNAL/PEER REVIEWED JOURNAL)
Start Date: 06/12/2012
Completion Date: 06/12/2012
Record Last Revised: 07/02/2012
Record Created: 08/08/2011
Record Released: 08/08/2011
OMB Category: Other
Record ID: 237443

Organization:

U.S. ENVIRONMENTAL PROTECTION AGENCY

OFFICE OF RESEARCH AND DEVELOPMENT

NATIONAL EXPOSURE RESEARCH LAB

ENVIRONMENTAL SCIENCES DIVISION

ENVIRONMENTAL CHEMISTRY BRANCH