Metabolism of the ethanolamine-type antihistamine diphenhydramine (Benadryl) TM by the fungus Cunninghamella elegans

Two strains of the filamentous fungus Cunninghamella elegans (ATCC 9245 and ATCC 36112) were grown in Sabouraud dextrose broth and screened for the ability to metabolize the ethanolamine-type antihistamine diphenhydramine. Based on the amount of parent drug recovered after 7days incubation, both C....

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Veröffentlicht in:Applied microbiology and biotechnology 2000-03, Vol.53 (3), p.310-315
Hauptverfasser: Moody, J. D., Heinze, T. M., Hansen Jr, E. B., Cerniglia, C. E.
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container_end_page 315
container_issue 3
container_start_page 310
container_title Applied microbiology and biotechnology
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creator Moody, J. D.
Heinze, T. M.
Hansen Jr, E. B.
Cerniglia, C. E.
description Two strains of the filamentous fungus Cunninghamella elegans (ATCC 9245 and ATCC 36112) were grown in Sabouraud dextrose broth and screened for the ability to metabolize the ethanolamine-type antihistamine diphenhydramine. Based on the amount of parent drug recovered after 7days incubation, both C. elegans strains metabolized approximately 74% of the diphenhydramine, 58% of this being identified as organic extractable metabolites. The organic extractable metabolites were isolated by reversed-phase high-performance liquid chromatography and identified by analyzing their mass and nuclear magnetic resonance spectra. Desorption chemical ionization mass spectrometry (DCIMS) with deuterated ammonia was used to differentiate possible isobaric diphenhydramine metabolites and to probe the mechanisms of ion formation under ammonia DCIMS conditions. C. elegans transformed diphenhydramine by demethylation, oxidation, and N-acetylation. The major metabolites observed were diphenhydramine-N-oxide (3%), N-desmethyldiphenhydramine (30%), N-acetyldidesmethyldiphenhydramine (13%), and N-acetyl-N-desmethyldiphenhydramine (12%). These compounds are known mammalian metabolites of diphenhydramine and may be useful for further toxicological studies.[PUBLICATION ABSTRACT]
doi_str_mv 10.1007/s002530050026
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Desorption chemical ionization mass spectrometry (DCIMS) with deuterated ammonia was used to differentiate possible isobaric diphenhydramine metabolites and to probe the mechanisms of ion formation under ammonia DCIMS conditions. C. elegans transformed diphenhydramine by demethylation, oxidation, and N-acetylation. The major metabolites observed were diphenhydramine-N-oxide (3%), N-desmethyldiphenhydramine (30%), N-acetyldidesmethyldiphenhydramine (13%), and N-acetyl-N-desmethyldiphenhydramine (12%). 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subjects Ammonia
Histamine
Ionization
Ions
Liquid chromatography
Mass spectrometry
Metabolism
Metabolites
Nematodes
NMR
Nuclear magnetic resonance
Worms
title Metabolism of the ethanolamine-type antihistamine diphenhydramine (Benadryl) TM by the fungus Cunninghamella elegans
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