Determination of hydrazine in biofluids by capillary gas chromatography with nitrogen-sensitive or mass spectrometric detection
Determination of hydrazine in biofluids by capillary gas chromatography with nitrogen-sensitive or mass spectrometric detection
Plasma and liver levels of hydrazine were determined at 10, 30, 90 and 270 min in rats given 0.09, 0.27, 0.84 and 2.53 mmol of hydrazine per kg body weight orally by capillary gas chromatography-mass spectrometry of its pentafluorobenzaldehyde adduct (DFBA, m/z 388) using selected ion monitoring with 15N2-labelled hydrazine as the internal standard (adduct, m/z 390). The mean half-life for hydrazine in the plasma was approximately 2 h but varied with dose. Urinary excretion (0-24 h) of hydrazine and its metabolite acetylhydrazine were determined employing nitrogen-phosphorus detection of the adducts utilising a novel internal standard, pentafluorophenylhydrazine, the adduct of which structurally resembles DFBA. The fraction of the original dose excreted as hydrazine (and acetylhydrazine) declined with increasing dose.
227-234
Preece, N.E.
15e27a97-2717-4a2a-9e7e-4e31aefb21fb
Forrow, S.
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Ghatineh, S.
7b9ecea5-cdec-4c5d-9292-290dc0773404
Langley, G.J.
7ac80d61-b91d-4261-ad17-255f94ea21ea
Timbrell, J.A.
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17 January 1992
Preece, N.E.
15e27a97-2717-4a2a-9e7e-4e31aefb21fb
Forrow, S.
f579f77f-f2a1-4270-a059-d021990b96f2
Ghatineh, S.
7b9ecea5-cdec-4c5d-9292-290dc0773404
Langley, G.J.
7ac80d61-b91d-4261-ad17-255f94ea21ea
Timbrell, J.A.
dd1fd50f-1788-4edf-b89b-02f0aead91ab
Preece, N.E., Forrow, S., Ghatineh, S., Langley, G.J. and Timbrell, J.A.
(1992)
Determination of hydrazine in biofluids by capillary gas chromatography with nitrogen-sensitive or mass spectrometric detection.
Journal of Chromatography B: Biomedical Sciences and Applications, 573 (2), .
(doi:10.1016/0378-4347(92)80123-8).
Abstract
Plasma and liver levels of hydrazine were determined at 10, 30, 90 and 270 min in rats given 0.09, 0.27, 0.84 and 2.53 mmol of hydrazine per kg body weight orally by capillary gas chromatography-mass spectrometry of its pentafluorobenzaldehyde adduct (DFBA, m/z 388) using selected ion monitoring with 15N2-labelled hydrazine as the internal standard (adduct, m/z 390). The mean half-life for hydrazine in the plasma was approximately 2 h but varied with dose. Urinary excretion (0-24 h) of hydrazine and its metabolite acetylhydrazine were determined employing nitrogen-phosphorus detection of the adducts utilising a novel internal standard, pentafluorophenylhydrazine, the adduct of which structurally resembles DFBA. The fraction of the original dose excreted as hydrazine (and acetylhydrazine) declined with increasing dose.
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Published date: 17 January 1992
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Local EPrints ID: 498573
URI: http://eprints.soton.ac.uk/id/eprint/498573
ISSN: 0378-4347
PURE UUID: e7083e69-4275-4023-a083-19b8201de37d
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Date deposited: 21 Feb 2025 17:34
Last modified: 22 Feb 2025 02:34
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Author:
N.E. Preece
Author:
S. Forrow
Author:
S. Ghatineh
Author:
J.A. Timbrell
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