Pharmacokinetic profile of tert-butylaminoethanethiol

A preliminary study of the pharmacokinetic parameters of t-Butylaminoethanethiol (TBAESH) was performed after administration of a single dose (35 mg/kg) either orally or intravenously. Plasma or blood samples were treated with dithiothreitol, perchloric acid and, after filtration, submitted to furth...

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Main Authors: M. H. Guerra Andrade, A. C. T. Freire, D. L. Nelson
Format: Article
Language:English
Published: Fundação Oswaldo Cruz (FIOCRUZ) 1990-09-01
Series:Memorias do Instituto Oswaldo Cruz
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761990000300013
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author M. H. Guerra Andrade
A. C. T. Freire
D. L. Nelson
author_facet M. H. Guerra Andrade
A. C. T. Freire
D. L. Nelson
author_sort M. H. Guerra Andrade
collection DOAJ
description A preliminary study of the pharmacokinetic parameters of t-Butylaminoethanethiol (TBAESH) was performed after administration of a single dose (35 mg/kg) either orally or intravenously. Plasma or blood samples were treated with dithiothreitol, perchloric acid and, after filtration, submitted to further purification with anionic resin. In the final step the drug was retained on a cationic resin column, eluted with NaCl lM and detected according to the method of Ellman (1958). The results suggested a pharmacokinetic behavior related to a one open compartment model with the following values for the total drug: area under the intravenous curve (AUC i.v.): 443(+ ou -) 24.0; AUC oral: 85.5(+ ou -) 14.5 ug min.ml(elevado a -1); elimination rate constant: 0.069(+ ou -) 0.0055 min(elevado a -1), biological half-life: 10.0(+ ou -) 0.80 min; distribution volume 1.15(+ ou -) 0.15 ml/g; biodisponibility: 0.19(+ ou -) 0.02. From a pharmacokinetic standpoint, TBAESH seems to have no advantage over the analogous disulfide compound.
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spelling doaj.art-8d0af7425ea24281ae65af43eb5b99042023-08-02T09:28:26ZengFundação Oswaldo Cruz (FIOCRUZ)Memorias do Instituto Oswaldo Cruz0074-02761678-80601990-09-0185335335610.1590/S0074-02761990000300013Pharmacokinetic profile of tert-butylaminoethanethiolM. H. Guerra AndradeA. C. T. FreireD. L. NelsonA preliminary study of the pharmacokinetic parameters of t-Butylaminoethanethiol (TBAESH) was performed after administration of a single dose (35 mg/kg) either orally or intravenously. Plasma or blood samples were treated with dithiothreitol, perchloric acid and, after filtration, submitted to further purification with anionic resin. In the final step the drug was retained on a cationic resin column, eluted with NaCl lM and detected according to the method of Ellman (1958). The results suggested a pharmacokinetic behavior related to a one open compartment model with the following values for the total drug: area under the intravenous curve (AUC i.v.): 443(+ ou -) 24.0; AUC oral: 85.5(+ ou -) 14.5 ug min.ml(elevado a -1); elimination rate constant: 0.069(+ ou -) 0.0055 min(elevado a -1), biological half-life: 10.0(+ ou -) 0.80 min; distribution volume 1.15(+ ou -) 0.15 ml/g; biodisponibility: 0.19(+ ou -) 0.02. From a pharmacokinetic standpoint, TBAESH seems to have no advantage over the analogous disulfide compound.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761990000300013aminoethyl pharmacokinetics
spellingShingle M. H. Guerra Andrade
A. C. T. Freire
D. L. Nelson
Pharmacokinetic profile of tert-butylaminoethanethiol
Memorias do Instituto Oswaldo Cruz
aminoethyl pharmacokinetics
title Pharmacokinetic profile of tert-butylaminoethanethiol
title_full Pharmacokinetic profile of tert-butylaminoethanethiol
title_fullStr Pharmacokinetic profile of tert-butylaminoethanethiol
title_full_unstemmed Pharmacokinetic profile of tert-butylaminoethanethiol
title_short Pharmacokinetic profile of tert-butylaminoethanethiol
title_sort pharmacokinetic profile of tert butylaminoethanethiol
topic aminoethyl pharmacokinetics
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761990000300013
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