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Abstrakty
A quantitative reversed-phase HPLC method has been developed that enables determination of both low endogenous and high therapeutic concentrations of N-acetylcysteine (NAC) in plasma. The compound is detected fluorimetrically after derivatisation with ortho-phthalaldehyde in the presence of a primary amine. Validation of the method revealed injection and method repeata-bility were good. The linear range was adequate and the limit of quantifi-cation was between 0.4 and 0.6 žM. Recovery of N-acetylcysteine from plasma samples was also acceptable. This method was applied to plasma samples from patients with a clinical septic shock who had received very high doses of N-acetylcys-teine. Six samples were taken at different times after administration of N-acetylcysteine. The blood-concentration profiles obtained indicate the me-thod is suitable for following the evolution of NAC in plasma under these conditions and can therefore be used for pharmacokinetic profiling.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Strony
149--164
Opis fizyczny
Bibliogr. 23 poz., rys., tab.
Twórcy
autor
- Dept. of Pharmaceutical and Biomedical Analysis, Pharmaceutical Institute, Vrije Universiteit Brussel-VUB, Laarbeeklaan 103, B-1090 Brussels, Belgium
autor
- Dept. of Pharmaceutical and Biomedical Analysis, Pharmaceutical Institute, Vrije Universiteit Brussel-VUB, Laarbeeklaan 103, B-1090 Brussels, Belgium
autor
- Dept. of Pharmaceutical and Biomedical Analysis, Pharmaceutical Institute, Vrije Universiteit Brussel-VUB, Laarbeeklaan 103, B-1090 Brussels, Belgium
autor
- Dept. of Intensive Care, Academic Hospital, Vrije Universiteit Brussel, Brussels, Belgium
Bibliografia
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- [2] L.E. Schmidt, T.T. Knudsen, K. Dalhoff, and F. Bendtsen, Lancet, 360,1151 (2002)
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- [5] H.D. Spapen, D.N. Nguyen, K. ver Elst, Y. Vander Heyden, and L.P. Huyghens, Clin. Intensive Care, 13, 27 (2002)
- [6] H.F. Galley, P.D. Howdle, B.E. Walker, and N.R. Webster, Free Radical Biol. Med., 23, 768 (1997)
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- [16] A.I. Al-Amoud, B.J. Clark, and H. Chrystyn, J. Chromatogr. B, 769, 89 (2002)
- [17] C. Vannecke, S. Baré, M. Bloomfield, D.L. Massart, J. Pharm. Biomed. Anal., 18, 963 (1999)
- [18] C. Vannecke, E. Van Gyseghem, M.S. Bloomfield, T. Coomber, Y. Vander Heyden, and D.L. Massart, Anal. Chim. Acta, 446, 413 (2001)
- [19] C. Vannecke, M.S. Bloomfield, Y. Vander Heyden, and D.L. Massart, Anal. Chim. Acta, 455, 117 (2002)
- [20] P.A. Lewis, A.J. Woodward, and J. Maddock, J. Chromatogr., 327, 261 (1985)
- [21] D.L. Massart, B.G.M. Vandeginste, L.M.C. Buydens, S. De Jong, P.J. Lewi, and J. Smeyers-Verbeke, Handbook of Chemometrics and Qualimetrics: Part A, Elsevier, Amsterdam, 1997, p. 187
- [22] E. Chapuzet, N. Mercier, S. Bervoas-Martin, B. Boulanger, P. Chevalier, P. Chiap, D. Grandjean, P. Hubert, P. Lagorce, M. Lallier, M.C. Lapparra, M. Laurentie, and J.C. Nivet, S.T.P. Pharma Pratiques, 7, 169 (1997)
- [23] H. Spapen, Y. Vander Heyden, M. Diltoer, J. Ramet, L. Massart, and L. Huyghens, Am. J. Resp. Crit. Care, 157, A296 (1998)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BAT3-0028-0059