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Influence of input rate on the stereospecific and nonstereospecific first pass metabolism and pharmacokinetics of metoprolol extended release formulations
Author(s) -
Mistry Bipin,
Leslie James L.,
Eddington Natalie D.
Publication year - 2002
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/chir.10045
Subject(s) - metoprolol , chemistry , pharmacokinetics , enantiomer , stereoselectivity , metabolite , high performance liquid chromatography , chromatography , absorption (acoustics) , pharmacology , stereochemistry , medicine , biochemistry , physics , acoustics , catalysis
The purpose of this study was to examine the influence of input rate on the stereoselective and nonstereoselective pharmacokinetics of metoprolol, α‐hydroxymetoprolol, and its acid metabolite. Extended release formulations (100 mg) of metoprolol with varying release rates (e.g., slow (S), moderate (M), and fast (F)) and an oral solution (OS, 50 mg) were administered to normal, healthy extensive metabolizers. Serial blood samples were collected over 48 h, plasma was obtained, and subsequently analyzed by a validated HPLC method with fluorescence detection. The mean T max of metoprolol after the S, M, F (4.43, 4.00, 3.14 h, respectively) was found to be different ( P < 0.05) as compared to the OS (2.07 h). The ratio of α‐hydroxymetoprolol/metoprolol was higher for the OS (1.26) vs. the S, M, and F (1.02, 0.96, 0.99). The S/R enantiomer ratios of the concentration for metoprolol, ACMB, and α‐hydroxmetoprolol were calculated at each time point and showed a significant difference ( P < 0.05) in the absorption phase (1–4 h) vs. terminal phase (8–16 h) for fast input (solution and fast extended release formulations). Based on these results, it would appear that input rate influences the pharmacokinetics of metoprolol, its metabolites, and their enantiomers. Chirality 14:297–304, 2002. © 2002 Wiley‐Liss, Inc.